Genomic clocks and evolutionary timescales

被引:187
作者
Hedges, SB [1 ]
Kumar, S
机构
[1] Penn State Univ, NASA Astrobiol Inst, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biol, Mueller Lab 208, University Pk, PA 16802 USA
[3] Arizona State Univ, Ctr Evolut Funct Genom, Arizona Biodesign Inst, Tempe, AZ 85287 USA
[4] Arizona State Univ, Dept Biol, Tempe, AZ 85287 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/S0168-9525(03)00053-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For decades, molecular clocks have helped to illuminate the evolutionary timescale of life, but now genomic data pose a challenge for time estimation methods. It is unclear how to integrate data from many genes, each potentially evolving under a different model of substitution and at a different rate. Current methods can be grouped by the Way the data are handled (genes considered separately or combined into a 'supergene') and the way gene-specific rate models are applied (global versus local clock). There are advantages and disadvantages to each of these approaches, and the optimal method has not yet emerged. Fortunately, time estimates inferred using many genes or proteins have greater precision and appear to be robust to different approaches.
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页码:200 / 206
页数:7
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