Cargando…
Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations
BACKGROUND: DNA barcoding of land plants has relied traditionally on a small number of markers from the plastid genome. In contrast, low-copy nuclear genes have received little attention as DNA barcodes because of the absence of universal primers for PCR amplification. RESULTS: From pooled-species 4...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605094/ https://www.ncbi.nlm.nih.gov/pubmed/23394592 http://dx.doi.org/10.1186/1471-2148-13-35 |
_version_ | 1782263818287579136 |
---|---|
author | Pillon, Yohan Johansen, Jennifer Sakishima, Tomoko Chamala, Srikar Barbazuk, W Brad Roalson, Eric H Price, Donald K Stacy, Elizabeth A |
author_facet | Pillon, Yohan Johansen, Jennifer Sakishima, Tomoko Chamala, Srikar Barbazuk, W Brad Roalson, Eric H Price, Donald K Stacy, Elizabeth A |
author_sort | Pillon, Yohan |
collection | PubMed |
description | BACKGROUND: DNA barcoding of land plants has relied traditionally on a small number of markers from the plastid genome. In contrast, low-copy nuclear genes have received little attention as DNA barcodes because of the absence of universal primers for PCR amplification. RESULTS: From pooled-species 454 transcriptome data we identified two variable intron-less nuclear loci for each of two species-rich genera of the Hawaiian flora: Clermontia (Campanulaceae) and Cyrtandra (Gesneriaceae) and compared their utility as DNA barcodes with that of plastid genes. We found that nuclear genes showed an overall greater variability, but also displayed a high level of heterozygosity, intraspecific variation, and retention of ancient alleles. Thus, nuclear genes displayed fewer species-diagnostic haplotypes compared to plastid genes and no interspecies gaps. CONCLUSIONS: The apparently greater coalescence times of nuclear genes are likely to limit their utility as barcodes, as only a small proportion of their alleles were fixed and unique to individual species. In both groups, species-diagnostic markers from either genome were scarce on the youngest island; a minimum age of ca. two million years may be needed for a species flock to be barcoded. For young plant groups, nuclear genes may not be a superior alternative to slowly evolving plastid genes. |
format | Online Article Text |
id | pubmed-3605094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36050942013-03-22 Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations Pillon, Yohan Johansen, Jennifer Sakishima, Tomoko Chamala, Srikar Barbazuk, W Brad Roalson, Eric H Price, Donald K Stacy, Elizabeth A BMC Evol Biol Research Article BACKGROUND: DNA barcoding of land plants has relied traditionally on a small number of markers from the plastid genome. In contrast, low-copy nuclear genes have received little attention as DNA barcodes because of the absence of universal primers for PCR amplification. RESULTS: From pooled-species 454 transcriptome data we identified two variable intron-less nuclear loci for each of two species-rich genera of the Hawaiian flora: Clermontia (Campanulaceae) and Cyrtandra (Gesneriaceae) and compared their utility as DNA barcodes with that of plastid genes. We found that nuclear genes showed an overall greater variability, but also displayed a high level of heterozygosity, intraspecific variation, and retention of ancient alleles. Thus, nuclear genes displayed fewer species-diagnostic haplotypes compared to plastid genes and no interspecies gaps. CONCLUSIONS: The apparently greater coalescence times of nuclear genes are likely to limit their utility as barcodes, as only a small proportion of their alleles were fixed and unique to individual species. In both groups, species-diagnostic markers from either genome were scarce on the youngest island; a minimum age of ca. two million years may be needed for a species flock to be barcoded. For young plant groups, nuclear genes may not be a superior alternative to slowly evolving plastid genes. BioMed Central 2013-02-09 /pmc/articles/PMC3605094/ /pubmed/23394592 http://dx.doi.org/10.1186/1471-2148-13-35 Text en Copyright ©2013 Pillon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pillon, Yohan Johansen, Jennifer Sakishima, Tomoko Chamala, Srikar Barbazuk, W Brad Roalson, Eric H Price, Donald K Stacy, Elizabeth A Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title | Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title_full | Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title_fullStr | Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title_full_unstemmed | Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title_short | Potential use of low-copy nuclear genes in DNA barcoding: a comparison with plastid genes in two Hawaiian plant radiations |
title_sort | potential use of low-copy nuclear genes in dna barcoding: a comparison with plastid genes in two hawaiian plant radiations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605094/ https://www.ncbi.nlm.nih.gov/pubmed/23394592 http://dx.doi.org/10.1186/1471-2148-13-35 |
work_keys_str_mv | AT pillonyohan potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT johansenjennifer potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT sakishimatomoko potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT chamalasrikar potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT barbazukwbrad potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT roalsonerich potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT pricedonaldk potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations AT stacyelizabetha potentialuseoflowcopynucleargenesindnabarcodingacomparisonwithplastidgenesintwohawaiianplantradiations |