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基因特异性微小核糖核酸的分离与鉴定。

Isolation and identification of gene-specific microRNAs.

作者信息

Lin Shi-Lung, Chang Donald C, Ying Shao-Yao

机构信息

Division of Regenerative Medicine, WJWU and LYNN Institute for Stem Cell Research, Santa Fe Springs, CA, USA.

出版信息

Methods Mol Biol. 2013;936:271-8. doi: 10.1007/978-1-62703-083-0_21.

Abstract

Computer programming has identified hundreds of genomic hairpin sequences, many with functions remain to be determined. Because direct transfection of hairpin-like miRNA precursors (pre)-miRNAs in mammalian cells is not always sufficient to trigger effective RNA-induced gene silencing complex (RISC) assembly, a key step for RNA interference (RNAi)-related gene silencing, we developed an intronic miRNA-expressing system to overcome this problem by inserting a hairpin-like pre-miRNA structure into the intron region of a gene and successfully increased the efficiency and effectiveness of miRNA-associated RNAi induction in vitro and in vivo. This intronic miRNA biogenesis has been found to depend on a coupled interaction of nascent precursor messenger RNA transcription and intron excision within a specific nuclear region proximal to genomic perichromatin fibrils. The intronic miRNA was transcribed by RNA type II polymerases, coexpressed with a primary gene transcript, and excised out of its encoding gene transcript by intracellular RNA splicing and processing mechanisms. Currently, some ribonuclease III endonucleases have been found to be involved in the processing of spliced introns and probably facilitating the intronic miRNA maturation. Using this miRNA generation system, we have shown for the first time that the intron-derived miRNAs were able to induce strong RNAi effects in not only human and mouse cells but also zebrafishes, chicken embryos, and adult mice. We have also developed an miRNA isolation protocol, based on the complementarity between the designed miRNA and its target gene sequence, to purify and identify the mature miRNAs generated by the intronic miRNA-expressing system. Several intronic miRNA identities and structures are currently confirmed to be active in vitro and in vivo. According to this proven-of-principle method, we now have full knowledge to design pre-miRNA inserts that are more efficient and effective for the intronic miRNA-expressing systems.

摘要

计算机编程已识别出数百个基因组发夹序列,其中许多序列的功能尚待确定。由于在哺乳动物细胞中直接转染类似发夹的微小RNA前体(pre)-miRNA并不总是足以触发有效的RNA诱导基因沉默复合体(RISC)组装,而这是RNA干扰(RNAi)相关基因沉默的关键步骤,因此我们开发了一种内含子miRNA表达系统,通过将类似发夹的pre-miRNA结构插入基因的内含子区域来克服这一问题,并成功提高了体外和体内miRNA相关RNAi诱导的效率和有效性。已发现这种内含子miRNA的生物合成依赖于新生前体信使RNA转录与基因组常染色质纤维近端特定核区域内的内含子切除之间的耦合相互作用。内含子miRNA由RNA II型聚合酶转录,与初级基因转录本共表达,并通过细胞内RNA剪接和加工机制从其编码基因转录本中切除。目前,已发现一些核糖核酸酶III内切酶参与剪接内含子的加工,并可能促进内含子miRNA的成熟。使用这种miRNA生成系统,我们首次表明,内含子衍生的miRNA不仅能够在人和小鼠细胞中,还能在斑马鱼、鸡胚胎和成年小鼠中诱导强烈的RNAi效应。我们还基于设计的miRNA与其靶基因序列之间的互补性,开发了一种miRNA分离方案,以纯化和鉴定由内含子miRNA表达系统产生的成熟miRNA。目前已证实几种内含子miRNA的身份和结构在体外和体内均具有活性。根据这种原理验证方法,我们现在完全有能力设计对内含子miRNA表达系统更高效的pre-miRNA插入片段。

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