Understanding the transcriptome through RNA structure

被引:350
作者
Wan, Yue [1 ,2 ]
Kertesz, Michael [3 ]
Spitale, Robert C. [1 ,2 ]
Segal, Eran [4 ,5 ]
Chang, Howard Y. [1 ,2 ]
机构
[1] Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Program Epithelial Biol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[4] Weizmann Inst Sci, IL-76100 Rehovot, Israel
[5] Dept Comp Sci & Appl Math, IL-76100 Rehovot, Israel
基金
美国国家卫生研究院;
关键词
SECONDARY STRUCTURE PREDICTION; SELECTIVE 2'-HYDROXYL ACYLATION; DYNAMIC-PROGRAMMING ALGORITHM; MESSENGER-RNA; GENE-EXPRESSION; THERMODYNAMIC PARAMETERS; WIDE IDENTIFICATION; CRYSTAL-STRUCTURES; BACILLUS-SUBTILIS; STRUCTURE MOTIFS;
D O I
10.1038/nrg3049
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
RNA structure is crucial for gene regulation and function. In the past, transcriptomes have largely been parsed by primary sequences and expression levels, but it is now becoming feasible to annotate and compare transcriptomes based on RNA structure. In addition to computational prediction methods, the recent advent of experimental techniques to probe RNA structure by high-throughput sequencing has enabled genome-wide measurements of RNA structure and has provided the first picture of the structural organization of a eukaryotic transcriptome - the 'RNA structurome'. With additional advances in method refinement and interpretation, structural views of the transcriptome should help to identify and validate regulatory RNA motifs that are involved in diverse cellular processes and thereby increase understanding of RNA function.
引用
收藏
页码:641 / 655
页数:15
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