AI Article Synopsis

  • Microsatellite markers are commonly used to measure genetic diversity in populations, but their effectiveness as proxies for broader genomic patterns was tested using 180 Arabidopsis halleri individuals and comparing them to genome-wide SNPs.
  • The study found that microsatellite diversity and estimates of genetic differentiation were significantly larger than those from SNPs, suggesting that microsatellites could have biases and do not always correlate with SNP diversity.
  • The researchers concluded that while some microsatellite markers may be useful, genome-wide SNP data offers more reliable estimates of genetic diversity and differentiation, with just a few thousand SNPs being sufficient for accurate assessments.

Article Abstract

Background: Microsatellite markers are widely used for estimating genetic diversity within and differentiation among populations. However, it has rarely been tested whether such estimates are useful proxies for genome-wide patterns of variation and differentiation. Here, we compared microsatellite variation with genome-wide single nucleotide polymorphisms (SNPs) to assess and quantify potential marker-specific biases and derive recommendations for future studies. Overall, we genotyped 180 Arabidopsis halleri individuals from nine populations using 20 microsatellite markers. Twelve of these markers were originally developed for Arabidopsis thaliana (cross-species markers) and eight for A. halleri (species-specific markers). We further characterized 2 million SNPs across the genome with a pooled whole-genome re-sequencing approach (Pool-Seq).

Results: Our analyses revealed that estimates of genetic diversity and differentiation derived from cross-species and species-specific microsatellites differed substantially and that expected microsatellite heterozygosity (SSR-H ) was not significantly correlated with genome-wide SNP diversity estimates (SNP-H and θ ) in A. halleri. Instead, microsatellite allelic richness (A ) was a better proxy for genome-wide SNP diversity. Estimates of genetic differentiation among populations (F ) based on both marker types were correlated, but microsatellite-based estimates were significantly larger than those from SNPs. Possible causes include the limited number of microsatellite markers used, marker ascertainment bias, as well as the high variance in microsatellite-derived estimates. In contrast, genome-wide SNP data provided unbiased estimates of genetic diversity independent of whether genome- or only exome-wide SNPs were used. Further, we inferred that a few thousand random SNPs are sufficient to reliably estimate genome-wide diversity and to distinguish among populations differing in genetic variation.

Conclusions: We recommend that future analyses of genetic diversity within and differentiation among populations use randomly selected high-throughput sequencing-based SNP data to draw conclusions on genome-wide diversity patterns. In species comparable to A. halleri, a few thousand SNPs are sufficient to achieve this goal.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225627PMC
http://dx.doi.org/10.1186/s12864-016-3459-7DOI Listing

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