Uncovering the role of genomic "dark matter" in human disease

被引:64
|
作者
Martin, Lance [1 ,2 ,3 ]
Chang, Howard Y. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2012年 / 122卷 / 05期
关键词
LONG NONCODING RNA; HEPATOCELLULAR-CARCINOMA; MESSENGER-RNAS; ALU RNA; GENE; CANCER; CHROMATIN; EXPRESSION; IDENTIFICATION; TRANSCRIPTION;
D O I
10.1172/JCI60020
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The human genome encodes thousands of long noncociing RNAs (IncRNAs). Although most remain functionally uncharacterized biological "dark matter," IncRNAs have garnered considerable attention for their diverse roles in human biology, including developmental programs and tumor suppressor gene networks. As the number of IncRNAs associated with human disease grows, ongoing research efforts are focusing on their regulatory mechanisms. New technologies that enable enumeration of IncRNA interaction partners and determination of lncRNA structure are well positioned to drive deeper understanding of their functions and involvement in pathogenesis. In turn, lncRNAs may become targets for therapeutic intervention or new tools for biotechnology.
引用
收藏
页码:1589 / 1595
页数:7
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