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Human microRNAs in host–parasite interaction: a review

机译:寄生虫互动中的人体microRNA:综述

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摘要

The canonical pathway of miRNA biogenesis. a In the nucleus, the miRNA gene is transcribed by RNA polymerase II and then fold into a long pri-miRNA with a hairpin structure. The long pri-miRNA is then cleaved by the microprocessor complex made up of Drosha and DGCR8 (Pasha) proteins, generating a precursor miRNA (pre-miRNA). b Exportin-5 binds to the pre-miRNA and facilitates its export to the cytoplasm. In the cytoplasm, the type III RNase Dicer complex with the double-stranded RNA binding protein TRBP and PACT cleaves the precursor’s hairpin and the resulting duplex is isolated by a helicase enzyme. Finally, the functional strand is loaded together with the Argonaute (AGO) protein into the RNA-induced silencing complex (RISC) to target mRNAs by sequence complementary binding and mediates gene suppression through mechanisms of either translational repression or mRNA degradation
机译:miRNA生物发生的规范途径。在核中,MiRNA基因通过RNA聚合酶II转录,然后用发夹结构折叠到长期pri-miRNA中。然后通过由DROSHA和DGCR8(PASHA)蛋白组成的微处理器络合物来切割长期pRI-miRNA,产生前体miRNA(预-miRNA)。 B导出-5与前miRNA结合,促进其出口到细胞质。在细胞质中,具有双链RNA结合蛋白Trbp和Pact的III型RNase Dicer络合物和Pact粘合前体的发夹,并通过螺旋酶分离所得的双链体。最后,用序列互补结合和介导基因抑制通过翻译抑制或mRNA降解的机制,将函数链与Argonaute(前)蛋白加载到RNA诱导的沉默复合物(RISC)中以靶向MRNA,并介导基因抑制或MRNA降解的机制

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