Biogenesis and Transcriptional Regulation of Long Noncoding RNAs in the Human Immune System

被引:35
|
作者
Spurlock, Charles F., III [1 ]
Crooke, Philip S., III [2 ]
Aune, Thomas M. [1 ]
机构
[1] Vanderbilt Univ, Dept Med, Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Math, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
SUPER-ENHANCERS; B-CELL; FUNCTIONAL-ANALYSIS; GENE-EXPRESSION; CHROMATIN; REVEALS; ACTIVATION; PRINCIPLES; DISCOVERY; EVOLUTION;
D O I
10.4049/jimmunol.1600970
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The central dogma of molecular biology states that DNA makes RNA makes protein. Discoveries over the last quarter of a century found that the process of DNA transcription into RNA gives rise to a diverse array of functional RNA species, including genes that code for protein and noncoding RNAs. For decades, the focus has been on understanding how protein-coding genes are regulated to influence protein expression. However, with the completion of the Human Genome Project and follow-up ENCODE data, it is now appreciated that only 2-3% of the genome codes for protein-coding gene exons and that the bulk of the transcribed genome, apart from ribosomal RNAs, is at the level of noncoding RNA genes. In this article, we focus on the biogenesis and regulation of a distinct class of noncoding RNA molecules termed long, noncoding RNAs in the context of the immune system.
引用
收藏
页码:4509 / 4517
页数:9
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