Extensive and coordinated transcription of noncoding RNAs within cell-cycle promoters

被引:967
作者
Hung, Tiffany [1 ,2 ]
Wang, Yulei [3 ]
Lin, Michael F. [4 ,5 ]
Koegel, Ashley K. [1 ,2 ]
Kotake, Yojiro [6 ,7 ,8 ]
Grant, Gavin D. [9 ]
Horlings, Hugo M. [10 ]
Shah, Nilay [11 ]
Umbricht, Christopher [12 ]
Wang, Pei [13 ]
Wang, Yu [3 ]
Kong, Benjamin [3 ]
Langerod, Anita [14 ]
Borresen-Dale, Anne-Lise [14 ,15 ]
Kim, Seung K. [2 ,13 ]
van de Vijver, Marc [10 ]
Sukumar, Saraswati [11 ]
Whitfield, Michael L. [9 ]
Kellis, Manolis [4 ,5 ]
Xiong, Yue [6 ]
Wong, David J. [1 ]
Chang, Howard Y. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[3] Life Technol, Foster City, CA USA
[4] Broad Inst, Cambridge, MA USA
[5] MIT, Comp Sci & Artificial Intelligence Lab, Cambridge, MA 02139 USA
[6] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[7] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC USA
[8] Hamamatsu Univ Sch Med, Dept Biochem 1, Higashi Ku, Hamamatsu, Shizuoka 4313192, Japan
[9] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Genet, Hanover, NH 03756 USA
[10] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
[11] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[12] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
[13] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[14] Oslo Univ Hosp, Radiumhosp, Dept Genet, Inst Canc Res, Oslo, Norway
[15] Univ Oslo, Fac Med, Inst Clin Med, Oslo, Norway
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENE-EXPRESSION; HUMAN FIBROBLASTS; CDK INHIBITORS; BREAST-CANCER; MODULE MAP; GENOME; IDENTIFICATION; DEMARCATION; CHECKPOINTS; INITIATION;
D O I
10.1038/ng.848
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Transcription of long noncoding RNAs (lncRNAs) within gene regulatory elements can modulate gene activity in response to external stimuli, but the scope and functions of such activity are not known. Here we use an ultrahigh-density array that tiles the promoters of 56 cell-cycle genes to interrogate 108 samples representing diverse perturbations. We identify 216 transcribed regions that encode putative lncRNAs, many with RT-PCR-validated periodic expression during the cell cycle, show altered expression in human cancers and are regulated in expression by specific oncogenic stimuli, stem cell differentiation or DNA damage. DNA damage induces five lncRNAs from the CDKN1A promoter, and one such lncRNA, named PANDA, is induced in a p53-dependent manner. PANDA interacts with the transcription factor NF-YA to limit expression of pro-apoptotic genes; PANDA depletion markedly sensitized human fibroblasts to apoptosis by doxorubicin. These findings suggest potentially widespread roles for promoter lncRNAs in cell-growth control.
引用
收藏
页码:621 / U196
页数:11
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