The association of homeobox gene expression with stem cell formation and morphogenesis in cultured Medicago truncatula
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Somatic embryogenesis (SE) is induced in vitro in Medicago truncatula 2HA by auxin and cytokinin but rarely in wild type Jemalong. The putative WUSCHEL (MtWUS), CLAVATA3 (MtCLV3) and the WUSCHEL-related homeobox gene WOX5 (MtWOX5) were investigated in M. truncatula (Mt) and identified by the similarity to Arabidopsis WUS, CLV3 and WOX5 in amino acid sequence, phylogeny and in planta and in vitro expression patterns. MtWUS was induced throughout embryogenic cultures by cytokinin after 24–48 h and maximum expression occurred after 1 week, which coincides with the induction of totipotent stem cells. During this period there was no MtCLV3 expression to suppress MtWUS. MtWUS expression, as illustrated by promoter-GUS studies, subsequently localised to the embryo, and there was then the onset of MtCLV3 expression. This suggests that the expression of the putative MtCLV3 coincides with the WUS-CLAVATA feedback loop becoming operational. RNAi studies showed that MtWUS expression is essential for callus and somatic embryo production. Based on the presence of MtWUS promoter binding sites, MtWUS may be required for the induction of MtSERF1, postulated to have a key role in the signalling required for SE induced in 2HA. MtWOX5 expressed in auxin-induced root primordia and root meristems and appears to be involved in pluripotent stem cell induction. The evidence is discussed that the homeobox genes MtWUS and MtWOX5 are “hijacked” for stem cell induction, which is key to somatic embryo and de novo root induction. In relation to SE, a role for WUS in the signalling involved in induction is discussed.
KeywordsMedicago Root development Somatic embryogenesis Stem cell formation WUSCHEL WUSCHEL-related homeobox genes
CLV3/endosperm surrounding region
Expressed sequence tag
Shoot apical meristem
The homeobox gene WUSCHEL (WUS) encodes a homeodomain transcription factor that has been shown to be a regulator of a pool of pluripotent stem cells in the apical meristem (Mayer et al. 1998; Bäurle and Laux 2005; Reddy and Meyerowitz 2005; Shani et al. 2006). Zuo et al. (2002) identified gain-of-function mutants, which caused somatic embryo formation in Arabidopsis in a range of tissues and organs. The responsible gene was found to be identical to WUS. Overexpression of WUS could induce somatic embryogenesis (SE). Zuo et al. (2002) concluded that WUS had a key role in the vegetative-to-embryogenic transition and in addition to having its well-known role in meristem development, could act as an embryo organiser. Gallois et al. (2004) have also investigated ectopic WUS expression and found that shoots could be induced in the roots and somatic embryos in the presence of auxin. This suggested that pluripotent or totipotent cells could be induced by WUS depending on the hormonal environment.
In the shoot meristem WUS expression is regulated by the small protein CLAVATA3 (CLV3) (Brand et al. 2000; Fiers et al. 2007). As the population of stem cells increases there is an increase in the synthesis and secretion of CLV3, which subsequently causes a decrease in the population of stem cells (Beveridge et al. 2007). CLV3 is proposed to bind to the CLV1/CLV2 receptor complex, initiating a signalling cascade, which leads to down-regulation of WUS expression in the cells of the organiser region of the apical meristem (Brand et al. 2000; Fiers et al. 2007; Ogawa et al. 2008). However there is no direct biochemical evidence for CLV3 interaction with a CLV1/CLV2 receptor complex as opposed to a CLV1/CLV1 complex. Müller et al. (2008) have evidence that the novel receptor kinase CORYNE and CLV2 may act together, and in parallel with CLV1 homodimers to perceive the CLV3 signal.
If overexpression of WUS can induce somatic embryos, then it would be expected that a similar result could be achieved by preventing the CLV signalling. Mordhorst et al. (1998), using the primordia timing (pt), clv1 and clv3 mutants and pt clv double mutants, found a correlation between increased shoot apical meristem size and an increased frequency of seedlings producing embryogenic seed lines.
There is a family of transcription factors related to WUS known as the WUSCHEL-related homeobox (WOX) gene family that includes WOX5 (Haecker et al. 2004). In Arabidopsis WOX5 is expressed in quiescent cells of the root apical meristem (Haecker et al. 2004). Stem cells surround the quiescent centre (Scheres 2005). Investigations by Sarkar et al. (2007) have shown that WOX5 acts to maintain the stem cells of the root apex and can be considered analogous to WUS that acts to maintain stem cells of the shoot apex. WOX5 expression occurs during in vitro root formation in cultured Medicago truncatula (Imin et al. 2007).
Medicago truncatula is a model legume (Rose 2008) that has been used to investigate the mechanisms of in vitro somatic embryo (Rose and Nolan 2006) and root formation (Rose et al. 2006; Imin et al. 2007). When leaf explants were cultured on basal medium with auxin and cytokinin, somatic embryos were induced and when cultured on basal medium plus auxin then roots were produced (Nolan et al. 2003).
The ability of plant cells to be directed into different developmental pathways in vitro provides systems that can be utilised to improve the understanding of plant stem cell biology. In this study we have further investigated the transcription factors WUSCHEL and WOX5 of M. truncatula that are important regulators of stem cell maintenance in vivo in relation to the induction of SE and root formation in vitro. The data obtained are consistent with a role for homeobox genes in the production of stem cells to produce either embryos or roots depending on the hormonal environment.
Materials and methods
The M. truncatula cultivars Jemalong 2HA (2HA) and wild type Jemalong were grown in standard potting mix under glasshouse conditions. 2HA is a highly embryogenic mutant of Jemalong produced in our laboratory (Rose et al. 1999). The nature of the mutation is not known. We have suggested that the difference between Jemalong and 2HA is likely to be epigenetic (Rose 2008). The wild type Jemalong used was an accession (SA1619) from the Australian National Medicago collection, South Australian Research and Development Institute (SARDI), Adelaide. Cultured M. truncatula leaf explants were obtained from glasshouse-grown plants.
Cultured leaf explants
The standard leaf culture procedure and media were as described by Nolan et al. (2003). Explants were cultured on P4 10:4 for 3 weeks before transfer to P4 10:4:1 (10 μM NAA, 4 μM BAP and 1 μM ABA added at 3 weeks). In some experiments 1 μM ABA was added at the beginning of culture in the P4 10:4:1 medium as we have found recently that this increases embryo number. Other treatments used 10 μM NAA alone or 4 μM BAP alone.
Sequence analysis and construction of phylogenetic trees
Multiple alignment analyses were performed with ClustalW using the Clustal 2.0.8 software in Clustal default colours. Phylogenetic trees were constructed using the bootstrap neighbour-joining method (1,000 rounds) (Saitou and Nei 1987) included in the Clustal 2.0.8 software. Phylogenetic trees were drawn using TreeView (Win32) 1.6.0 software (Page 1996).
Total RNA was isolated from intact leaves as a calibrator and from calli and other tissues, using the Qiagen RNeasy Plant Mini Prep Kit (Qiagen Pty Ltd, Doncaster, VIC, Australia) as per the manufacturer’s instructions. cDNA synthesis was performed using the Superscript II™ First-Strand Synthesis System for RT-PCR (Invitrogen, Carlsbad, CA, USA) starting with 1 μg of total RNA with oligo (dT)15 primers. Real-time PCR was performed using SYBR® GreenER™ qPCR SuperMix Universal Kit (Invitrogen) and analysed in the DNA Engine Opticon® 2 Continuous Fluorescence Detection System (Bio-Rad, Gladesville, NSW, Australia). Primers designed to quantify the expression levels for MtWUS were 5′-CTTACAACATTTCATCTGCTGGGCT-3′ (forward) and 5′-CGACATGATGACCAATCCATCCTAT-3′ (reverse), for MtWOX5 were 5′-CAAGCACTGATCAAATTCAGAAAAT-3′ (forward) and 5′-GAAAAAGCTCAAGAGTCTCAATCAC-3′ (reverse), and for MtCLV3 were 5′-ATGGCTTCTAAGTTCATCTTTTCTT-3′ (forward) and 5′-TCAAGGGTTTTCAGGCTTAATAGGG-3′ (reverse), which were normalised to those of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), primers 5′-TGGTCATCAAACCCTCAACA-3′ (forward) and 5′-CCTCGTTCTTTCCGCTATCA-3′ (reverse), in each sample every run. The tubes were then cycled at 94°C for 30 s, annealed at 60°C for 60 s, and extended at 72°C for 60 s. A melting curve was generated at the end of every run to ensure product uniformity. PCR reactions were performed in triplicate in at least two biological repeats. Transcript abundance was estimated using a modification of the comparative threshold cycle (Ct) method and was calculated as E−ΔΔCt, where ΔΔCt = (Cttarget − CtGAPDH)Time x − (Cttarget − CtGAPDH)Calibrator and E is the estimated amplification efficiency, which was calculated employing the linear regression method on the log(fluorescence) per cycle number data for each amplicon using the LinRegPCR software (Ramakers et al. 2003).
To generate the RNA probes, a 893-bp fragment of MtWUS was first amplified by PCR with the primers 5′-ATGGAACAGCCTCAACAACAACAA-3′ (forward) and 5′-GGTGACCTACAGCCGTAAGAGTTGA-3′ (reverse). Then, the promoter sequences of T7 and SP6 RNA polymerase were introduced to this fragment by a two-step PCR. The first primers used were 5′-GAGGCCGCGTATGGAACAGCCTCAACAACA-3′ (forward) and 5′-ACCCGGGGCTGGTGACCTACAGCCGTAAGA-3′ (reverse). The second set of primers used were 5′-TTATGTAATACGACTCACTATAGGGAGGCCGCGT-3′ (forward) and 5′-CCAATTTAGGTGACACTATAGAAGTACCCGGGGCT-3′ (reverse). For MtWOX5, a 659-bp fragment of full length cDNA sequence was first amplified by PCR with primers 5′-GTAAAAACATCTAGAATTGAAATATGG-3′ (forward) and 5′-TCCTAAACATTTTTCATATTATGCT-3′ (reverse). Sites for T7 and SP6 RNA polymerase were introduced through two-step PCR as for MtWUS. The first primers used were 5′-GAGGCCGCGTGTAAAAACATCTAGAATTGA-3′ (forward) and 5′-ACCCGGGGCTTCCTAAACATTTTTCATATT-3′ (reverse). The second set of primers was the same as for MtWUS. This PCR product was subsequently used as a template for in vitro transcription employing T7 and SP6 RNA polymerase to synthesise digoxigenin-labelled sense and anti-sense single-stranded RNA probes respectively using a DIG RNA Labelling Kit (Roche, Basel, Switzerland). Four- to five-week-old calli and other tissues were fixed in 4% formaldehyde in 0.025 M phosphate buffer at pH 7.2, dehydrated through an ethanol and ethanol: histolene (Fronine, Lomb Scientific, Taren Point, NSW, Australia) series, embedded in paraffin, sectioned, and hybridised with the digoxigenin-labelled sense and anti-sense probes as described previously (Mantiri et al. 2008a, b). The hybridisation was detected using a Fluorescent Antibody Enhancer Set for DIG detection (Roche) and was visualised as a red/purple colour after the NBT/BCIP colour reaction (Roche). Sense-strand probes were used as controls.
Construction of promoter-GUS fusions and inducible RNAi plasmids
For MtWUS promoter::GUS construction, a 3,182-bp fragment of promoter region was amplified by PCR with the primers 5′-CTAACTTCCGTTATCCGAGAATCTT-3′ (forward) and 5′-TGTTCCATGTTTTTGTTGGACTGAA-3′ (reverse). For MtWUS RNAi construction, a 204-bp fragment was amplified by PCR with the primers 5′-CTTACAACATTTCATCTGCTGGGCT-3′ (forward) and 5′-CGACATGATGACCAATCCATCCTAT-3′ (reverse). For MtWOX5 promoter::GUS construction, a 1,024-bp fragment of promoter region was amplified by PCR with the primers 5′-TTCCCAACATAATTTGTAACCTCAT-3′ (forward) and 5′-CATGCTCTCTTCCATATTTCAATTC-3′ (reverse). For the empty vector control, 88 bp of DNA was taken from the multiple cloning site of the vector pASK-IBA44, (5′-CCGGGGATCCCTCGAGGTCGACCTGCAGGGGGACCATGGTCTCAGGCCTGAGAGGATCGCATCACCATCACCATCACTAATAAGCTT-3′) (IBA, Göttingen, Germany). The gene-specific PCR products were cloned into the vector pCR8/GW/TOPO (Invitrogen). After extraction of the plasmids, the Gateway LR recombination reaction (Invitrogen) was carried out according to the manufacturer’s protocol to insert the gene-specific fragment into the binary T-DNA destination vector pMDC164 for promoter-GUS fusion constructs (Curtis and Grossniklaus 2003) or pOpOff2(hyg) (Wielopolska et al. 2005) for inducible RNAi constructs. The resulting constructs were introduced into Agrobacterium tumefaciens strain AGL1 by electroporation.
Transformation of M. truncatula
Transformation of M. truncatula 2HA leaf explants was carried out as described by Wang et al. (1996). The leaf explant preparation procedure was as described by Nolan et al. (2003). The 2HA sterilised explants were dipped into the Agrobacterium suspension and co-cultured on agar medium and incubated in the dark at 26°C for 2–3 days. The explants were washed with sterilised water and 500 μg ml−1 timentin before placing on P4 10:4 solid medium plus 500 μg ml−1 augmentin and 15 μg ml−1 hygromycin and incubated in the dark at 27°C. Hygromycin was used for transformed callus selection. The explants were subcultured every 4 weeks until somatic embryo development. For the RNAi studies transformed callus was used and RNAi constructs were induced by 2.5 μM dexamethasone.
For the MtWOX5 promoter::GUS studies transformation was carried out as above, but with auxin alone as the plant hormone to produce transformed roots.
The Medicagotruncatula WUS and WOX5 orthologs
In the case of MtWOX5 there was an expression pattern consistent with what is known of AtWOX5 expression (Fig. 3b). AtWOX5 is expressed in the quiescent centre of the root meristem (Sarkar et al. 2007) and in the developing embryo (Haecker et al. 2004). MtW0X5 was expressed in cultured roots and in the somatic embryo (Fig. 3b) and in the embryogenesis stage of M. truncatula pods (Supplementary Figure 1). There was little if any expression of MtW0X5 in the shoot apex, developing flower or leaf (Fig. 3b). Previous work on MtWOX5 by Imin et al. (2007) in M. truncatula showed that the apical part of the plant root has 57 times higher MtWOX5 expression compared to the elongation zone. In-situ hybridisation of seedling root tips (Fig. 4e) showed expression of MtWOX5 in the region of the quiescent centre. The signal was however consistently weaker than that of the MtWUS signals (Fig. 4a–d).
The sequence and expression data are consistent with the MtWUS and MtWOX5 being indeed functional orthologs of AtWUS and AtWOX5. The promoter::GUS studies supported the qRT-PCR studies.
Expression dynamics of MtWUS and MtWOX5 in relation to the induction of somatic embryogenesis and roots in culture
Although it was known that MtWOX5 is expressed in auxin-induced root formation in vitro (Imin et al. 2007), it remained important to understand its time course of expression to ascertain its relationship to root induction from procambial cells that we had previously described (Rose et al. 2006). MtWOX5 expression was induced by 2 days and was clearly auxin dependent (Fig. 5b). Maximum MtWOX5 expression occurred much later when roots were visible to the unaided eye.
MtWUS expression and the MtCLV3 relationship
MtWOX 5 expression and root meristem induction
WUSCHEL and somatic embryogenesis induction
The putative M. truncatulaWUS gene ortholog was obtained using the genome sequence and isolating the cDNA. Altogether eleven WOX genes from M. truncatula were identified and five of them ascribed to particular orthologs in Arabidopsis based on protein homology; MtWOX1, MtWOX3, MtWOX4, MtWOX5 and MtWOX9.
To obtain supporting evidence that the putative MtWUS was an ortholog of AtWUS, the expression pattern of MtWUS was initially examined in the intact plant prior to studying the expression in callus formation and SE. In the intact plant, MtWUS was expressed in the shoot apex (meristem and leaf primordium), in buds, and zygotic embryos but it was not expressed in leaves or roots. The expression pattern was similar to AtWUS in the shoot meristem and the flower primordium (Bäurle and Laux 2005; Müller et al. 2006). With in-situ hybridisations gene expression was present in the same positions in the shoot apex and heart-stage embryo as in Arabidopsis (Mayer et al. 1998). It seems clear that MtWUS is the AtWUS functional ortholog.
The WUS studies presented here support the predictions from the WUS overexpression studies by Zuo et al. (2002), namely that WUS expression is an essential for SE. In the M. truncatula SE system MtWUS expression is induced in the presence of auxin and cytokinin and also cytokinin alone, but not by auxin alone. This is consistent with what is known for the WUS and cytokinin relationships in the regulation of WUS in the Arabidopsis meristem (Leibfried et al. 2005). Further, Gordon et al. (2007) have shown cytokinin-induced AtWUS expression in shoot induction in in vitro cultures. The cytokinin-induced WUS expression in M. truncatula is in itself not enough to produce SEs as wild type Jemalong, which does not produce SEs, also showed cytokinin-stimulated WUS expression.
What is surprising is the rapid onset of MtWUS expression visualised as GUS staining across the whole leaf explant. Recently however, whole explant studies in our laboratory with explants cleared and stained with fuchsin have clearly revealed cell proliferation all over the explant, emanating from near the leaf veins.
During callus formation, groups of small cells with MtWUS expression are scattered around the callus. These clusters of cells are likely the source of cells that form embryos; MtWUS expression is clearly linked to these processes. However, as the embryogenic callus develops, MtWUS expression is confined to the somatic embryos themselves. These results indicate that MtWUS expresses in both undifferentiated cells in the callus and in the somatic embryo. This pattern is similar to AtWUS which is expressed in callus induced by cytokinin, and the expression increasingly localises in the differentiating shoot (Gordon et al. 2007). Our RNAi data also support a MtWUS requirement for callus formation and somatic embryo induction, which suggests that it also has a function to maintain undifferentiated stem cells like AtWUS. WUS, which has been suggested to be an embryo organiser (Zuo et al. 2002), appears to be associated with the production of totipotent stem cells, similar to the way it is involved in stem cell formation and maintenance in planta.
In the globular stage somatic embryo, MtWUS expression occurred throughout the whole embryo, which is not found in Arabidopsis zygotic embryos (Mayer et al. 1998). However, there are two points to note here: the hormonal environment is quite different in the somatic embryo developing in embryogenic callus, and the M. truncatula embryo is not likely to be identical to Arabidopsis in its developmental strategy. As the somatic embryo develops, MtWUS tends to localise towards the shoot pole.
The gene we have designated MtCLV3 is similar to AtCLV3 in peptide structure, genomic environment, and expression pattern. MtCLV3 also expresses in the shoot apex but not in flowers or leaves. It does not express in callus but is expressed in the shoot regions of later stage somatic embryos. MtWUS is initially expressed at high levels early in culture, unrestricted by CLV3 feedback, and as CLV3 is expressed it reduces WUS expression till eventually the well-known CLV3-WUS feedback loop characteristic of Arabidopsis shoot meristems is set up, i.e CLV3 down-regulates high WUS expression. Wild type Jemalong, which does not produce SEs, does not show CLV3 expression in culture.
WUS was induced in 24–48 h but the question remains as to how this expression relates to the overall process of SE induction. Previous work had shown that MtSERK1 was expressed 48 h after the beginning of culture, just after MtWUS expression, and it was associated with developmental change, thus marking cells as they change into a new developmental pathway (Nolan et al. 2003, 2009). MtSERF1 expression is evident after about 10 days of culture and is dependent on ethylene as well as auxin and cytokinin. It appears to act as a nexus between the stress of excision and culture (the stress reflected in ethylene synthesis) and the developmental hormones auxin and cytokinin driving cells into SE (Mantiri et al. 2008a, b). Importantly there is some evidence that cytokinin-induced WUS may be necessary for MtSERF1 expression as binding sites for the WUS transcription factor exist in the MtSERF1 promoter region (Mantiri et al. 2008a). It appears that MtSERF1, possibly in conjunction with WUS, is involved in regulating downstream genes required for SE (Mantiri et al. 2008a, b). MtSERF1 expression commences earlier than MtCLV3expression. MtCLV3 likely expresses when stem cells start to be regulated. RNAi studies with MtCLV3 would help resolve this question.
MtWOX5 expression in relation to de novo root formation
MtWOX5, based on the bioinformatics analysis is the putative ortholog of AtWOX5. The expression and in situ data presented here are consistent with this and confirm other recent work on MtWOX5 (Imin et al. 2007).
In-situ hybridisation of the roots induced in culture has suggested that MtWOX5 is expressed in the procambium cells and is associated with the induction of root primordia. It has been shown previously in our laboratory that root primordia were derived from these cells (Rose et al. 2006). In this it appears to have a somewhat similar role to WUS involvement in SE stem cell formation. After the root primordia formed, the meristem showed strong MtWOX5 expression, in what is the quiescent centre/stem cell area that is the source of the root cells and root cap cells. MtWOX5 expression was clearly auxin-dependent, contrasting with MtWUS. The GUS expression studies were not entirely consistent with the hybridisation studies as there are two areas of expression adjacent to the quiescent centre (Fig. 14a) as opposed to the more uniform hybridisation signals in the root tip (Fig. 13c, e). It is also possible that the promoter length, based on the sequence information we had for this study, was insufficient. Also there is the presence of the exogenous auxin associated with an in vitro system. Nevertheless the strong WOX5 expression in the primordium and meristem is clear.
In the intact Medicago plant, Imin et al. (2007) showed that there is low MtWOX5 expression in the root tip compared to root forming calli. This difference is apparent from the in situ studies presented here and suggests a strong auxin response in vitro, and expression outside the quiescent centre associated with the induction and development of the cultured roots. Auxin clearly up-regulates MtWOX5 expression (Fig. 5b) and we have observed in MtWOX5::GUS expressing meristems that increased auxin concentration increases the area of GUS expression. The Arabidopsis root has a closed meristem (Dolan et al. 1993), while M. truncatula being a legume has an open meristem (Heimsch and Seago 2008). Our study also indicated that there was MtWOX5 expression in the pericycle and procambial tissue of mature roots. It is feasible that this expression was related to a capacity for lateral root formation in planta. Such expression was not reported for Arabidopsis WOX5. The low expression of MtWOX5 in the root tip in planta relative to the in vitro expression was different to BBM (BABY BOOM) and PLT1 (PLETHORA 1) which expressed strongly in M. truncatula root-forming calli and root tips in planta (Imin et al. 2007).
MtWOX5 expression is very closely associated with root meristem formation and expresses in the stem cell areas of both the emerging primordium and in the cultured roots (Figs. 13, 14). The expression in the intact root meristem is likely confined to the quiescent centre as in Arabidopsis (Blilou et al. 2005). This may well be due to the close regulation by auxin which is different to the culture system (Gonzali et al. 2005). There is a parallel here with the MtWUS and SE induction as there is initial expression in many cells until the precision of the in planta regulation is set in train. However in vivo and in vitro WOX5 appears to act as a stem cell signal and is intimately associated with stem cell maintenance. RNAi studies would provide more direct evidence. MtWOX5 is also associated with embryo development and as shown recently, there is some overlap with WUS in their developmental roles (Sarkar et al. 2007).
Changes prior to WOX5 expression have not been well-documented, but ROS production could most likely be an initial event and the regulation of redox is an important consideration in setting up a root meristem (Imin et al. 2007). Other studies in M. truncatula also indicate induction of PLETHORA and BABY BOOM (Imin et al. 2007) known to be key players in stem cell maintenance in the Arabidopsis primary meristem (Galinha et al. 2007). However, we do not know the time course of their transcription in relation to WOX5.
Relationship between hormones and gene regulation in SE and root formation
It is apparent that the production of the SEs with their bipolar meristems and the production of the unipolar root meristem have different requirements for the key developmental and stress hormones. Through regulation of specific genes, hormones and morphogens are able to exert regulatory influence. In both cases the culture process has “hijacked” key developmental genes to drive the induction of the in vitro processes. Though these processes are not usual in the M. truncatula life cycle, similar processes do occur in nature. The relationship of ethylene to SE and in vitro root formation is different. In the case of SE ethylene is essential (Mantiri et al. 2008a, b) whereas for in vitro root formation it is inhibitory (Rose et al. 2006), suggesting a priority for reproduction.
MtWUS and MtWOX5 may have a similar function in relation to stem cell induction in vitro
MtWUS and MtWOX5 may have similar functions in stem cell initiation. WUS and WOX5 have been reported to have related roles in maintaining stem cells (Sarkar et al. 2007), and also have similar roles in stem cell induction in Medicago. WUS may induce stem cells for somatic embryos with cytokinin being essential, and WOX5, which is partially suppressed by cytokinin, may induce stem cells for root primordium formation with auxin being an essential co-regulator. The requirement for cytokinin and auxin in the regulation of the key genes is of course dependent on the species, genotype and explant type as well as the culture process.
This work was supported by an Australian Research Council Centre of Excellence grant (CEO348212) to the Australian Research Council Centre of Excellence for Integrative Legume Research.
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