the impact of mirna target sites in coding sequences and in 3′utrsmicrorna的目标站点的影响在编码序列和3u2032utr.pdfVIP

the impact of mirna target sites in coding sequences and in 3′utrsmicrorna的目标站点的影响在编码序列和3u2032utr.pdf

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the impact of mirna target sites in coding sequences and in 3′utrsmicrorna的目标站点的影响在编码序列和3u2032utr

The Impact of miRNA Target Sites in Coding Sequences and in 39UTRs Zhuo Fang, Nikolaus Rajewsky* ¨ ¨ Max Delbruck Centrum fur Molekulare Medizin, Berlin, Germany Abstract Animal miRNAs are a large class of small regulatory RNAs that are known to directly and negatively regulate the expression of a large fraction of all protein encoding genes. The identification and characterization of miRNA targets is thus a fundamental problem in biology. miRNAs regulate target genes by binding to 39 untranslated regions (39UTRs) of target mRNAs, and multiple binding sites for the same miRNA in 39UTRs can strongly enhance the degree of regulation. Recent experiments have demonstrated that a large fraction of miRNA binding sites reside in coding sequences. Overall, miRNA binding sites in coding regions were shown to mediate smaller regulation than 39UTR binding. However, possible interactions between target sites in coding sequences and 39UTRs have not been studied. Using transcriptomics and proteomics data of ten miRNA mis-expression experiments as well as transcriptome-wide experimentally identified miRNA target sites, we found that mRNA and protein expression of genes containing target sites both in coding regions and 39UTRs were in general mildly but significantly more regulated than those containing target sites in 39UTRs only. These effects were stronger for conserved target sites of length 7– 8 nt in coding regions compared to non-conserved sites. Combined with our other finding that miRNA target sites in coding regions are under negative selection, our results shed light on the functional importance of miRNA targeting in coding regions. Citation: Fang Z, Rajewsky N (2011) The Impact of miRNA Target Sites in Coding Sequences and in 39UTRs. PLoS ONE 6(3): e18067. doi:10.1371/ journal.pone.0018067 Editor: Sumitra Deb, Virginia Com

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