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通过深度平行测序发现植物微小RNA和短干扰RNA

Discovery of plant microRNAs and short-interfering RNAs by deep parallel sequencing.

作者信息

Chellappan Padmanabhan, Jin Hailing

机构信息

Department of Plant Pathology and Microbiology, Center for Plant Cell Biology, Institute for Integrative Genome Biology, University of California Riverside, CA, USA.

出版信息

Methods Mol Biol. 2009;495:121-32. doi: 10.1007/978-1-59745-477-3_11.

Abstract

Endogenous small RNAs, including microRNAs (miRNAs) and small interfering RNAs (siRNAs), play important regulatory roles in development, hormone signaling, stress responses, and genome stability. These small RNAs induce transcriptional or posttranscriptional gene silencing by guiding heterochromatin formation, mRNA degradation, or translational inhibition. In this chapter, we describe the methods for small RNA discovery in plants by small RNA cloning and deep parallel sequencing. We compare two methods of small RNA library construction: the 5' phosphate (P)-independent and 5' phosphate (P)-dependent methods. Deep parallel sequencing of small RNA libraries is discussed by comparing among 454, SBS, and SOLiD technologies.

摘要

内源性小RNA,包括微小RNA(miRNA)和小干扰RNA(siRNA),在发育、激素信号传导、应激反应和基因组稳定性中发挥重要的调节作用。这些小RNA通过引导异染色质形成、mRNA降解或翻译抑制来诱导转录或转录后基因沉默。在本章中,我们描述了通过小RNA克隆和深度平行测序在植物中发现小RNA的方法。我们比较了两种小RNA文库构建方法:5'磷酸(P)非依赖性和5'磷酸(P)依赖性方法。通过比较454、SBS和SOLiD技术来讨论小RNA文库的深度平行测序。

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