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A search for conserved sequences in coding regions reveals that the let-7 microRNA targets Dicer within its coding sequence

机译:在编码区中保守序列的搜索显示let-7 microRNA在其编码序列内靶向Dicer

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摘要

Recognition sites for microRNAs (miRNAs) have been reported to be located in the 3′ untranslated regions of transcripts. In a computational screen for highly conserved motifs within coding regions, we found an excess of sequences conserved at the nucleotide level within coding regions in the human genome, the highest scoring of which are enriched for miRNA target sequences. To validate our results, we experimentally demonstrated that the let-7 miRNA directly targets the miRNA-processing enzyme Dicer within its coding sequence, thus establishing a mechanism for a miRNA/Dicer autoregulatory negative feedback loop. We also found computational evidence to suggest that miRNA target sites in coding regions and 3′ UTRs may differ in mechanism. This work demonstrates that miRNAs can directly target transcripts within their coding region in animals, and it suggests that a complete search for the regulatory targets of miRNAs should be expanded to include genes with recognition sites within their coding regions. As more genomes are sequenced, the methodological approach that we used for identifying motifs with high sequence conservation will be increasingly valuable for detecting functional sequence motifs within coding regions.
机译:据报道,microRNA(miRNA)的识别位点位于转录本的3'非翻译区。在编码区域内高度保守的基序的计算筛选中,我们发现了人类基因组编码区域内核苷酸水平保守的过量序列,其最高得分富含miRNA目标序列。为了验证我们的结果,我们实验证明了let-7 miRNA在其编码序列内直接靶向miRNA加工酶Dicer,从而建立了miRNA / Dicer自动调节负反馈回路的机制。我们还发现计算证据表明,编码区和3'UTRs中的miRNA靶位点可能在机制上有所不同。这项工作表明,miRNA可以直接在动物的编码区域内靶向转录物,并建议应扩大对miRNA调控靶标的完全搜索,以包括在其编码区域内具有识别位点的基因。随着更多的基因组被测序,我们用于鉴定具有高度序列保守性的基序的方法学方法对于检测编码区内的功能性序列基序将越来越有价值。

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