On the Expansion of "Dangerous'' Gene Repertoires by Whole-Genome Duplications in Early Vertebrates

被引:38
|
作者
Singh, Param Priya [1 ]
Affeldt, Severine [1 ]
Cascone, Ilaria [2 ]
Selimoglu, Rasim [2 ]
Camonis, Jacques [2 ]
Isambert, Herve [1 ]
机构
[1] UPMC, Inst Curie, Res Ctr, CNRS,UMR168, F-75248 Paris, France
[2] UPMC, Inst Curie, Res Ctr, INSERM,U830, F-75248 Paris, France
来源
CELL REPORTS | 2012年 / 2卷 / 05期
关键词
YEAST RIBOSOMAL-PROTEINS; DISEASE GENES; TUMOR-FORMATION; COPY NUMBER; RAS GENE; H-RAS; DOSAGE; EVOLUTION; SELECTION; DISPENSABILITY;
D O I
10.1016/j.celrep.2012.09.034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The emergence and evolutionary expansion of gene families implicated in cancers and other severe genetic diseases is an evolutionary oddity from a natural selection perspective. Here, we show that gene families prone to deleterious mutations in the human genome have been preferentially expanded by the retention of "ohnolog'' genes from two rounds of whole-genome duplication (WGD) dating back from the onset of jawed vertebrates. We further demonstrate that the retention of many ohnologs suspected to be dosage balanced is in fact indirectly mediated by their susceptibility to deleterious mutations. This enhanced retention of "dangerous'' ohnologs, defined as prone to autosomal-dominant deleterious mutations, is shown to be a consequence of WGD-induced speciation and the ensuing purifying selection in post-WGD species. These findings highlight the importance of WGD-induced nonadaptive selection for the emergence of vertebrate complexity, while rationalizing, from an evolutionary perspective, the expansion of gene families frequently implicated in genetic disorders and cancers.
引用
收藏
页码:1387 / 1398
页数:12
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