z-logo
Premium
A BRCA 1‐interacting lnc RNA regulates homologous recombination
Author(s) -
Sharma Vivek,
Khurana Simran,
Kubben Nard,
Abdelmohsen Kotb,
Oberdoerffer Philipp,
Gorospe Myriam,
Misteli Tom
Publication year - 2015
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.15252/embr.201540437
Subject(s) - homologous recombination , homologous chromosome , rna , microbiology and biotechnology , biology , genetics , gene
Long non‐coding RNA s (lnc RNA s) 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 lnc RNA , DDSR 1 ( DNA damage‐sensitive RNA 1), which is induced upon DNA damage. DDSR 1 induction is triggered in an ATM ‐ NF ‐ κB pathway‐dependent manner by several DNA double‐strand break ( DSB ) agents. Loss of DDSR 1 impairs cell proliferation and DDR signaling and reduces DNA repair capacity by homologous recombination ( HR ). The HR defect in the absence of DDSR 1 is marked by aberrant accumulation of BRCA 1 and RAP 80 at DSB sites. In line with a role in regulating HR , DDSR 1 interacts with BRCA 1 and hn RNPUL 1, an RNA ‐binding protein involved in DNA end resection. Our results suggest a role for the lnc RNA DDSR 1 in modulating DNA repair by HR .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom