Human disease genes: patterns and predictions

被引:76
|
作者
Smith, NGC
Eyre-Walker, A
机构
[1] Uppsala Univ, Evolutionary Biol Ctr, Dept Evolut Biol, S-75236 Uppsala, Sweden
[2] Univ Sussex, Ctr Study Evolut, Brighton, E Sussex, England
[3] Univ Sussex, Sch Biol Sci, Brighton, E Sussex, England
关键词
deleterious mutations; nearly neutral theory; substitution rate variation; protein function; nonsynonymous/synonymous rate ratio; human disease gene prediction;
D O I
10.1016/S0378-1119(03)00772-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We compared genes at which mutations are known to cause human disease (disease genes) with other human genes (nondisease genes) using a large set of human-rodent alignments to infer evolutionary patterns. Such comparisons may be of use both in predicting disease genes and in understanding the general evolution of human genes. Four features were found to differ significantly between disease and nondisease genes, with disease genes (i) evolving with higher nonsynonymous/synonymous substitution rate ratios (Ka/Ks), (ii) evolving at higher synonymous substitution rates, (iii) with longer protein-coding sequences, and (iv) expressed in a narrower range of tissues. Discriminant analysis showed that these differences may help to predict human disease genes. We also investigated other factors affecting the mode of evolution in the disease genes: Ka/Ks is significantly affected by protein function, mode of inheritance, and the reduction of life expectancy caused by disease. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 175
页数:7
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