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Published on: November 15, 2017
A weak effect of background selection on trinucleotide microsatellites in maize
Anne-Céline Thuillet1, Maud I Tenaillon, Lorinda K Anderson
1Department of Genetics, University of Wisconsin, Madison, WI 53706, USA.
Artificial selection in maize domestication did not significantly impact neutral diversity genome-wide. However, a weak correlation between recombination and microsatellite diversity suggests background selection influenced specific gene regions.
Area of Science:
- Genetics
- Evolutionary Biology
- Genomics
Background:
- Artificial selection during maize domestication is believed to primarily involve positive selection, with minimal impact on neutral genetic diversity due to rapid linkage disequilibrium breakdown.
- The extent to which indirect selection has shaped neutral diversity across the maize genome during domestication is not fully understood.
Purpose of the Study:
- To investigate the relationship between local recombination rates and neutral polymorphism in maize and its wild ancestor, teosinte.
- To quantify genetic diversity using parameters sensitive to indirect selection and mutation.
Main Methods:
- Utilized both DNA sequence and microsatellite data from maize and teosinte.
- Estimated three key parameters to measure genetic diversity and infer the effects of selection and mutation.
Main Results:
- Found no consistent genome-wide correlation between genetic diversity and recombination rates in maize.
- Observed a weak positive correlation between heterozygosity and recombination for specific microsatellites within genes, deviating from the stepwise mutation model.
- This correlation was not observed for nucleotide diversity, suggesting stronger purifying selection near these microsatellites.
Conclusions:
- Indirect selection appears to have had a limited genome-wide effect on neutral diversity in maize.
- Background selection may play a role in shaping diversity at specific microsatellite loci within genes.
- Purifying selection might be more potent at certain microsatellite regions compared to nucleotide mutations.
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