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EMBO Rep. 2015 Nov;16(11):1520-34. doi: 10.15252/embr.201540437. Epub 2015 Sep 27.

A BRCA1-interacting lncRNA regulates homologous recombination.

Author information

1
National Cancer Institute, NIH, Bethesda, MD, USA viveksharmabt@gmail.com mistelit@mail.nih.gov.
2
National Cancer Institute, NIH, Bethesda, MD, USA.
3
National Institute on Aging, NIH, Baltimore, MD, USA.

Abstract

Long non-coding RNAs (lncRNAs) are important players in diverse biological processes. Upon DNA damage, cells activate a complex signaling cascade referred to as the DNA damage response (DDR). Using a microarray screen, we identify here a novel lncRNA, DDSR1 (DNA damage-sensitive RNA1), which is induced upon DNA damage. DDSR1 induction is triggered in an ATM-NF-κB pathway-dependent manner by several DNA double-strand break (DSB) agents. Loss of DDSR1 impairs cell proliferation and DDR signaling and reduces DNA repair capacity by homologous recombination (HR). The HR defect in the absence of DDSR1 is marked by aberrant accumulation of BRCA1 and RAP80 at DSB sites. In line with a role in regulating HR, DDSR1 interacts with BRCA1 and hnRNPUL1, an RNA-binding protein involved in DNA end resection. Our results suggest a role for the lncRNA DDSR1 in modulating DNA repair by HR.

KEYWORDS:

BRCA1; RAP80; hnRNPUL1; p53; repair

Comment in

PMID:
26412854
PMCID:
PMC4641504
DOI:
10.15252/embr.201540437
[Indexed for MEDLINE]
Free PMC Article

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