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Mammalian 5'-Capped MicroRNA Precursors that Generate a Single MicroRNA

机译:产生单个MicroRNA的哺乳动物5'帽MicroRNA前体

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摘要

MicroRNAs (miRNAs) are short RNA gene regulators typically produced from primary transcripts that are cleaved by the nuclear microprocessor complex, with the resulting precursor miRNA hairpins exported by exportin 5 and processed by cytoplasmic Dicer to yield two (5p and 3p) miRNAs. Here, we document microprocessor-independent 7-methylguanosine (m~7G)-capped pre-miRNAs, whose 5' ends coincide with transcription start sites and 3' ends are most likely generated by transcription termination. By stablishing a small RNA Cap-seq method that employs the cap-binding protein elF4E, we identified a group of urine m~7G-capped pre-miRNAs genome wide. The m~7G-capped pre-miRNAs are exported via the PHAX-exportin 1 pathway. After Dicer cleavage, only the 3p-miRNA is efficiently loaded onto Argonaute to form a functional microRNP. This unusual miRNA biogenesis pathway, which differs in pre-miRNA synthesis, nuclear-cytoplasmic transport, and guide strand selection, enables the development of shRNA expression constructs that produce a single 3p-siRNA.
机译:微小RNA(miRNA)是短RNA基因调节子,通常由被核微处理器复合物切割的初级转录产物产生,所得的前体miRNA发夹由exportin 5输出并由细胞质切块机加工以产生两个(5p和3p)miRNA。在这里,我们记录了独立于微处理器的7-甲基鸟苷(m〜7G)封闭的pre-miRNA,其5'末端与转录起始位点重合,而3'末端最有可能由转录终止产生。通过建立一个采用帽结合蛋白elF4E的小RNA Cap-seq方法,我们确定了一组尿液,覆盖了整个m〜7G的pre-miRNA基因组。 m〜7G封闭的pre-miRNA通过PHAX-exportin 1途径输出。在切丁酶切割后,仅将3p-miRNA有效地加载到Argonaute上以形成功能性microRNP。这种不寻常的miRNA生物发生途径在pre-miRNA合成,核质运输和引导链选择方面有所不同,从而能够开发产生单个3p-siRNA的shRNA表达构建体。

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