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通过mRAP分析微小RNA的表达

Profiling of microRNA expression by mRAP.

作者信息

Takada Shuji, Mano Hiroyuki

机构信息

Division of Functional Genomics, Jichi Medical University, 3311-1 Yakushiji, Shimotsukeshi, Tochigi 329-0498, Japan.

出版信息

Nat Protoc. 2007;2(12):3136-45. doi: 10.1038/nprot.2007.457.

Abstract

MicroRNA (miRNA) amplification profiling (mRAP) is a sensitive method for the determination of miRNA expression profiles. The method relies on a long, optimized 5' adaptor and the SMART (switching mechanism at the 5' end of RNA templates of reverse transcriptase) reaction to yield miRNA-derived cDNAs flanked by synthesized oligomers at each end. The cDNAs are PCR-amplified with primers corresponding to the oligomers, and the products are concatamerized for nucleotide sequencing. The expression level of each miRNA can be estimated from the frequency of the occurrence of its sequence in the data set, provided that sufficient clones of the cDNAs are sequenced. This method potentially yields millions of miRNA-derived clones from as few as 1 x 10(4) cells, thus allowing the characterization of miRNA expression profiles with small quantities of starting material such as those available for fresh clinical specimens or organs of developing embryos. This protocol can be completed in 10 d.

摘要

微小RNA(miRNA)扩增分析(mRAP)是一种用于确定miRNA表达谱的灵敏方法。该方法依赖于一个长的、经过优化的5'接头和SMART(逆转录酶RNA模板5'端的切换机制)反应,以产生两端由合成寡聚物侧翼的miRNA衍生cDNA。用与寡聚物对应的引物对cDNA进行PCR扩增,并将产物连接起来进行核苷酸测序。只要对足够数量的cDNA克隆进行测序,就可以根据其序列在数据集中出现的频率来估计每个miRNA的表达水平。该方法有可能从少至1×10⁴个细胞中产生数百万个miRNA衍生克隆,从而能够用少量起始材料(如新鲜临床标本或发育中胚胎的器官中可得的材料)来表征miRNA表达谱。本方案可在10天内完成。

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