Abstract
TOPO6, a nuclear gene-marker region of subunit B of the plant homolog of archaean topoisomerase VI, occurs as single-copy locus in the haploid genome of most plant groups. The gene consists mainly of 19 exons and 18 introns, which provide conserved primer binding sites for PCR amplification in many angiosperm families combined with variable sequence stretches that can be explored in molecular systematics. Here intron/exon structure, sequence diversity, and a set of amplification primers are described to use TOPO6 as single-copy phylogenetic marker region in a wide range of plant taxa, either through PCR amplification or hybridization-based sequence capture.
References
Álvarez I, Wendel JF (2003) Ribosomal ITS sequences and plant phylogenetic inference. Molec Phylogen Evol 29:417–434
Bates AD, Maxwell A (2005) DNA topology. Oxford Univ Press, Oxford
Blaner A, Schneider J, Röser M (2014) Phylogenetic relationships in the grass family (Poaceae) based on the nuclear single copy locus topoisomerase 6 compared with chloroplast DNA. Syst Biodivers 12:111–124
Blattner FR (1999) Direct amplification of the entire ITS region from poorly preserved plant material using recombinant PCR. Biotechniques 29:1180–1186
Brassac J, Blattner FR (2015) Species-level phylogeny and polyploid relationships in Hordeum (Poaceae) inferred by next-generation sequencing and in silico cloning of multiple nuclear loci. Syst Biol 64:792–808
Brassac J, Jakob SS, Blattner FR (2012) Progenitor–derivative relationships of Hordeum polyploids (Poaceae, Triticeae) inferred from sequences of TOPO6, a nuclear low-copy gene region. PLoS ONE 7:e33808
Chamala S, García N, Godden GT, Krishnakumar V, Jordon-Thaden IE, de Smet R, Barbazuk WB, Soltis DE, Soltis PS (2015) MarkerMiner 1.0: a new application for phylogenetic marker development using angiosperm transcriptomes. Appl Pl Sci 3:1400115
de Smet R, Adams KL, Vandepoele K, Van Montagu MCE, Maere S, Van de Peer Y (2013) Convergent gene loss following gene and genome duplications creates single-copy families in flowering plants. Proc Natl Acad Sci USA 110:2898–2903
Hartung F, Blattner FR, Puchta H (2002) Intron gain and loss in the evolution of the conserved eukaryotic recombination machinery. Nucleic Acids Res 30:5175–5181
Hochbach A, Schneider J, Röser M (2015) A multi-locus analysis of phylogenetic relationships within grass subfamily Pooideae (Poaceae) inferred from sequences of nuclear single copy gene regions compared with plastid DNA. Molec Phylogen Evol 87:14–27
Jakob SS, Blattner FR (2010) Two extinct diploid progenitors involved in allopolyploid formation in the Hordeum murinum (Poaceae: Triticeae) taxon complex. Molec Phylogen Evol 55:650–659
Jakob SS, Heibl C, Rödder D, Blattner FR (2010) Population demography influences climatic niche evolution: evidence from diploid American Hordeum species (Poaceae). Molec Ecol 19:1423–1438
Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD, Gibson TJ, Higgins DG (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–2948
Lemmon EM, Lemmon AR (2013) High-throughput genomic data in systematics and phylogenetics. Annu Rev Ecol Evol Syst 44:99–121
Maddison WP (1997) Gene trees in species trees. Syst Biol 46:523–536
Mamanova L, Coffey AJ, Scott CE, Kozarewa I, Turner EH, Kumar A, Howard E, Shendure J, Turner DJ (2009) Target-enrichment strategies for next-generation sequencing. Nature Meth 7:111–118
McCormack JE, Hird SM, Zellmer AJ, Carstens BC, Brumfield RT (2013) Application of next-generation sequencing to phylogeography and phylogenetics. Molec Phylogen Evol 66:526–538
Naciri Y, Linder HP (2015) Species delimitation and relationships: the dance of the seven veils. Taxon 64:3–17
Nickrent DL, Soltis DE (1995) A comparison of angiosperm phylogenies from nuclear 18S rDNA and rbcL sequences. Ann Missouri Bot Gard 82:208–234
Proost S, Van Bel M, Vaneechoutte D, Van de Peer Y, Inzé D, Mueller-Roeber B, Vanderpoele K (2014) PLAZA 3.0: an access point for plant comparative genomics. Nucleic Acids Res 43:D974–D981
Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP (2012) MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol 61:539–542
Swofford DL (2002) PAUP*. Phylogenetic analysis using parsimony (*and other methods), version 4. Sinauer Associates, Sunderland
Weitemier K, Straub SCK, Cronn RC, Fishbein M, Schmickl R, McDonnell A, Liston A (2014) Hyb-Seq: combining target enrichment and genome skimming for plant phylogenomics. Appl Pl Sci 2:1400042
White TJ, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ (eds) PCR protocols: a guide to methods and applications. Academic Press, San Diego, pp 315–322
Wölk A, Röser M (2014) Polyploid evolution, intercontinental biogeographical relationships and morphology of the recently described African oat genus Trisetopsis (Poaceae). Taxon 63:773–788
Wölk A, Winterfeld G, Röser M (2015) Genome evolution in a Mediterranean species complex: phylogeny and cytogenetics of Helictotrichon (Poaceae) allopolyploids based on nuclear DNA sequences (rDNA, topoisomerase gene) and FISH. Syst Biodivers 13:326–345
Zimmer EA, Wen J (2012) Using nuclear gene data for plant phylogenetics: progress and prospects. Molec Phylogen Evol 65:774–785
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The author declares that he has no conflict of interest.
Funding
Parts of this study were funded by the German Research Foundation (DFG) through Grant JA1938/2.
Additional information
Handling editor: Marcus Koch.
Electronic supplementary material
Below is the link to the electronic supplementary material.
606_2015_1259_MOESM1_ESM.txt
Supplementary material 1 Alignment of the topoisomerase VI B coding regions of 36 plant taxa (FASTA format) used to infer sequence homology and positions of potentially conserved priming sites for amplification of TOPO6 parts by PCR. The genomic sequence of A. thaliana was included to indicate positions of introns and exons. The alignment can be explored with any sequence-alignment or editor program. Primer positions (Table 1) are indicated by stretches of ‘N’ in the first line (TXT 163 kb)
606_2015_1259_MOESM2_ESM.txt
Supplementary material 2 Alignment of coding and genomic sequences of Oryza sativa, Arabidopsis thaliana, Vitis vinifera, Ricinus communis, and Malus domestica (FASTA format) used to provide information on the range of intron length variation in angiosperm taxa (TXT 107 kb)
606_2015_1259_MOESM3_ESM.pdf
Supplementary material 3 Neighbor-joining tree of 96 topoisomerase VI B sequences obtained from GeneBank to infer the occurrence of deep paralogs (PDF 4682 kb)
606_2015_1259_MOESM4_ESM.pdf
Supplementary material 4 Bayesian phylogenetic tree derived from coding regions of topoisomerase VI B sequences of diverse land plants (PDF 367 kb)
Rights and permissions
About this article
Cite this article
Blattner, F.R. TOPO6: a nuclear single-copy gene for plant phylogenetic inference. Plant Syst Evol 302, 239–244 (2016). https://doi.org/10.1007/s00606-015-1259-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00606-015-1259-1