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Genomic competition for noise reduction shaped evolutionary landscape of mir-4673

机译:MIR-4673降噪形状浮雕景观的基因组竞争

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The genomic platform that informs evolution of microRNA cascades remains unknown. Here we capitalised on the recent evolutionary trajectory of hominin-specific miRNA-4673, encoded in intron 4 of notch-1, to uncover the identity of one such precursor genomic element and the selective forces acting upon it. The miRNA targets genes that regulate Wnt/β-catenin signalling cascade. Primary sequence of the microRNA and its target region in Wnt modulating genes evolved from homologous signatures mapped to homotypic cis-clusters recognised by TCF3/4 and TFAP2A/B/C families. Integration of homologous TFAP2A/B/C cis-clusters (short range inhibitor of β-catenin) into the transcriptional landscape of Wnt cascade genes can reduce noise in gene expression. Probabilistic adoption of miRNA secondary structure by one such cis-signature in notch-1 reflected selection for superhelical curvature symmetry of precursor DNA to localise a nucleosome that overlapped the latter cis-cluster. By replicating the cis-cluster signature, non-random interactions of the miRNA with key Wnt modulator genes expanded the transcriptional noise buffering capacity via a coherent feed-forward loop mechanism. In consequence, an autonomous transcriptional noise dampener (the cis-cluster/nucleosome) evolved into a post-transcriptional one (the miRNA). The findings suggest a latent potential for remodelling of transcriptional landscape by miRNAs that capitalise on non-random distribution of genomic cis-signatures.
机译:告知MicroRNA级联演变的基因组平台仍然未知。在这里,我们利用了在Notch-1的Intron 4中编码的原始特异性miRNA-4673的最近进化轨迹,以揭示一种这样的前体基因组元素的同一性和作用在其上的选择性。 miRNA靶向调节Wnt /β-catenin信号传导级联的基因。 MicroRNA的主要序列及其靶区域在WNT调节基因中从映射到由TCF3 / 4和TFAP2A / B / C系列识别的同型CIS簇的同源签名中演变。将同源TFAP2A / B / C CIS-簇的整合(β-CAT键的短程抑制剂)进入WNT级联基因的转录景观可以降低基因表达中的噪声。在Notch-1中的一种这样的顺式签名中的概率采用MiRNA二次结构,反映选择前体DNA的超异形曲率对称性,以定位重叠后者CIS簇的核小体。通过对CIS-Cluster签名进行复制,MiRNA与键WNT调制器基因的非随机相互作用通过相干前馈回路机构扩展了转录噪声缓冲能力。结果,一种自主转录噪声阻尼器(CIS-簇/核小体)演变成转录后一种(miRNA)。研究结果表明,MIRNA通过利用基因组CIS-签名的非随机分布来重塑的潜在潜力。

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