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利用大小编码连接介导 PCR 分析 microRNA 特征。

Analysis of microRNA signatures using size-coded ligation-mediated PCR.

机构信息

Department of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, Tehran 1585636473, Iran.

出版信息

Nucleic Acids Res. 2011 Jul;39(12):e80. doi: 10.1093/nar/gkr214. Epub 2011 Apr 12.

Abstract

The expression pattern and regulatory functions of microRNAs (miRNAs) are intensively investigated in various tissues, cell types and disorders. Differential miRNA expression signatures have been revealed in healthy and unhealthy tissues using high-throughput profiling methods. For further analyses of miRNA signatures in biological samples, we describe here a simple and efficient method to detect multiple miRNAs simultaneously in total RNA. The size-coded ligation-mediated polymerase chain reaction (SL-PCR) method is based on size-coded DNA probe hybridization in solution, followed-by ligation, PCR amplification and gel fractionation. The new method shows quantitative and specific detection of miRNAs. We profiled miRNAs of the let-7 family in a number of organisms, tissues and cell types and the results correspond with their incidence in the genome and reported expression levels. Finally, SL-PCR detected let-7 expression changes in human embryonic stem cells as they differentiate to neuron and also in young and aged mice brain and bone marrow. We conclude that the method can efficiently reveal miRNA signatures in a range of biological samples.

摘要

微 RNA(miRNA)的表达模式和调控功能在各种组织、细胞类型和疾病中都得到了深入研究。使用高通量分析方法已经揭示了健康和不健康组织中 miRNA 的差异表达谱。为了进一步分析生物样本中的 miRNA 特征,我们在这里描述了一种简单而有效的方法,可用于在总 RNA 中同时检测多个 miRNA。基于大小编码 DNA 探针杂交的连接介导聚合酶链反应(SL-PCR)方法,随后进行连接、PCR 扩增和凝胶分离。该新方法显示了 miRNA 的定量和特异性检测。我们对许多生物体、组织和细胞类型中的 let-7 家族 miRNA 进行了分析,结果与它们在基因组中的出现和报道的表达水平相对应。最后,SL-PCR 检测了人类胚胎干细胞向神经元分化过程中 let-7 的表达变化,以及年轻和老年小鼠大脑和骨髓中的表达变化。我们得出结论,该方法可以有效地揭示一系列生物样本中的 miRNA 特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d404/3130289/d22481eec9fc/gkr214f1.jpg

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