Analyzing the microRNA Transcriptome in Plants Using Deep Sequencing Data

Biology

Xiaozeng Yang¹ 

[1] Department of Biology, University of Virginia, Charlottesville VA 22904, USA;

关键词: microRNA;    miRDeep-P;    next-generation sequencing;    small RNA;    plant;   

DOI  :  10.3390/biology1020297

来源: mdpi

【 摘 要 】

MicroRNAs (miRNAs) are 20- to 24-nucleotide endogenous small RNA molecules emerging as an important class of sequence-specific, trans-acting regulators for modulating gene expression at the post-transcription level. There has been a surge of interest in the past decade in identifying miRNAs and profiling their expression pattern using various experimental approaches. In particular, ultra-deep sampling of specifically prepared low-molecular-weight RNA libraries based on next-generation sequencing technologies has been used successfully in diverse species. The challenge now is to effectively deconvolute the complex sequencing data to provide comprehensive and reliable information on the miRNAs, miRNA precursors, and expression profile of miRNA genes. Here we review the recently developed computational tools and their applications in profiling the miRNA transcriptomes, with an emphasis on the model plant Arabidopsis thaliana. Highlighted is also progress and insight into miRNA biology derived from analyzing available deep sequencing data.

【 授权许可】

CC BY   
© 2012 by the authors; licensee MDPI, Basel, Switzerland.