Literature DB >> 22174068

The coalescent with selection on copy number variants.

Kosuke M Teshima1, Hideki Innan.   

Abstract

We develop a coalescent-based simulation tool to generate patterns of single nucleotide polymorphisms (SNPs) in a wide region encompassing both the original and duplicated genes. Selection on the new duplicated copy and interlocus gene conversion between the two copies are incorporated. This simulation enables us to explore how selection on duplicated copies affects the pattern of SNPs. The fixation of an advantageous duplicated copy causes a strong reduction in polymorphism not only in the duplicated copy but also in its flanking regions, which is a typical signature of a selective sweep by positive selection. After fixation, polymorphism gradually increases by accumulating neutral mutations and eventually reaches the equilibrium value if there is no gene conversion. When gene conversion is active, the number of SNPs in the duplicated copy quickly increases by transferring SNPs from the original copy; therefore, the time when we can recognize the signature of selection is decreased. Because this effect of gene conversion is restricted only to the duplicated region, more power to detect selection is expected if a flanking region to the duplicated copy is used.

Mesh:

Year:  2011        PMID: 22174068      PMCID: PMC3296243          DOI: 10.1534/genetics.111.135343

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  51 in total

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4.  Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.

Authors:  F Tajima
Journal:  Genetics       Date:  1989-11       Impact factor: 4.562

5.  Statistical tests of neutrality of mutations.

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Journal:  Genetics       Date:  1993-03       Impact factor: 4.562

Review 6.  Chromosomal duplications in bacteria, fruit flies, and humans.

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Review 7.  Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits.

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10.  The coalescent process in models with selection and recombination.

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Journal:  Genetics       Date:  1988-11       Impact factor: 4.562

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  11 in total

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7.  Copy number variation contributes to cryptic genetic variation in outbreak lineages of Cryptococcus gattii from the North American Pacific Northwest.

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8.  Intraspecific evolution of human RCCX copy number variation traced by haplotypes of the CYP21A2 gene.

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9.  Effect of Collapsed Duplications on Diversity Estimates: What to Expect.

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10.  Population Genetics of the Highly Polymorphic RPP8 Gene Family.

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