4.8 Article

Selection on Synonymous Sites for Increased Accessibility around miRNA Binding Sites in Plants

期刊

MOLECULAR BIOLOGY AND EVOLUTION
卷 29, 期 10, 页码 3037-3044

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molbev/mss109

关键词

synonymous selection; microRNA function; site accessibility

资金

  1. National Basic Research Program of China [2012CB316501]
  2. National High Technology Research and Development Program of China (863 Project) [2012AA020401]
  3. National Natural Science Foundation of China [30900836, 61171143, 61001175]
  4. Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry, China

向作者/读者索取更多资源

Synonymous codons are widely selected for various biological mechanisms in both prokaryotes and eukaryotes. Recent evidence suggests that microRNA (miRNA) function may affect synonymous codon choices near miRNA target sites. To better understand this, we perform genome-wide analysis on synonymous codon usage around miRNA target sites in four plant genomes. We observed a general trend of increased site accessibility around miRNA target sites in plants. Guanine-cytosine (GC)-poor codons are preferred in the flank region of miRNA target sites. Within-genome analyses show significant variation among miRNA targets in species. GC content of the target gene can partly explain the variation of site accessibility among miRNA targets. miRNA targets in GC-rich genes show stronger selection signals than those in GC-poor genes. Gene's codon usage bias and the conservation level of miRNA and its target also have some effects on site accessibility, but the expression level of miRNA or its target and the mechanism of miRNA activity do not contribute to site accessibility differences among miRNA targets. We suggest that synonymous codons near miRNA targets are selected for efficient miRNA binding and proper miRNA function. Our results present a new dimension of natural selection on synonymous codons near miRNA target sites in plants, which will have important implications of coding sequence evolution.

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