Literature DB >> 25931515

Relaxing the Molecular Clock to Different Degrees for Different Substitution Types.

Hui-Jie Lee1, Nicolas Rodrigue2, Jeffrey L Thorne3.   

Abstract

Rates of molecular evolution can vary over time. Diverse statistical techniques for divergence time estimation have been developed to accommodate this variation. These typically require that all sequence (or codon) positions at a locus change independently of one another. They also generally assume that the rates of different types of nucleotide substitutions vary across a phylogeny in the same way. This permits divergence time estimation procedures to employ an instantaneous rate matrix with relative rates that do not differ among branches. However, previous studies have suggested that some substitution types (e.g., CpG to TpG changes in mammals) are more clock-like than others. As has been previously noted, this is biologically plausible given the mutational mechanism of CpG to TpG changes. Through stochastic mapping of sequence histories from context-independent substitution models, our approach allows for context-dependent nucleotide substitutions to change their relative rates over time. We apply our approach to the analysis of a 0.15 Mb intergenic region from eight primates. In accord with previous findings, we find comparatively little rate variation over time for CpG to TpG substitutions but we find more for other substitution types. We conclude by discussing the limitations and prospects of our approach.
© The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Keywords:  CpG transition rate; context-dependent substitution; divergence time estimation; relaxed molecular clock

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Year:  2015        PMID: 25931515      PMCID: PMC4833082          DOI: 10.1093/molbev/msv099

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  43 in total

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6.  Is there an acceleration of the CpG transition rate during the mammalian radiation?

Authors:  M Peifer; J E Karro; H H von Grünberg
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8.  Estimation of primate speciation dates using local molecular clocks.

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Authors:  Augustine Kong; Michael L Frigge; Gisli Masson; Soren Besenbacher; Patrick Sulem; Gisli Magnusson; Sigurjon A Gudjonsson; Asgeir Sigurdsson; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Wendy S W Wong; Gunnar Sigurdsson; G Bragi Walters; Stacy Steinberg; Hannes Helgason; Gudmar Thorleifsson; Daniel F Gudbjartsson; Agnar Helgason; Olafur Th Magnusson; Unnur Thorsteinsdottir; Kari Stefansson
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  3 in total

1.  Grouping substitution types into different relaxed molecular clocks.

Authors:  Hui-Jie Lee; Hirohisa Kishino; Nicolas Rodrigue; Jeffrey L Thorne
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-07-19       Impact factor: 6.237

2.  Variation in the molecular clock of primates.

Authors:  Priya Moorjani; Carlos Eduardo G Amorim; Peter F Arndt; Molly Przeworski
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-06       Impact factor: 11.205

3.  Pedigree-based and phylogenetic methods support surprising patterns of mutation rate and spectrum in the gray mouse lemur.

Authors:  C Ryan Campbell; George P Tiley; Jelmer W Poelstra; Kelsie E Hunnicutt; Peter A Larsen; Hui-Jie Lee; Jeffrey L Thorne; Mario Dos Reis; Anne D Yoder
Journal:  Heredity (Edinb)       Date:  2021-07-16       Impact factor: 3.832

  3 in total

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