Literature DB >> 21572094

Mutation rate distribution inferred from coincident SNPs and coincident substitutions.

Philip L F Johnson1, Ines Hellmann.   

Abstract

Mutation rate variation has the potential to bias evolutionary inference, particularly when rates become much higher than the mean. We first confirm prior work that inferred the existence of cryptic, site-specific rate variation on the basis of coincident polymorphisms-sites that are segregating in both humans and chimpanzees. Then we extend this observation to a longer evolutionary timescale by identifying sites of coincident substitutions using four species. From these data, we develop analytic theory to infer the variance and skewness of the distribution of mutation rates. Even excluding CpG dinucleotides, we find a relatively large coefficient of variation and positive skew, which suggests that, although most sites in the genome have mutation rates near the mean, the distribution contains a long right-hand tail with a small number of sites having high mutation rates. At least for primates, these quickly mutating sites are few enough that the infinite sites model in population genetics remains appropriate.

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Year:  2011        PMID: 21572094      PMCID: PMC3172574          DOI: 10.1093/gbe/evr044

Source DB:  PubMed          Journal:  Genome Biol Evol        ISSN: 1759-6653            Impact factor:   3.416


  23 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2010-01-04       Impact factor: 11.205

2.  Among-site rate variation and its impact on phylogenetic analyses.

Authors:  Z Yang
Journal:  Trends Ecol Evol       Date:  1996-09       Impact factor: 17.712

3.  Neutral behavior of shared polymorphism.

Authors:  A G Clark
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Authors:  Johannes Krause; Adrian W Briggs; Tomislav Maricic; Udo Stenzel; Martin Kircher; Nick Patterson; Richard E Green; Heng Li; Weiwei Zhai; Markus Hsi-Yang Fritz; Nancy F Hansen; Eric Y Durand; Anna-Sapfo Malaspinas; Jeffrey D Jensen; Tomas Marques-Bonet; Can Alkan; Kay Prüfer; Matthias Meyer; Hernán A Burbano; Jeffrey M Good; Rigo Schultz; Ayinuer Aximu-Petri; Anne Butthof; Barbara Höber; Barbara Höffner; Madlen Siegemund; Antje Weihmann; Chad Nusbaum; Eric S Lander; Carsten Russ; Nathaniel Novod; Jason Affourtit; Michael Egholm; Christine Verna; Pavao Rudan; Dejana Brajkovic; Željko Kucan; Ivan Gušic; Vladimir B Doronichev; Liubov V Golovanova; Carles Lalueza-Fox; Marco de la Rasilla; Javier Fortea; Antonio Rosas; Ralf W Schmitz; Philip L F Johnson; Evan E Eichler; Daniel Falush; Ewan Birney; James C Mullikin; Montgomery Slatkin; Rasmus Nielsen; Janet Kelso; Michael Lachmann; David Reich; Svante Pääbo
Journal:  Science       Date:  2010-05-07       Impact factor: 47.728

5.  The genomic distribution and local context of coincident SNPs in human and chimpanzee.

Authors:  Alan Hodgkinson; Adam Eyre-Walker
Journal:  Genome Biol Evol       Date:  2010-07-08       Impact factor: 3.416

6.  Estimation of hominoid ancestral population sizes under bayesian coalescent models incorporating mutation rate variation and sequencing errors.

Authors:  Ralph Burgess; Ziheng Yang
Journal:  Mol Biol Evol       Date:  2008-07-04       Impact factor: 16.240

7.  Genomic relationships and speciation times of human, chimpanzee, and gorilla inferred from a coalescent hidden Markov model.

Authors:  Asger Hobolth; Ole F Christensen; Thomas Mailund; Mikkel H Schierup
Journal:  PLoS Genet       Date:  2006-11-30       Impact factor: 5.917

8.  The diploid genome sequence of an individual human.

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Journal:  PLoS Biol       Date:  2007-09-04       Impact factor: 8.029

9.  Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data.

Authors:  Ryan N Gutenkunst; Ryan D Hernandez; Scott H Williamson; Carlos D Bustamante
Journal:  PLoS Genet       Date:  2009-10-23       Impact factor: 5.917

10.  Cryptic variation in the human mutation rate.

Authors:  Alan Hodgkinson; Emmanuel Ladoukakis; Adam Eyre-Walker
Journal:  PLoS Biol       Date:  2009-02-03       Impact factor: 8.029

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  12 in total

Review 1.  Variation in the mutation rate across mammalian genomes.

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2.  On the prospect of achieving accurate joint estimation of selection with population history.

Authors:  Parul Johri; Adam Eyre-Walker; Ryan N Gutenkunst; Kirk E Lohmueller; Jeffrey D Jensen
Journal:  Genome Biol Evol       Date:  2022-07-02       Impact factor: 4.065

Review 3.  The origin of human mutation in light of genomic data.

Authors:  Vladimir B Seplyarskiy; Shamil Sunyaev
Journal:  Nat Rev Genet       Date:  2021-06-23       Impact factor: 53.242

4.  Interaction-based evolution: how natural selection and nonrandom mutation work together.

Authors:  Adi Livnat
Journal:  Biol Direct       Date:  2013-10-18       Impact factor: 4.540

5.  Mutation Rate Variation is a Primary Determinant of the Distribution of Allele Frequencies in Humans.

Authors:  Arbel Harpak; Anand Bhaskar; Jonathan K Pritchard
Journal:  PLoS Genet       Date:  2016-12-15       Impact factor: 5.917

6.  Prevalence of multinucleotide replacements in evolution of primates and Drosophila.

Authors:  Nadezhda V Terekhanova; Georgii A Bazykin; Alexey Neverov; Alexey S Kondrashov; Vladimir B Seplyarskiy
Journal:  Mol Biol Evol       Date:  2013-02-27       Impact factor: 16.240

7.  How much of the variation in the mutation rate along the human genome can be explained?

Authors:  Adam Eyre-Walker; Ying Chen Eyre-Walker
Journal:  G3 (Bethesda)       Date:  2014-07-03       Impact factor: 3.154

8.  Purifying selection shapes the coincident SNP distribution of primate coding sequences.

Authors:  Chia-Ying Chen; Li-Yuan Hung; Chan-Shuo Wu; Trees-Juen Chuang
Journal:  Sci Rep       Date:  2016-06-03       Impact factor: 4.379

9.  Are sites with multiple single nucleotide variants in cancer genomes a consequence of drivers, hypermutable sites or sequencing errors?

Authors:  Thomas C A Smith; Antony M Carr; Adam C Eyre-Walker
Journal:  PeerJ       Date:  2016-09-20       Impact factor: 2.984

10.  APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context.

Authors:  Vladimir B Seplyarskiy; Maria A Andrianova; Georgii A Bazykin
Journal:  Genome Res       Date:  2016-12-09       Impact factor: 9.043

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