The tomato pathogenic fungus Fusarium oxysporum forma specialis lycopersisci (Fol) posses a two-partite genome. Eleven of the 15 chromosomes of the sequenced strain (Fol4287) are syntenic with chromosomes of the sister species Fusarium verticilloides and the more distantly related Fusarium graminearum, displaying high sequence similarity and conservation of gene order [1]. These core chromosomes contain all housekeeping genes and few transposable elements (TEs). Additionally, Fol4287 possesses four chromosomes that are devoid of housekeeping genes and accommodate 74% of the whole genome TE content and 95% of the class II TEs (DNA transposons). The four chromosomes and two smaller regions at the ends of two core chromosomes comprise the lineage-specific (LS) part of the Fol genome. The genes encoded in LS regions differ in their phylogenetic history from the genes on the core chromosomes [1, 2]. The term lineage-specific (LS) reflects the largely clonal structure of the Fo species complex. Fo reproduces asexually and consists of many clonal lineages, which, if pathogenic, are grouped into host-specific formae speciales (ff. spp.) [3]. While some ff. spp. are monophyletic, others are composed of several clonal lineages that appear to have independently acquired the ability to infect the same host plant [46]. This polyphyletic origin was likely caused by horizontal transfer of chromosomes encoding host specific virulence genes between Fo lineages, thereby allowing the distinction of members of a f. sp., not by overall genetic relatedness, but by the presence or absence of certain LS chromosomes [1].

In Fol, one LS chromosome (chromosome 14 of Fol4287) largely defines the pathogenic phenotype of this f. sp., i.e. the ability to cause wilt disease in tomato. Horizontal transfer of this pathogenicity chromosome from a tomato pathogenic isolate to a non-pathogenic isolate during co-cultivation resulted in novel tomato-pathogenic lineages, demonstrating that it contains genes that promote infection of tomato [1]. Among these genes are all known Fol4287 effector genes called SIX (Secreted In Xylem) genes. Like many other plant pathogens, Fol utilizes small, secreted proteins to promote virulence by manipulating its plant host and suppressing host defense responses, typically through interaction with host proteins [7, 8]. Six proteins are small, commonly cysteine-rich, lack homology to other proteins and have a signal peptide for secretion [8]. Six of the seven previously described Six proteins are encoded on the pathogenicity chromosome; the genomic location of SIX4, whose gene product is recognized by the tomato resistance proteins I and I-1, is unknown because it is not present in the sequenced race 2 isolate Fol4287. Although SIX genes were likely acquired by horizontal transfer of the pathogenicity chromosome, they are not functionally independent of the core genome. Their expression requires the transcription factor Sge1 (SIX gene expression 1), which is encoded on a core chromosome [9]. It is unknown whether Sge1 regulates SIX gene expression directly or indirectly, for example through the action of other transcription factors.

Effector genes in other plant pathogens, such as Magnoporthe oryzae, Leptosphaeria maculans or Phythophthora infestans, are also found proximal to TEs and TEs have been proposed as the underlying agents that provide a plastic environment for the emergence of new virulence traits [1012]. The potential of TEs to affect genome structure is a consequence of both their mobility and their inherent structure. Generally, two different TE classes are distinguished by their transposition intermediate: RNA or DNA. Class I TEs (or retrotransposons) transpose via a “copy-paste mechanism” by copying themselves into an RNA-intermediate before inserting at a new site, while class II TEs (or DNA transposons) leave the donor site to reintegrate at another site via a “cut-paste mechanism”, although the original copy can also be retained [13]. Class I TEs are either flanked by terminal inverted repeats (TIRs), long terminal repeats (LTRs) or simple non-coding regions. Class II TEs are usually flanked by TIRs [14]. Special TE families are the MITEs (Miniature Inverted-repeat Tranposable Elements), non-autonomous class II TEs of short length, which are thought to have evolved from autonomous TEs by deletion of their transposase ORF [15]. Recombination between identical or highly similar TEs can cause structural rearrangements like deletions, inversions, duplications and translocations depending on the orientation and genomic location of the recombining TE members [16]. For an asexual fungus like Fol, TE-mediated recombination might represent a mechanism to create genetic variation in the absence of meiotic recombination. Next to gross structural rearrangements, TEs also contribute to evolution of novel phenotypes by transposition into new sites. For example, insertion of the hAT transposase Drifter into the coding sequence of an ancestral SIX1 homolog (SIX1-H) disrupted the open-reading frame (ORFs) of SIX1-H, thus creating an effector pseudogene [8]. In another case, insertion of a Hornet-like transposon at the SIX4 locus of a japanese race 3 Fol isolate created a fusion protein, which was no longer recognized by the corresponding I-1 tomato resistance protein [17]. TE insertion might also influence gene expression when it occurs within a promoter.

To further our understanding of the molecular basis of pathogenicity of Fol towards tomato, we conducted a detailed annotation of the predicted proteins encoded by the Fol pathogenicity chromosome. In addition, to advance our understanding of the potential role of the genomic context of effector genes in gene evolution or expression, we also annotated TEs on this chromosome. We thus obtained a detailed picture of the genomic landscape of the pathogenicity chromosome. Within this TE-rich landscape, we recognized mini-clusters of SIX genes. SIX genes are associated with two MITEs: a mimp upstream in all cases and, frequently, an mFot5 downstream. Using promoter deletions at two SIX gene loci, we studied the influence of the mimp on SIX gene expression. Finally, we were able to exploit the consistent presence of a mimp in the promoters of SIX genes and other virulence-associated genes to develop a method to identify candidate effector genes in F. oxysporum.


Non-TE genes on the Folpathogenicity chromosome group into a small set of functional classes

Non-TE ORFs occupy only 13% of the DNA space on the pathogenicity chromosome of Fol, which consists of four supercontigs (sc) (sc 22, 36, 43, 51) in the most recent Fol genome assembly (Li-Jun Ma, personal communication, Table 1). Most of the manually curated 245 non-TE ORFs on this chromosome encode proteins of unknown function, which are annotated as hypothetical proteins or proteins with domains of unknown function (140 ORFs, Figure 1). Some of these unknown proteins have homologous sequences in F. oxysporum or in other fungi (Additional file 1). Two functional groups stand out among the predicted products of the remaining 103 non-TE ORFs: secreted proteins (29) and proteins involved in secondary metabolism (35). Other functional groups include transcription factors (11), proteins with nucleic acid related functions (10), heterokaryon incompatibility (Het) proteins (4), transporters (3), cyclins (3) and other intracellular functions (17), such as GTPases and protein kinases (Figure 1). As reported by Ma et al., there are no genes for housekeeping proteins on the pathogenicity chromosome [1]. Among the predicted secreted proteins, we find nine secreted enzymes, such as oxidoreductase, chitinase and glucanase, and 20 secreted proteins of unknown function. Sixteen of the latter encode proteins smaller than 300 amino acids. Among those are the previously described effector genes SIX1, SIX2, SIX3, SIX5, SIX6 and SIX7[1820]. Proteins encoded on the Fol pathogenicity chromosome that are likely involved in secondary metabolism [1] include methyl transferases (6), cytochrome P450s (6) and glycosyltransferases (3). A putative secondary metabolite gene cluster on sc51 includes genes for three cytochrome P450s, a glycosyltransferase, a methyltransferase, a squalene-hopene cyclase and a homolog of Tri7, an acetyltransferase that is part of the trichothecene gene cluster in Gibberella zeae[21]. The genes in this putative secondary metabolite cluster are expressed during tomato infection (Additional file 2) and might therefore be important for pathogenicity of the fungus.

Table 1 Space occupied by TEs and non-TE ORFs on the pathogenicity chromosome
Figure 1
figure 1

TEs dominate on the pathogenicity chromosome. TEs and non-TE genes are presented as percentage of the total TE/gene content. Genes coding for secreted proteins (including SIX genes) constitute one of the best-represented classes.

Currently, it is not known how F. oxysporum can transfer chromosomes horizontally from one strain to another. One hypothesis is that horizontal chromosome transfer (HCT) occurs via anastomosis tubes – specialized, unbranched tubes that connect conidia or hyphae [2, 22]. Anastomosis tubes result in heterokaryon formation between two fungal individuals [23]. This heterokaryon is only viable if the individuals have the same HET (Heterokaryon incompatibility) genotype; otherwise it undergoes a characteristic cell death reaction called an incompatibility reaction [24]. Four genes on the pathogenicity chromosome encode proteins with similarity to Het proteins in other fungi (FOXG_14188, FOXG_14292, FOXG_14283, FOXG_14284). Het proteins like Het-E from Podospora anserina often harbor NACHT (NAIP, CIIA, HET-E, TP1) domains, or a highly divergent nucleoside phosphorylase (Pfs) linked with protein-binding modules such as Ankyrin repeats [25]. FOXG_14188 encodes a protein with a NACHT domain, FOXG_14292 a protein with a Pfs domain and Ankyrin repeats, FOXG_14283 a protein with a Pfs, an ATPase and Ankyrin repeats and FOXG_14284 a protein with Pfs and Ankyrin repeats (Additional file 1). The presence of HET-like genes on the pathogenicity chromosome may be seen to contradict HCT via anastomosis tubes, because additional HET loci would raise the chance of incompatibility between strains, involving programmed cell death of fused compartments. On the other hand, incompatibility does not appear to be a barrier to HCT [1]. Moreover, we do not know whether the HET-like genes on the pathogenicity chromosome are really involved in incompatibility.

Since transfer of the pathogenicity chromosome is sufficient to confer pathogenicity towards tomato, the virulence genes on it must be expressed in the new host strain. We know that there is crosstalk between the core and pathogenicity chromosome, because the core chromosome-encoded Sge1 controls SIX gene expression [26]. The presence of eleven genes encoding transcription factors on the pathogenicity chromosome suggests that transcription of genes on the pathogenicity chromosome may also be controlled by the chromosome itself. Among the transcription factors encoded on the pathogenicity chromosome are three copies of FTF1, which is induced upon plant infection [27], suggesting that at least a subset of the transcription factors encoded on the pathogenicity chromosome may be required for transcriptional reprogramming during plant infection.

Next to transcription factors, nine other genes encode proteins with nucleic acid-related functions (Figure 1). Most of these proteins are predicted to function in structural rearrangements of DNA or in chromatin modifications. FOXG_16427 encodes a poly(ADP)-ribose polymerase (Parp1) which binds to damaged or single-stranded DNA to recruit DNA repairing enzymes [28]. Other genes encode putative components of the RNA silencing machinery, including closely spaced genes for an RNA-dependent RNA polymerase (FOXG_16453), an RNA interference and gene silencing protein (FOXG_16455) and a RNaseH domain-containing protein (FOXG_16456). FOXG_14161 encodes a protein homologous to the eukaryotic conserved kinetochore protein Mis12 that is involved correct segregation of daughter chromatids during mitosis and meiosis [29]. FOXG_14165 encodes a protein with a BAH (bromo-adjacent homology) domain which may interact with gene silencing components [30]. Similarly, FOXG_14186 encodes a chromodomain protein that typically recruits protein complexes to chromatin and reads the epigenetic code by recognizing lysine methylation [31]. Proteins involved in chromatin modification and RNA interference might influence gene expression during pathogenicity.

The Folpathogenicity chromosome harbours a large diversity of transposable elements

To exhaustively identify TEs and TE relics on the Fol pathogenicity chromosome, we performed a self-BLASTN of the genome sequence, then identified multi-copy sequences and sorted them into non-redundant families. Secondly, we looked for inverted repeats (IRs) of at least 19 bp encompassing at most 5 kb of sequence. This expanded the set of identified TEs relative to an initial survey [1]. Taken together, TEs occupy about twice as much (24%) chromosomal DNA space as non-TE ORFs (13%, Table 1).

Both Class I and Class II TEs (full length and fragments) are present in approximately equal numbers (266 Class I, 249 class II, Table 2) on the pathogenicity chromosome, which is surprising because retrotransposons often dominate the TE fraction of a given genome [11, 3234]. For annotation of the TE classes we followed the classification system proposed by Wicker and colleagues that comprises both mechanistic and enzymatic criteria [14]. Class I TEs all transpose by transcribing themselves into an RNA intermediate, then reverse-transcribing the RNA by a TE-encoded reverse transcriptase and inserting into a new genomic region. There are three orders of class I TEs: Long-terminal-repeat (LTR) TEs, long-interspersed nuclear elements (LINE) and short interspersed nuclear elements (SINE).

Table 2 Transposable elements on the Fol4287 pathogenicity chromosome

LTR retrotransposons are similar to retroviruses and encode multiple enzymatic domains including Gag (a viral coat protein), protease, RNaseH, reverse transcriptase and integrase, flanked by long terminal repeats [14]. Within the LTR order we identified members of the Gypsy/Ty3 (27) and Copia/Ty1 (59) superfamilies, a novel class I TE named Yaret2, which encodes integrase (IPR001584), RNaseH (IPR012337), reverse transcriptase (IPR013103) and a Zinc-finger (IPR001878) domain, as well as two novel solo-LTR families. Solo-LTRs can be the result of intrachromosomal or intraelement recombination between the LTRs, thereby removing the internal domains and creating a solo LTR at the excision site [35]. Several of these LTR transposons have been previously recognized in Fo or in other pathogenic fungi. Nht2, for example, is also present on a LS chromosome of Fusarium solani[36].

LINE elements lack the LTRs that are characteristic for the retroviral-like class I TEs. In this order we identified 31 MGR583-like elements and 34 Yaret1 and Yaret1-like elements (24 and 10, respectively). MGR583 accompanies the effector gene AVR-PITA in some M. oryzae isolates [12]. The latter two are novel LINEs. Foxy (32 copies) represents the only TE of the SINE class on the pathogenicity chromosome. Foxy appears to be an active TE that is specific for Fusarium species [37]. Foxy elements are the most abundant class I TEs in Fol and they are evenly distributed over the pathogenicity chromosome and also throughout core chromosomes [1, 38] (this manuscript). This dispersed distribution pattern is also apparent for the other class I TEs. Finally, we detected 10 copies of Marsu, which is a retrotransposon that cannot be classified as LTR, LINE or SINE. Copies of Marsu were first described in Fo f. sp. phaseoli where they were found downstream of the FTF1 gene [27]. Ramos et al. speculated that the Marsu element might be responsible for gene duplication events of FTF1[27]. For most retrotransposon classes on the pathogenicity chromosome, we find only few full-length copies. Marsu is the marked exception: seven of the ten copies are full-length. Marsu copies are present in other Fol4287 LS regions, and two copies reside on core chromosomes. Although we did not detect identical copies within the genome sequence of Fol4287, the presence of moderately divergent copies and many full-length copies suggest that Marsu elements have been active relatively recently.

Compared to class I elements, class II elements are less evenly distributed on the chromosome and many aggregate in large chromosomal subregions (Figure 2). Class II elements are divided into two subclasses. Among subclass I we identified one Crypton copy. Cryptons encode a tyrosine-recombinase to cut and rejoin recombining DNA strands. They were first identified in human pathogenic fungi and were later found to be domesticated in vertebrates [39, 40]. There are more Crypton copies present on other LS chromosomes, but none on core chromosomes. Within subclass II we identified nine Helitron copies. Helitrons are unusual class II TE; instead of a ‘cut and paste’ mechanism they transpose via a rolling-circle mechanism [14]. With this transposition mechanism they often capture host genes and thus contribute to genome evolution [15]. At least eight of the nine Helitron copies on the pathogenicity chromosome are intact; one is truncated by a sequence gap (Additional file 1). All copies are 99-100% identical in sequence, and there are intact Helitron copies on core chromosomes, suggesting that Helitrons are still active.

Figure 2
figure 2

SIX genes reside in class II TE-enriched chromosomal subregions. TE densities and SIX gene locations were displayed in the IGV Genome Browser. Supercontigs are ordered according to their position in the optical map of chromosome 14, ignoring gaps between them. The positions of the SIX genes are indicated by stars. Numbers above the enlarged windows refer to position (kb) in the respective supercontig (sc).

The best-represented order of class II TEs are the Terminal Inverted Repeat (TIR) TEs (Table 2). These TEs consists of a transposase ORF flanked by TIRs [14]. Among the TC1/mariner superfamily, we found multiple, diverse Fot lineages belonging to the pogo family. This finding confirms the previously shown preferred localization of pogo elements on LS chromosomes [41]. We observed a similar diversification of Hop elements belonging to the Mutator family. Five Hop classes are present with one to 13 copies, most of which are not full-length, although Hop has been shown to be active in Fo[42]. Most TE families, including three Folyt copies and 16 Hornet copies, belong to the hAT family. Folyt has been identified as an expressed and active transposable element in Fol by transposon trapping [43]. Hornet1 was discovered during analysis of transposons in Fo f. sp. melonis[44]. The only copy of the hAT transposon Drifter adjoins the truncated effector gene SIX1-H[45]. Overall, as previously shown for some genomic regions in Fom, class II TEs seem to preferentially insert into or close to each other, creating class II TE-enriched subregions on the Fol pathogenicity chromosome.

These subregions are also enriched for MITEs. MITEs are non-autonomous TEs, which basically consist of TIRs flanking a short non-coding DNA sequence. Three different classes of MITEs are present on the pathogenicity chromosome: 55 mimps (miniature Impalas), three Gimlis and 14 mFot5s (of which one is interrupted by a retrotransposon). MITEs require an associated transposase for transposition. Often, this associated transposase has similar TIRs [15]. For mFot5 transposition, two TEs encoding intact Fot5 transposases on the pathogenicity chromosome might facilitate transposition. Mimps are transposed by the Impala transposase, which was shown to be active in the melon pathogenic strain Fo f. sp. melonis by transposon tagging [46, 47]. However, in Fol4287 all three Impala copies, which reside on the pathogenicity chromosome, do not encode a full-length transposase, suggesting that mimps are presently not actively transposed in Fol4287. The large diversification of the mimp lineages with members of more than four families and without two identical copies also suggests that mimps are not presently active in Fol4287.

Mimps are associated with promoters of SIXgenes

SIX genes tend to reside in chromosomal subregions that are enriched for class II TEs, sometimes as mini-clusters (Figure 2, Additional file 1). For example, SIX1 and SIX2 form a mini-cluster with one intervening gene (salicylate hydrolase homolog (SSH1)) and two intervening mimps, flanked by another mimp and a Fot5 (Figure 3, see below). SIX3 and SIX5 form another mini-cluster with an intervening mimp, with nearby mFot5 and Fot5 fragments. This mini-cluster is flanked on both sides by inverted repeats, suggesting that this mini-cluster might be able to be transposed (Figure 3, Additional file 1).

Figure 3
figure 3

Details of two class II TE-enriched chromosomal subregions with SIX gene mini-clusters. Schematic representations of two equally large regions of the Fol4287 pathogenicity chromosome: (A) part of supercontig 2.36 and (B) supercontig 2.51. Numbers represent FOXG gene numbers. Italic descriptions highlight interesting genes as reference points. Boxes indicate the telomeric repeat region and the putative secondary metabolite gene cluster. The genomic maps were drawn to scale.

A closer inspection of the SIX gene promoters, which we pragmatically define as 1500 bp upstream of the start codon, revealed the presence of a mimp in the promoters of SIX1, SIX2, SIX3, SIX5, SIX6 and SIX7 (Figure 4). The mimp in the SIX1 locus was revealed by re-sequencing, because in the Fol4287 genome assembly there is a sequence gap upstream of the SIX1 ORF. Another sequence gap separates a mimp from SIX7. We were not able to bridge this gap by PCR and therefore cannot rule out that the distance between the mimp and SIX7 is bigger than 1.5 kb or that there is another mimp present that is closer to the SIX7 start codon. The avirulence gene SIX4/AVR1 of race 1 Fol strains, which is not present in Fol 4287 (race 2), also harbors a mimp in its promoter sequence (Figure 4). The pathogenicity chromosome harbors more than half of the mimps present in the Fol4287 genome (Table 3). The other copies are mainly present on the three other LS chromosomes with the exception of four mimps on core chromosomes, as observed before [48]. Only a subset of the mimps on the pathogenicity chromosome is present in putative promoters (i.e. within 1500 bp of a predicted start codon). While SIX1-7 all harbor a mimp in their promoter, only 8.3% of all annotated non-TE ORFs on the pathogenicity chromosome do so. This association of mimps with SIX gene promoters is highly significant (chi-square test p = 5.25E-16 for association by chance of mimps with the six known SIX genes on the Fol4287 pathogenicity chromosome). Additional annotated ORFs with a mimp in the promoter region encode a bZIP transcription factor, an integral membrane protein, an alpha-N glucosaminetransferase, the Ftf1 transcription factor (2 copies), a catalase-peroxidase, the oxidoreductase Orx1, a homolog of the Verticillium dahliae avirulence protein Ave1, a methyltransferase, a cytochrome P450 and a squalene-hopene cyclase. The latter three genes belong to the putative secondary metabolite cluster that is co-expressed during plant infection (see above). Likewise, FTF1 has previously been shown to be expressed during plant infection [27]. The catalase-peroxidase and Orx1 are secreted in the xylem sap of Fol-infected tomato plants [19] (this manuscript). Overall, therefore, mimps seem to be preferentially associated with the promoters of genes that are expressed during plant infection.

Figure 4
figure 4

SIX genes harbor a mimp in their promoter. SIX gene loci including 1500 bp up-and downstream of the SIX ORF are drawn to scale. A miniature Impala (mimp, pink box) is present in the promoters of SIX1 – SIX3 and SIX5 – SIX7 in Fol4287 (race 2 isolate). The SIX4 locus (boxed) is not present in the race 2 isolate. It was sequenced and analyzed in the race 1 isolate Fol004. Downstream of some SIX genes is another MITE, mFot5 (dark blue box). Inverted repeats (IR) flanking the SIX3/SIX5 locus are represented by thick black lines.

Table 3 Distribution of mimps in the Fol4287 genome

To see whether additional, potentially regulatory elements may be enriched in SIX gene promoters, we analyzed the promoter sequences of SIX1, SIX2, SIX3, SIX5, SIX6 and SIX7 for enriched k-mers. Several overlapping 6 to 9mers were significantly enriched within these promoters. The most frequent of these form the sequence TCGGCAGTT (see Methods for details). Perfect matches to this sequence are present in the SIX1 and SIX3/SIX5 promoters. Compared to the entire gene set of the Fol4287 genome, the association between the presence of at least one or two of the 6mers TCGGCA, GGCAGT and the 7mer GGCAGTT and the 1000 bp upstream region of effector genes appears to be significant (Additional file 3).

Finally, we also examined the 1500 bp downstream of the STOP codons of SIX genes. mFot5 is present downstream of SIX2, SIX4, SIX5 and SIX7 (Figure 4). The association of this MITE with the SIX genes is weaker than the mimp association with the SIX gene promoters, because it is not present downstream of all the SIX genes on the pathogenicity chromosome.

SIX1gene expression is not dependent on the presence of a mimp in the promoter

We next wanted to know whether the mimp or the putative regulatory elements enriched in the SIX gene promoters are directly involved in transcriptional regulation of the SIX genes. To test this, we designed two constructs to replace different parts of the SIX1 promoter with a hygromycin resistance cassette. Both deletion constructs included the mimp, the difference between the constructs being that the SIX1p1189 construct (1552 to 363bp upstream of the translation start site) deletes only three of the six conserved SIX gene promoter 12 mers, while the SIX1p1230 construct (-1552 bp to -323 bp) deletes five of these 12 mers (Figure 5A).

Figure 5
figure 5

Deletion of the mimp in the SIX1 promoter does not impair SIX1 expression, but a small region with a conserved motif is required for SIX1 expression during plant infection. (A) Schematic representation of the SIX1 locus. Black lines: deleted promoter fragments (deletion length in bp); pink box: mimp; yellow arrow: SIX gene; orange circles: sequence matching AAGTCGGCAGTT[AG] motif enriched in SIX1-7 promoters. (B) In vitro expression of SIX1 in the promoter deletion strains. Mycelium of the indicated Fol strains was collected after growth in minimal medium, From the collected mycelium RNA was extracted and RT-PCR was performed to detect transcripts of SIX1 and, as control, the constitutively expressed FEM gene. (C) In planta expression of SIX1 in the promoter deletion strains. Ten days old susceptible (without resistance genes) or resistant (encoding the I-3 resistance protein that recognizes Six1) tomato seedlings were inoculated with the indicated Fol strains or with water (mock). Roots were harvested 9 dpi (days post inoculation, RNA was extracted and RT-PCR was performed as described above. (D) Disease assay of tomato plants. Ten days old seedlings of susceptible or resistant tomato seedlings (as above) were inoculated with the indicated strains or with water. Three weeks after inoculation disease was scored by determining the plant weight above the cotyledons and by phenotypic scoring according to a disease index ranging from zero (no disease) to four (heavily diseased or dead plants). (1) mock, (2) WT, (3) SIX1p1189#1, (4) SIX1p1189#2, (5) SIX1p1230#1, (6) SIX1p1230#2. Please note that, SIX1p1189#1 was not included in the bioassay with the resistant cultivar, because it is not pathogenic (see D). A black box marks interactions where recognition of Six1 by I-3 is broken or where no disease is caused. Error bars indicate the 95% confidence interval of the mean.

First, we tested whether SIX1 was still expressed in the promoter deletion strains in vitro. Most SIX genes are not highly expressed in vitro, their expression is only switched on upon plant infection. However, a low amount of SIX1 transcript is detectable in vitro[26]. To our surprise, SIX1 was expressed in both SIX1p1189 and SIX3p1230 promoter deletion strains despite the absence of a large part of the SIX1 upstream region (Figure 5B).

Six1 is recognized by the tomato resistance protein I-3 and triggers disease resistance in tomato plants carrying the I-3-gene, thereby prohibiting extensive fungal infection [49]. Upon plant infection, SIX1 was only expressed from strains with the shorter SIX1p1189 deletion in both susceptible and resistant tomato cultivars. All transformed strains remained pathogenic towards tomato without Fol resistance genes, indicating that they were not affected in pathogenicity (Figure 5D). Consistent with the in planta expression pattern, only the wild type and strains with the SIX1p1189 promoter deletion were avirulent on the resistant tomato cultivar. In contrast, I-3 tomato cultivars that were infected with Fol strains carrying the SIX3p1230 promoter deletion were diseased, indicating the absence or reduced accumulation of the Six1 avirulence protein (Figure 5D). Taken together, deletion of the mimp did not impair SIX1 expression in vitro or in in planta and this mimp is therefore not required for transcriptional regulation of the SIX1 gene. However, a promoter region including two TCGGCA elements appears to be required for SIX1 expression during plant infection.

SIX3/SIX5promoter deletions reveal complex regulation at this locus

To further investigate the functional role of mimps in effector gene expression, we also designed promoter deletion constructs for the SIX3-SIX5 locus. SIX3 and SIX5 share the same 1365 bp upstream sequence. This bidirectional promoter allowed us to test the expression of two different SIX genes with the same promoter deletion constructs. Like SIX1, SIX3 is also recognized by a tomato resistance protein, I-2 in this case, and expression of SIX3 and SIX5 is low but detectable in vitro[18, 26]. We designed three promoter deletion constructs: SIX3p539 (1095 to 520 bp upstream of the transcription start site), SIX3p807 (-1095 to -252 bp) and SIX3p859 (-1059 to -200 bp). SIX3p539 deletes six of the nine TCGGCA elements, but does not include the mimp, SIX3p807 includes the six TCGGCA elements and the mimp and SIX3p859 additionally deletes one more TCGGCA element (Figure 6A). Again, none of these promoter deletions impairs expression of SIX3 or SIX5 in vitro (Figure 6B). During plant infection, a reduced level of SIX3 mRNA was detected in Fol strains carrying the SIX3p539 deletion, but not in strains with the SIX3p807 deletion. SIX5 is not expressed in either SIX3p539 or SIX3p807 deletion strains (Figure 6C). Remarkably, both SIX3 and SIX5 are expressed during plant infection in Fol strains carrying the most extensive promoter deletion, SIX3p859 (Figure 6C). With one exception, all tested strains were still able to cause disease on susceptible tomato cultivars and are thus not generally impaired in pathogenicity (Figure 6D). Only strains with the SIX3p859 deletion trigger a resistance response in tomato plants carrying the I-2 resistance gene, while the Fol strains with the SIX3p539and SIX3p807 promoter deletions break I-2-mediated resistance, consistent with the Six3 protein not being produced by these strains (Figure 6C). Although in the Fol strains carrying the SIX3p539 promoter deletion a residual amount of SIX3 transcript is present, these strains are virulent. This may be explained by the additional requirement of SIX5 for I-2-mediated resistance (manuscript in preparation).

Figure 6
figure 6

Deletion of the mimp in the shared promoter region of SIX3 and SIX5 does not affect expression of the two genes. (A) Schematic representation of the SIX3/SIX5 locus. Black lines: deleted promoter fragments (length of the deletion in bp; pink box: mimp; yellow arrow: SIX gene; orange circles: sequence matching AAGTCGGCAGTT[AG] motif, which is enriched in SIX1-7 promoters. (B) In vitro expression of SIX3 and SIX5 in the promoter deletion strains. Mycelium of the indicated Fol strains was collected after growth in minimal medium, RNA was extracted and RT-PCR was performed. (C) In planta expression of SIX3 and SIX5 in the promoter deletion strains. Roots of ten days old susceptible (without resistance genes) or resistant (encoding the I-2 resistance protein that recognizes Six3) tomato seedlings were inoculated with the indicated Fol strains or with water (mock). Roots were harvested 9 dpi (days post inoculation), RNA was extracted and RT-PCR was performed as described above. Expression of SIX1 was used as a control. (D) Disease assay of tomato plants. Performed as above. Error bars indicate the 95% confidence interval of the mean. Numbers indicate the strains with which the tomato plants were inoculated: (1) mock, (2) Fol007 (WT), (3) SIX3p539#2, (4) SIX3p807#1, (5) SIX3p807#2, (6) SIX3p859#1, (7) SIX3p859#2. A black box marks interactions where recognition of Six3 by I-2 is broken or where no disease is caused.

From this set of experiments in two SIX gene loci, we can conclude that the mimps are not required for regulation of SIX gene expression. On the other hand, deletion of a short region containing a single TCGGCA element in the promoter of SIX1 abolishes SIX1 expression suggesting that this motif might represent a transcription factor-binding site (Figure 5C). In contrast, at the SIX3-SIX5 locus additional deletion of a region containing the same motif restores expression of both SIX3 and SIX5 during plant infection (Figure 6C).

The presence of mimps in the promoters of SIXgenes enables prediction of novel effector candidates

Next, we wanted to test whether we can use the consistent presence of a mimp in the upstream region of the SIX genes to predict novel effector candidates. We searched the Fol4287 genome for the presence of a mimp TIR within 2 kb upstream of an ORF encoding a protein with an N-terminal signal peptide for secretion (as defined by SignalP). We also analyzed the xylem sap proteome of Fol-infected tomato plants by mass spectrometry to see which of the predicted effectors are secreted by the fungus during plant infection.

By the in silico search for mimp-association we predicted 16 effector genes in Fol4287, which are located on chromosomes 3, 6 and 14. These include three of the known SIX genes on the pathogenicity chromosome: SIX2, SIX3, SIX6. SIX1 and SIX7 were not identified because of sequencing gaps in the Fol4287 genome assembly (see above). SIX5 is a small gene comprising three exons. The first exon is unusually short and ends directly after the encoded signal peptide for secretion. Therefore, SIX5 escaped signal peptide prediction (by SignalP) and thus was not identified with our approach.

Besides the known SIX genes, we identified nine genes coding for small secreted proteins and four genes coding for secreted enzymes with a mimp in the upstream region (Table 4). The latter comprise several multi-copy genes in the Fol4287 genome: two (non-identical) ORX1 copies, two copies of a gene coding for a catalase-peroxidase, two copies of a gene coding for a metalloprotease and three copies of a gene coding for an endo-polygalacturonase (Table 4). Both Orx1 and the catalase-peroxidase proteins were identified with mass spectrometry in the xylem sap of Fol-infected tomato plants, suggesting that they may play a role during plant infection.

Table 4 Novel effector candidates identified by searching for genes with a mimp IR in their promoter

Next to these two enzymes, we obtained protein sequences for four of the nine predicted effector proteins from the xylem sap proteome. Additionally, we identified three more small proteins in the xylem sap of infected tomato plants that were not predicted by our in silico search. We named the genes for which we found the protein products in xylem sap SIX8 - SIX14; one additional gene we named SIX8b for its high similarity to SIX8 (Table 4). Upon inspection of the regions upstream of their respective genes we could always identify a mimp. SIX8, SIX10 and SIX12 were not found with the in silico search because no signal peptide was detected. Similar to SIX5, SIX8 and SIX10 have a short first exon and therefore the signal peptide was not recognized by SignalP. SIX12 is an unusual effector gene: it does not encode a protein with a canonical signal peptide for secretion.

In contrast to the other SIX genes in Fol, SIX8 is not a single gene, but is present in two copies on the pathogenicity chromosome (sc36 and sc51) and in subtelomeric regions on chromosomes 2, 3 and 7 in a repeated block of around 7400 bp. This block includes incomplete copies of the class II TEs Marsu and YahAT7, a Foxy and a gene encoding an unknown protein (Figure 3, Additional file 1). The repeated sequences flanking the SIX8 genomic block on sc36 suggest that SIX8 is present in a subtelomeric region. Furthermore, two copies of a related gene, SIX8b, are present on chromosomes 3 and 6 each in the Fol4287 genome. In total, there are nine SIX8 and four SIX8b copies in the Fol4287 genome sequence. Both SIX8 and SIX8b appear to be preceded by a complex structure of (partial) mimps and mimp IRs (Additional file 4).

Like the SIX1-7 genes described above, the newly identified SIX genes, as well as several additional potential effector genes for which we did not find evidence for expression in planta, reside in class II TE-rich subregions (Figure 2, Table 4, Additional file 1). SIX11 resides in a region that includes SIX6, three genes coding for conserved secreted proteins, one gene for a MFS transporter and one for a fumarate reductase/succinate dehydrogenase, a FTF1 homolog and the ORX1 gene. SIX14 is part of a cluster containing SIX1, SSH1 and SIX2 (Figure 3). SIX10 and SIX12 make up a mini-cluster with SIX7. Similar to the SIX3/SIX5 mini-cluster, SIX12 is flanked on both sides by inverted repeats, suggesting that it may be mobilized by a transposase that recognizes these IRs. SIX13 (FOXG_17131 - 5 extended) is part of a duplicated region on chromosome 6 (sc 42), which is different from the interchromosomal duplication shared with chromosome 3.

Taken together, we have developed a method to predict novel effector genes in genomes of F. oxysporum based only on the following characteristics: (1) coding for small, secreted proteins, (2) harboring mimps or inverted repeats of mimps within 2 kb upstream of the start codon. We validated this method by mass spectrometric analysis of the xylem sap of Fol-infected tomato plants and confirmed in planta secretion of several predicted novel candidate effectors. These novel SIX genes represent ideal candidates for functional analysis.


Effector genes on the Folpathogenicity chromosome are associated with chromosomal subregions enriched in class II transposable elements

TEs dominate the Fol pathogenicity chromosome with large aggregates of class II TEs and more evenly distributed class I TEs. Interspersed within this TE-rich landscape are mostly single non-TE ORFs, a putative secondary metabolite cluster and the SIX gene mini-clusters. In many plant and fungal species with expanded genomes, retrotransposons are mainly responsible for genome expansion. Their mode of replication, which involves creating new copies during every transposition cycle, can rapidly increase genome size. Often, a single or few class I TEs account for the majority of TEs present in a genome. The maize genome, for example, consists of 76% class I TEs, with the Gypsy family element huck and the Copia element ji together accounting for nearly one quarter of the genome sequence [33]. Similarly, in the obligate fungal pathogen Blumeria graminis f. sp. hordei, the class I TE I (Line/Sine) alone occupies 17.2% of the entire genome space [32]. On the Fol pathogenicity chromosome, we do not observe such a massive expansion of retrotransposons. Instead, large aggregates of class II TEs are associated with genes involved in pathogenicity, such as the SIX gene mini-clusters. The tendency of class II TEs to concentrate in subchromosomal regions might result from recombination of their IRs with IRs of the same or a similar TE family. Occasionally, SIX genes might be trapped between the IRs and subsequently transposed together with the TE, resulting in the observed presence of SIX genes within class II TE-enriched chromosomal subregions. Support for this hypothesis stems from the observation that IRs directly flank SIX12 and the SIX3/SIX5 mini-cluster, although the transposase recognizing these IRs remains unknown. Similarly, the highly dynamic genomic location of the small, subtelomeric gene family AVR-Pita within the M. oryzae population has been attributed to the retrotransposons Inago-1 and Inago-2, which flank AVR-Pita. These are thought to be involved in multiple translocation events of AVR-Pita, thereby facilitating a cycle of loss and gain of recognition by rice cultivars encoding the cognate Pita resistance protein [12]. Next to retrotransposons, some DNA transposons have also been observed proximal to fungal effector genes. In Leptosphaeria maculans, putative effectors are clustered in AT-blocks together with three significantly over-represented TEs (one class I and two class II) [11]. Clustering of virulence genes might provide a selective advantage, because all captured genes experience the same genomic environment, e.g. an open or closed chromatin structure, thereby being simultaneously amenable for transcriptional regulation [50]. This might facilitate coordinated gene expression during plant infection.

MITEs and Folevolution

Mimps are always found within 1500 bp upstream the translation start site of SIX genes as well as upstream of several other genes that are expressed during plant infection. Mimps are uniformly small in size, ranging from 200 – 220 bp. Their central region has no coding capacity and is flanked by ~27 bp TIRs that resemble the TIRs of the Tc1/mariner transposase Impala [51]. Impalas have been shown to transpose mimps in a heterologous system [52]. However, none of the Impala copies in the Fol genome are intact, suggesting that mimps are not currently transposed in Fol4287. In the past there appear to have been several bursts of mimp amplification resulting in at least six mimp subfamilies present in Fol[51]. Strikingly, more than half of the mimps in Fol4287 are present on the pathogenicity chromosome and the other mimps, with four exceptions, are restricted to the LS regions (Table 3) [51].

mFot5s reside downstream of the SIX1/SSH1/SIX2, the SIX3/SIX5 and the SIX10/SIX12/SIX7 mini-clusters as well as downstream of the solo SIX9 gene (Figure 3, Additional file 1). mFot5 is also part of the putative secondary metabolite cluster that is co-expressed during Fol infection of tomato plants (Figure 3, Additional file 2). Downstream of SIX11 is no mFot5, but a full-length Fot5. The same is true for ORX1, which encodes an oxidoreductase that is secreted by Fol during tomato infection. mFot5 is a pogo-like MITE, less than 500 bp long with TIRs similar to those of the Fot5 transposon. In contrast to the lack of intact Impalas for mimp transposition, Fol4287 possesses around 64 intact Fot5 transposase ORFs that could mobilize mFot5s [41].

What could be the function of mimps in promoters of effector genes?

Strikingly, mimps are not only present in SIX gene promoters, but also in the promoters of several other genes that are expressed during plant infection. Among these are the gene for the oxidoreductase Orx1 and two genes of the presumptive secondary metabolite gene cluster. One possible scenario is that the mimp is a domesticated TE, which has adopted a function as transcription factor binding site, perhaps for Sge1, the transcription factor regulating SIX gene expression [26]. We tested this by deleting fragments of varying length in the promoter of SIX1 and the bidirectional, shared promoter of SIX3 and SIX5. In a strain in which the mimp in the promoter of SIX1 was deleted (Fol4287SIX1p1189), SIX1 expression in vitro and in planta was the same as in wild type. Likewise, SIX3 and SIX5 expression was not affected in a strain in which the mimp was absent in their shared upstream region (Fol4287SIX3p859). Therefore, we can rule out a direct involvement of the mimp in transcriptional regulation of SIX gene expression.

We did, however, observe that the presence or absence of other promoter regions affect gene expression at the SIX1 and the SIX3/SIX5 locus. By comparing two different promoter deletions, we found that SIX1 expression in planta requires a 41 bp region that includes one of the conserved TCGGCA elements that we found to be enriched in the SIX gene promoters (Figure 5). In contrast, SIX3 and SIX5 are not expressed from the two shorter promoter deletion strains, but expression of both genes is restored in the strain with the longest promoter deletion. The longest deletion additionally includes one of the TCGGCA elements (Figure 6A), which in this instance may mediate the action of a transcriptional repressor. The association of this element with upstream regions of effector genes is statistically significant (see Methods and Additional file 3 for details). Also, a perfect match to the extended motif (AAGTCGGCAGT) is present in the upstream regions of three genes encoding enzymes that we found in our analysis of the xylem sap proteome: FOXG_11769 on chromosome 10, encoding a glycosyl hydrolase and the closely related FOXG_14234 on the pathogenicity chromosome and FOXG_17180 on an unpositioned scaffold, encoding a peroxidase-catalases. Nevertheless, the function of this putative regulatory sequence remains to be established.

Interestingly, SIX1 as well as SIX3 and SIX5 were weakly expressed in all promoter deletion strains in vitro, but not in planta. In absence of a plant host, SIX gene expression is usually very low [26], while it is strongly induced upon plant infection [53]. SIX genes are only needed during plant infection; therefore the fungus might actively suppress SIX gene expression in the absence of a plant host. One way of suppressing gene expression is by modification of chromatin to a repressive, closed state. Repressive chromatin structures often involve histone modifications such as H3K9 methylation [54]. One origin of such repressive chromatin structures is TE silencing, often guided by small RNAs transcribed from the TE [55]. In plants of the Solanaceae family, MITEs proximal to R gene loci were shown to produce small RNAs that are recruiting the histone methylation machinery for TE silencing resulting in the formation of closed chromatin [56]. TE silencing of the MITEs surrounding the SIX genes might likewise create a repressive chromatin environment, which may serve as a first layer of SIX gene regulation. Upon stress, such as during plant infection, TEs might be derepressed as shown for the oomycete pathogen Phythophthora ramorum[57], thus creating an open chromatin structure. Binding of transcriptional activators or repressors would be possible in an open chromatin state and provide the basis for a second layer of regulation of SIX gene expression.

Identification of novel effector candidates

We identified eight novel (candidate) effector genes based on the presence of a mimp in their promoters and/or the presence of their protein product in xylem sap of infected plants. Five of these genes (SIX8b, SIX9, SIX11, SIX13, SIX14) were identified by the in silico search and validated by the analysis of xylem sap from infected tomato plants. Like the previously identified SIX1 and SIX7 genes, SIX10 escaped the in silico identification due to a sequencing gap close to its promoter. SIX12 encodes an unusual effector lacking a recognizable N-terminal signal peptide for secretion via the classic Endoplasmatic-Reticulum/Golgi route. Nevertheless, the Six12 protein is present in the xylem sap of infected tomato plants and therefore might be secreted via an unconventional protein secretion route [58]. SIX13 encodes the only effector known so far that is located on a LS chromosome other than the pathogenicity chromosome. We also identified FoAVE1 as a gene harboring a mimp in its promoter, but we did not detect the FoAve1 protein in the xylem sap nor detected FoAVE1 mRNA in infected plants (results not shown). Apparently, in the strains used here FoAVE1 is not expressed during infection, although it was shown to be able to elicit Ve1-mediated resistance in a heterologous system [59]. FoAve1 might be part of a silent effector reservoir together with the other three genes that encode small, secreted proteins and harbor a mimp in their promoters, but are not expressed during infection.

Some of the genes we identified here have been subject to gene or segmental duplications. ORX1 is present in two similar but not identical copies on the pathogenicity chromosome (FOXG_14258, FOXG_14236; Additional file 1). Two other genes, FOXG_17460 on the pathogenicity chromosome and FOXG_17130 on chromosome 6, both encode a metalloprotease. Apart from a missing 3’ end of FOXG_17460 due to a sequencing gap, the two genes and their promoters are identical, indicating a recent duplication event. SIX13 is also duplicated. In both cases the duplicated gene copies do not harbor a mimp in their promoter. SIX8b is present in four identical copies due to an intra- and interchromosomal segmental duplication within and between chromosome 3 and 6 [1]. This duplicated chromosomal segment corresponds to another small chromosome that can be transferred horizontally from the strain Fol007[1]. Progeny strains possessing both the pathogenicity chromosome and the other small chromosome are more aggressive towards tomato than progeny strains with only the pathogenicity chromosome. At present, we do not know which gene(s) on the small chromosome (corresponding to sc18 in the Fol4287 genome) contributes to pathogenicity towards tomato – Six8b was not found in the xylem sap proteome.

In summary, mimps are associated with the promoters of all small in planta secreted proteins, as well as several enzymes. Our strategy for in silico detection of effector genes in F. oxysporum is limited by three factors: 1) imperfect conservation of the IRs of a mimp, 2) sequencing gaps in the genome assembly and 3) absence of a canonical N-terminal signal peptide for secretion. The impact of first two factors may be alleviated by more advanced methods for mimp detection and genome assembly. The third factor, absence of a canonical signal peptide, can be either due to secretion via an unconventional route or to a failure of SignalP to predict a signal peptide, as was the case for SIX5 or SIX8. In the latter case, incorporation of gene structure (intron/exon) predictions or transcript sequences will be helpful. Overall, our approach presents a powerful tool to predict novel effectors and other virulence factors in F. oxysporum.


Class II TEs are much less evenly distributed over the Fol pathogenicity chromosome than class I TEs. Effector genes reside as single genes or mini-gene clusters within class II TE-enriched chromosomal subregions. Two MITEs are closely associated with effector genes. A (partial) mimp is always present in effector gene promoter regions and a mFot5 is frequently present downstream of the effector gene mini-clusters. We could exclude a direct involvement of the mimp in effector gene expression by making promoter deletion strains for two effector gene loci followed by gene expression analysis and tomato pathogenicity assays. Overall, the unique association of effector genes and mimps allowed us to develop a method to successfully predict candidate effector genes. For most of these genes, the corresponding protein was found by mass spectrometry in the xylem sap of tomato during Fol infection. Our method can easily be extended to predict novel effector genes in Fo strains with different host specificities.


Plant lines and fungal strains

The following tomato (Solanum lycopersicum) lines were used (Fol resistance genes between brackets): 90E402F (I-1) [60, 61]; 90E341F (I-2) [62] and E779 (I-3) [60], C32 (no I gene) [63]. The following Fol strains were used: Fol007 (race 2), Fol4287 (race 2), Fol004 (race1), Fol4287SIX1p1189, Fol4287SIX1p1230, Fol4287SIXc3p539, Fol4287SIX3p807, Fol4287SIX3p859, Fol4287Δsge1, Fol007Δsix1. See Rep et al. [45] for a more detailed description of the wild type Fol strains.

Identification and annotation of TEs

Repetitive DNA elements were identified by performing a self-BLASTN against the Fol4287 genome sequence, then using a custom PERL script (Amyott S.G. et al.,. manuscript in preparation), which identifies multi-copy sequences and sorts these repeated sequences into non-redundant families. Additional TEs with terminal inverted repeats were identified by search the Fol4287 genome for inverted repeats of at least 19 bp encompassing at most 5 kb of sequence. Blast was used to find all instances (full length or partial) in the Fol4287 genome. Additional file 5 contains prototypes for all newly identified TEs.

Promoter deletion constructs

The promoter deletion constructs for the SIX1 and SIX3/SIX5 promoters were made by PCR amplification sequences of the sequences flanking the part of the promoter that was to be deleted for homologous recombination, and their insertion in front of and behind the hygromycin resistance gene in the vector pRW2h (see below). For SIX1: for both deletion constructs a 829 bp upstream fragment was cloned into pRW2h [64] between the PacI and Acc65I sites and a1093 bp and 1052 bp downstream fragment, for the SIX1p1189 construct and the SIX1p1230 construct respectively, were cloned into pRW2h between at the XbaI site. For SIX3: a 1001 bp upstream fragment was cloned into pRW2h between the PacI and Acc651 sites and a 1332 bp (SIX3p539), a 1064 bp (SIX3p807) and a 1012 bp (SIX3p807) downstream fragment was cloned into the XbaI site of pRW2h. Transformation of these constructs to Fol4287 was done with Agrobacterium as described earlier [65].

Tomato disease assay

Ten days old tomato seedlings were inoculated with a fungal spore suspension and disease was scored after three weeks as described earlier [49]. The outcome of the disease assays was quantified in two ways: 1) average plant weight above the cotyledons and 2) phenotype scoring according to a disease index ranging from zero (no disease) to four (heavily diseased or dead) [49].

Folgene expression analysis

For in vitro expression analysis, Fol mycelium was harvested after three days growth at 25°C and 175 rpm in minimal growth medium (3% sucrose, 1% KNO3 and 0.17% yeast nitrogen base without amino acids and ammonia). For in planta expression analysis, ten days old tomato seedlings were inoculated with fungal spores suspensions as described above and roots were sampled eight or nine days after inoculation. From the collected material, RNA was isolated using TRIzol reagent (Gibco) followed by phenol-chloroform extraction. The isolated RNA was used to make cDNA using Promega Rnasin (ribonuclease inhibitor) and Gibco Superscript II RNaseH Reverse transcriptase according to the manufacturer’s instructions. Primers used for RT-PCR analysis are listed in Additional file 6.

Identification of novel effector candidates

Based on published sequences of prototypes of mimp1-4 as well as mimps present in promoters of SIX1-7, a consensus mimp 3’ IR was defined as ‘TT[TA]TTGCNNCCCACTG’. A PERL script was used to find instances of this pattern in the genome sequence of Fol4287, downloaded from the broad website ( For 150 of the 158 matches to this pattern, the next dinucleotide was ‘TA’, which is the required target site for mimps and Impalas.

For each mimp IR match, all open reading frames (ORFs) starting with an ATG and of at least 25 codons within 2000 bp downstream of the IR were selected. The ORFs were translated and the translation products submitted to signal peptide prediction by SignalP ( If positive, the instance was recorded (mimp IR sequence, translation product of ORF and their positions in the Fol4287 contig). The sequence surrounding this instance was retrieved and manually inspected to define the full ORF of the candidate effector gene.

In silicopromoter analysis

To find potential regulatory elements in promoters of effector genes, we first identified enriched k-mers in the concatenated upstream regions of SIX1, SIX2, SIX3, SIX5, SIX6 and SIX7, using Compseq ( As upstream regions we used here the sequences between the upstream mimp and the ATG, to avoid identification of sequences within mimps (especially the conserved inverted repeats). We looked for enriched 6mers, 7mers, 8mers and 9mers in both strands. Among the most frequent 6mers and 7mers, we found two classes: (1) A diversity of AT-sequences and (2) a small set of overlapping sequences that were present in one or more instances in all – or all but one – upstream regions. The most frequent sequence elements of the second class were the 6mers TCGGCA (16), GGCAGT (14), CGGCAG (11) and GCAGTT (11) and the 7mers GGCAGTT (11), TCGGCAG (9) and CGGCAGT (7). The overlap of these 6mers and 7mers is the 9mer TCGGCAGTT. This is also the most frequent 9mer, which occurs 6 times in the upstreams regions, namely in those of SIX1 (2X), SIX3 (1X) and SIX5 (3X). Except two palindromic AT-rich sequences (TTTTAAAA and TATATATA), the most frequent 8mers matched this 9mer: TCGGCAGT (6), CGGCAGTT (7), or extend it: GGCAGTTA (6). Two other frequent 8mers extend the sequence on the other end: AAGTCGGC (4) and AGTCGGCA (4). Additional overlapping, enriched 9mers (each occuring 3 times) further extend the combined sequence to the consensus AAGTCGGCAGTT[AG]A.

To assess the significance of the occurrence of this motif in the upstream regions of effector genes, we analysed the 17708 upstream regions of Fol4287 genes, defined as 1000 bp upstream of the predicted translational start codon. This analysis is summarized in Additional file 3. Briefly, we calculated the probability that the frequency with which the two most frequent (and overlapping) 6mers, TCGGCA and GGCAGT, and to the most frequent 7mer, GGCAGTT (a one base extension to the second 6mer), occur at least once or twice in the upstream regions of effector genes is by chance association. We did this both for the original set of effector genes used to find the pattern (SIX1-3 and SIX5-7), and for the entire set of identified effector genes (including SIX8b). All p values were lower than 0.05. The weakest association was between at least one TCGGCA element and the original set (p = 0.024) and between at least one GGCAGT and the entire set (p = 0.015). Association with at least twice occurences were more significant in all cases. Association with the entire set was slightly more significant for the TCGGCA element (at least once or at least twice) and for at least twice occurences of the GGCAGT element. The other associations were weaker with the entire set of effector genes.

Xylem sap collection, mass spectrometry and label free quantitative proteomics

Fol007 was used for tomato inoculation. Four-week-old tomato plants C32 were inoculated, after removing part of the root system, with a Fol spore suspension (5 × 106 spores mL−1) or with water as a negative control, and potted. Fourteen days post inoculation (dpi), xylem sap was collected as described [66, 67]. Briefly, stems were cut below the second true leaf and the plant was placed in a horizontal position. Then, for minimal 6 h sap bleeding from the cut surface was collected in tubes placed on ice. The collected xylem sap was stored at -20°C.

For label-free protein quantification 25 plants per inoculum were inoculated with Fol007 or water. Xylem sap was isolated as described above from four independent biological replicates. A fraction of the sap was used for immunoblotting, the remainder was concentrated with a Centricon plus-70 (Millipore) unit to a final volume of 200-300 μl. The protein concentration was determined with the bicinchoninic acid method (Sigma). After trichloroacetic acid/aceton precipitation protein isolated from inoculated plants with water or Fol007 was dissolved in sample buffer at equal concentration (1.5 μg/μl) and 30 μl per sample was loaded on the SDS-PAGE. SDS–PAGE was performed with Hoefer Mighty Small SE250 minigel equipment (Amersham Biosciences, AB, Uppsala). After a short run, the Coommassie PageBlue™ (Fermentas) was used to visualize the proteins in the SDS-PAGE. For each xylem sap sample one gel slice containing all proteins was cut from the Coomassie-stained gel. In-gel digestion was performed as described by Rep et al. [67]. The peptides obtained after this digestion were analyzed by nanoLC-MS/MS as described by Lu, et al [68]. Raw data from the LTQ-Orbitrap were analyzed with MaxQuant software [69, 70] to identify the proteins and allow label-free relative quantification. MaxQuant 1.1.36 settings were used according to the description by Peng, et al [71]. The Fol protein database used for the analysis was obtained from Fusarium Comparative Genome website ( and supplemented by adding the sequences of known Six proteins that are not annotated in the public database. A “contaminant” database was used that contains proteins such as trypsin and human keratins [71]. Bioinformatics analysis of the MaxQuant workflow and the statistical analysis of the abundances of the identified proteins were performed using Perseus (available at [70]. Only proteins identified with at least two peptides, of which one should be unique, were kept.