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De novo transcriptome assembly of Pueraria montana var. lobata and Neustanthus phaseoloides for the development of eSSR and SNP markers: narrowing the US origin(s) of the invasive kudzu

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dc.contributor.author Haynsen, Matthew S. en
dc.contributor.author Vatanparast, Mohammad en
dc.contributor.author Mahadwar, Gouri en
dc.contributor.author Zhu, Dennis en
dc.contributor.author Moger-Reischer, Roy en
dc.contributor.author Doyle, Jeff J. en
dc.contributor.author Crandall, Keith A. en
dc.contributor.author Egan, Ashley N. en
dc.date.accessioned 2018-06-22T09:01:16Z
dc.date.available 2018-06-22T09:01:16Z
dc.date.issued 2018
dc.identifier.citation Haynsen, Matthew S., Vatanparast, Mohammad, Mahadwar, Gouri, Zhu, Dennis, Moger-Reischer, Roy, Doyle, Jeff J., Crandall, Keith A., and Egan, Ashley N. 2018. "De novo transcriptome assembly of Pueraria montana var. lobata and Neustanthus phaseoloides for the development of eSSR and SNP markers: narrowing the US origin(s) of the invasive kudzu." <em>BMC genomics</em>. 19 (1):439. <a href="https://doi.org/10.1186/s12864-018-4798-3">https://doi.org/10.1186/s12864-018-4798-3</a> en
dc.identifier.issn 1471-2164
dc.identifier.uri https://hdl.handle.net/10088/35789
dc.description.abstract BACKGROUND: Kudzu, Pueraria montana var. lobata, is a woody vine native to Southeast Asia that has been introduced globally for cattle forage and erosion control. The vine is highly invasive in its introduced areas, including the southeastern US. Modern molecular marker resources are limited for the species, despite its importance. Transcriptomes for P. montana var. lobata and a second phaseoloid legume taxon previously ascribed to genus Pueraria, Neustanthus phaseoloides, were generated and mined for microsatellites and single nucleotide polymorphisms. RESULTS: Roche 454 sequencing of P. montana var. lobata and N. phaseoloides transcriptomes produced read numbers ranging from ~ 280,000 to ~ 420,000. Trinity assemblies produced an average of 17,491 contigs with mean lengths ranging from 639 bp to 994 bp. Transcriptome completeness, according to BUSCO, ranged between 64 and 77%. After vetting for primer design, there were 1646 expressed simple sequence repeats (eSSRs) identified in P. montana var. lobata and 1459 in N. phaseoloides. From these eSSRs, 17 identical primer pairs, representing inter-generic phaseoloid eSSRs, were created. Additionally, 13 primer pairs specific to P. montana var. lobata were also created. From these 30 primer pairs, a final set of seven primer pairs were used on 68 individuals of P. montana var. lobata for characterization across the US, China, and Japan. The populations exhibited from 20 to 43 alleles across the seven loci. We also conducted pairwise tests for high-confidence SNP discovery from the kudzu transcriptomes we sequenced and two previously sequenced P. montana var. lobata transcriptomes. Pairwise comparisons between P. montana var. lobata ranged from 358 to 24,475 SNPs, while comparisons between P. montana var. lobata and N. phaseoloides ranged from 5185 to 30,143 SNPs. CONCLUSIONS: The discovered molecular markers for kudzu provide a starting point for comparative genetic studies within phaseoloid legumes. This study both adds to the current genetic resources and presents the first available genomic resources for the invasive kudzu vine. Additionally, this study is the first to provide molecular evidence to support the hypothesis of Japan as a source of US kudzu and begins to narrow the origin of US kudzu to the central Japanese island of Honshu. en
dc.relation.ispartof BMC genomics en
dc.title De novo transcriptome assembly of Pueraria montana var. lobata and Neustanthus phaseoloides for the development of eSSR and SNP markers: narrowing the US origin(s) of the invasive kudzu en
dc.type Journal Article en
dc.identifier.srbnumber 146698
dc.identifier.doi 10.1186/s12864-018-4798-3
rft.jtitle BMC genomics
rft.volume 19
rft.issue 1
rft.spage 439
dc.description.SIUnit NH-Botany en
dc.description.SIUnit NH-Invertebrate Zoology en
dc.description.SIUnit NMNH en
dc.description.SIUnit Peer-reviewed en
dc.citation.spage 439


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