4.8 Article

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

Journal

NATURE GENETICS
Volume 43, Issue 7, Pages 621-U196

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ng.848

Keywords

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Funding

  1. US National Institutes of Health (NIH)/National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) [K08-AR054615]
  2. NIH/National Cancer Institute (NCI) [R01-CA118750, R01-CA130795]
  3. Juvenile Diabetes Research Foundation
  4. American Cancer Society
  5. Stanford Graduate Fellowship
  6. National Science Foundation (NSF)
  7. Department of Defense (DoD)
  8. Grants-in-Aid for Scientific Research [22115508] Funding Source: KAKEN

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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.

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