Genomic patterns of introgression in rainbow and westslope cutthroat trout illuminated by overlapping paired-end RAD sequencing

被引:150
作者
Hohenlohe, Paul A. [1 ]
Day, Mitch D. [1 ]
Amish, Stephen J. [2 ]
Miller, Michael R. [3 ]
Kamps-Hughes, Nick [3 ]
Boyer, Matthew C. [4 ]
Muhlfeld, Clint C. [5 ,6 ]
Allendorf, Fred W. [2 ]
Johnson, Eric A. [3 ]
Luikart, Gordon [6 ]
机构
[1] Univ Idaho, Dept Biol Sci, Inst Bioinformat & Evolutionary Studies, Moscow, ID 83844 USA
[2] Univ Montana, Div Biol Sci, Fish & Wildlife Genom Grp, Missoula, MT 59812 USA
[3] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
[4] Montana Fish Wildlife & Pk, Kalispell, MT 59901 USA
[5] US Geol Survey, Northern Rocky Mt Sci Ctr, West Glacier, MT 59936 USA
[6] Univ Montana, Flathead Lake Biol Stn, Fish & Wildlife Genom Grp, Div Biol Sci, Polson, MT 59860 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
adaptive introgression; conservation genomics; hybridization; invasive species; natural selection; next-generation sequencing; salmonids; super invasive genes; SINGLE-NUCLEOTIDE POLYMORPHISMS; SNP DISCOVERY; ONCORHYNCHUS-MYKISS; POPULATION GENOMICS; HYBRIDIZATION; CONSERVATION; BINDING; SPREAD; IDENTIFICATION; MARKERS;
D O I
10.1111/mec.12239
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
Rapid and inexpensive methods for genomewide single nucleotide polymorphism (SNP) discovery and genotyping are urgently needed for population management and conservation. In hybridized populations, genomic techniques that can identify and genotype thousands of species-diagnostic markers would allow precise estimates of population- and individual-level admixture as well as identification of super invasive' alleles, which show elevated rates of introgression above the genomewide background (likely due to natural selection). Techniques like restriction-site-associated DNA (RAD) sequencing can discover and genotype large numbers of SNPs, but they have been limited by the length of continuous sequence data they produce with Illumina short-read sequencing. We present a novel approach, overlapping paired-end RAD sequencing, to generate RAD contigs of >300-400bp. These contigs provide sufficient flanking sequence for design of high-throughput SNP genotyping arrays and strict filtering to identify duplicate paralogous loci. We applied this approach in five populations of native westslope cutthroat trout that previously showed varying (low) levels of admixture from introduced rainbow trout (RBT). We produced 77141 RAD contigs and used these data to filter and genotype 3180 previously identified species-diagnostic SNP loci. Our population-level and individual-level estimates of admixture were generally consistent with previous microsatellite-based estimates from the same individuals. However, we observed slightly lower admixture estimates from genomewide markers, which might result from natural selection against certain genome regions, different genomic locations for microsatellites vs. RAD-derived SNPs and/or sampling error from the small number of microsatellite loci (n=7). We also identified candidate adaptive super invasive alleles from RBT that had excessively high admixture proportions in hybridized cutthroat trout populations.
引用
收藏
页码:3002 / 3013
页数:12
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