Unlocking the vault: next-generation museum population genomics

被引:291
作者
Bi, Ke [1 ]
Linderoth, Tyler [1 ,2 ]
Vanderpool, Dan [3 ]
Good, Jeffrey M. [3 ]
Nielsen, Rasmus [2 ]
Moritz, Craig [1 ,2 ,4 ,5 ]
机构
[1] Univ Calif Berkeley, Museum Vertebrate Zool, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[3] Univ Montana, Div Biol Sci, Missoula, MT 59812 USA
[4] Australian Natl Univ, Res Sch Biol, Canberra, ACT 0200, Australia
[5] Australian Natl Univ, Ctr Biodivers Anal, Canberra, ACT 0200, Australia
基金
加拿大自然科学与工程研究理事会;
关键词
DNA damage; exon capture; museum skins; natural history museum collections; nonmodel organisms; Tamias; HISTORICAL DNA ANALYSIS; MITOCHONDRIAL-DNA; GENETIC-VARIABILITY; SNP DISCOVERY; LOW-COST; CAPTURE; CLIMATE; DIVERSITY; SEQUENCES; HYBRIDIZATION;
D O I
10.1111/mec.12516
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural history museum collections provide unique resources for understanding how species respond to environmental change, including the abrupt, anthropogenic climate change of the past century. Ideally, researchers would conduct genome-scale screening of museum specimens to explore the evolutionary consequences of environmental changes, but to date such analyses have been severely limited by the numerous challenges of working with the highly degraded DNA typical of historic samples. Here, we circumvent these challenges by using custom, multiplexed, exon capture to enrich and sequence similar to 11000 exons (similar to 4Mb) from early 20th-century museum skins. We used this approach to test for changes in genomic diversity accompanying a climate-related range retraction in the alpine chipmunks (Tamias alpinus) in the high Sierra Nevada area of California, USA. We developed robust bioinformatic pipelines that rigorously detect and filter out base misincorporations in DNA derived from skins, most of which likely resulted from postmortem damage. Furthermore, to accommodate genotyping uncertainties associated with low-medium coverage data, we applied a recently developed probabilistic method to call single-nucleotide polymorphisms and estimate allele frequencies and the joint site frequency spectrum. Our results show increased genetic subdivision following range retraction, but no change in overall genetic diversity at either nonsynonymous or synonymous sites. This case study showcases the advantages of integrating emerging genomic and statistical tools in museum collection-based population genomic applications. Such technical advances greatly enhance the value of museum collections, even where a pre-existing reference is lacking and points to a broad range of potential applications in evolutionary and conservation biology.
引用
收藏
页码:6018 / 6032
页数:15
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