Literature DB >> 3102974

The molecular clock runs more slowly in man than in apes and monkeys.

W H Li, M Tanimura.   

Abstract

The molecular clock hypothesis postulates that the rate of molecular evolution is approximately constant over time. Although this hypothesis has been highly controversial in the past, it is now widely accepted. The assumption of rate constancy has often been taken as a basis for reconstructing the phylogenetic relationships among organisms or genes and for dating evolutionary events. Further, it has been taken as strong support for the neutral mutation hypothesis, which postulates that the majority of molecular changes in evolution are due to neutral or nearly neutral mutations. For these reasons, the validity of the rate constancy assumption is a vital issue in molecular evolution. Recent studies using DNA sequence data have raised serious doubts about the hypothesis. These studies provided support for the suggestion made from immunological distance and protein sequence data that a rate slowdown has occurred in hominoid evolution, and showed, in agreement with DNA hybridization studies, that rates of nucleotide substitution are significantly higher in rodents than in man. Here, rates of nucleotide substitution in rodents are estimated to be 4-10 times higher than those in higher primates and 2-4 times higher than those in artiodactyls. Further, this study provides strong evidence for the hominoid slowdown hypothesis and suggests a further rate-slowdown in hominoid evolution. Our results suggest that the variation in rate among mammals is primarily due to differences in generation time rather than changes in DNA repair mechanisms. We also propose a method for estimating the divergence times between species when the rate constancy assumption is violated.

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Year:  1987        PMID: 3102974     DOI: 10.1038/326093a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  104 in total

1.  Estimating the age of the polydnavirus/braconid wasp symbiosis.

Authors:  James B Whitfield
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

2.  Purifying selection and birth-and-death evolution in the ubiquitin gene family.

Authors:  M Nei; I B Rogozin; H Piontkivska
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

3.  Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome.

Authors:  Ge Liu; Shaying Zhao; Jeffrey A Bailey; S Cenk Sahinalp; Can Alkan; Eray Tuzun; Eric D Green; Evan E Eichler
Journal:  Genome Res       Date:  2003-03       Impact factor: 9.043

4.  Neutral substitutions occur at a faster rate in exons than in noncoding DNA in primate genomes.

Authors:  Sankar Subramanian; Sudhir Kumar
Journal:  Genome Res       Date:  2003-05       Impact factor: 9.043

5.  Dating the monocot-dicot divergence and the origin of core eudicots using whole chloroplast genomes.

Authors:  Shu-Miaw Chaw; Chien-Chang Chang; Hsin-Liang Chen; Wen-Hsiung Li
Journal:  J Mol Evol       Date:  2004-04       Impact factor: 2.395

6.  Extensive variation in evolutionary rate of rbcL gene sequences among seed plants.

Authors:  J Bousquet; S H Strauss; A H Doerksen; R A Price
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

7.  The molecular clock ticks regularly in muroid rodents and hamsters.

Authors:  C O'hUigin; W H Li
Journal:  J Mol Evol       Date:  1992-11       Impact factor: 2.395

8.  Evidence for a convergent slowdown in primate molecular rates and its implications for the timing of early primate evolution.

Authors:  Michael E Steiper; Erik R Seiffert
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-02       Impact factor: 11.205

9.  Synonymous nucleotide substitution rates in mammalian genes: implications for the molecular clock and the relationship of mammalian orders.

Authors:  M Bulmer; K H Wolfe; P M Sharp
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

10.  Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era.

Authors:  J Jurka; E Zietkiewicz; D Labuda
Journal:  Nucleic Acids Res       Date:  1995-01-11       Impact factor: 16.971

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