The molecular basis of phenotypic evolution: beyond the usual suspects

被引:2
|
作者
Lin, Rong-Chien [1 ]
Ferreira, Bianca T. [1 ]
Yuan, Yao-Wu [1 ]
机构
[1] Univ Connecticut, Dept Ecol & Evolutionary Biol, Storrs, CT 06269 USA
关键词
OPEN READING FRAMES; EVO-DEVO; GENE; PROTEIN; SUPERGENE; LOCUS; NEOFUNCTIONALIZATION; BIOGENESIS; SPECIATION; INSERTION;
D O I
10.1016/j.tig.2024.04.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It has been well documented that mutations in coding DNA or cis-regulatory elements underlie natural phenotypic variation in many organisms. However, the development of sophisticated functional tools in recent years in a wide range of traditionally non-model systems have revealed many 'unusual suspects' in the molecular bases of phenotypic evolution, including upstream open reading frames (uORFs), cryptic splice sites, and small RNAs. Furthermore, large-scale genome sequencing, especially long-read sequencing, has identified a cornucopia of structural variation underlying phenotypic divergence and elucidated the composition of supergenes that control complex multi-trait polymorphisms. In this review article we highlight recent studies that demonstrate this great diversity of molecular mechanisms producing adaptive genetic variation and the panoply of evolutionary paths leading to the 'grandeur of life'.
引用
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页码:668 / 680
页数:13
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