Development, validation and high-throughput analysis of sequence markers in nonmodel species
DNA sequences derived from multiple regions of the nuclear genome are essential for historical inferences in the fields of phylogeography and phylogenetics. The appropriate markers should be single‐copy, variable, easy to amplify from multiple samples and easy to sequence using high‐throughput techn...
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Published in | Molecular ecology resources Vol. 14; no. 2; pp. 352 - 360 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.03.2014
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | DNA sequences derived from multiple regions of the nuclear genome are essential for historical inferences in the fields of phylogeography and phylogenetics. The appropriate markers should be single‐copy, variable, easy to amplify from multiple samples and easy to sequence using high‐throughput technologies. This may be difficult to achieve for species lacking sequenced genomes and particularly challenging for species possessing large genomes, which consist mostly of repetitive sequences. Here, we present a cost‐effective, broadly applicable framework for designing, validating and high‐throughput sequencing of multiple markers in nonmodel species without sequenced genomes. We demonstrate its utility in two closely related species of newts, representatives of urodeles, a vertebrate group characterized by large genomes. We show that over 80 markers, c. 600 bp each, developed mainly from 3′ untranslated transcript regions (3′UTR) may be effectively multiplexed and sequenced. Data are further processed using standard, freely available bioinformatic tools, producing phase‐resolved sequences. The approach does not require barcoded PCR primers, and the cost of library preparation is independent of the number of markers investigated. We hope that this approach will be of broad interest for researchers working at the interface of population genetics and phylogenetics, exploring deep intraspecific genetic structure, species boundaries and phylogeographies of closely related species. |
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Bibliography: | Polish National Science Center - No. 8171/B/P01/2011/40; No. UMO-2012/04/A/NZ8/00662 istex:5E4D661791B8B34FFE477C71FE53AE9A9C2D2DE3 ArticleID:MEN12171 Jagiellonian University - No. DS/WBiNoZ/INoS/762/12 Fig. S1 The per-base average coverage for individuals averaged across markers. Means ± SD are presented.Table S1 Sampling locality and amplification method used for each individual. Table S2 Sequence markers developed from transcriptome of Lissotriton newts. Table S3 Average coverage depth per marker per individual. Table S4 Relative coverage per marker per individual expressed as a percentage of the total coverage (PTC) obtained for individual. Table S5 Basic statistics of DNA polymorphism in Lissotriton montandoni and L. vulgaris. ark:/67375/WNG-1Z787MZH-N ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1755-098X 1755-0998 |
DOI: | 10.1111/1755-0998.12171 |