BRCA1 regulates the interferon γ-mediated apoptotic response

被引:62
作者
Andrews, HN
Mullan, PB
McWilliams, S
Sebelova, S
Quinn, JE
Gilmore, PM
McCabe, N
Pace, A
Koller, B
Johnston, PG
Haber, DA
Harkin, DP
机构
[1] Queens Univ Belfast, Dept Oncol, Canc Res Ctr, Belfast BT9 7AB, Antrim, North Ireland
[2] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[3] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
[4] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
关键词
D O I
10.1074/jbc.M201316200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BRCA1 is a tumor suppressor gene implicated in transcriptional regulation. We have generated cell lines with inducible expression of BRCA1 as a tool to identify downstream targets that may be important mediators of BRCA1 function. Oligonucleotide array-based expression profiling identified 11 previously described interferon regulated genes that were up-regulated following inducible expression of BRCA1. Northern blot analysis revealed that a subset of the identified targets including IRF-7, MxA, and ISG-54 were synergistically up-regulated by BRCA1 in the presence of interferon gamma (IFN-gamma) but not interferons alpha or beta. Importantly, IFN-gamma-mediated induction of IRF-7 and MxA was attenuated in the BRCA1 mutant cell line HCC1937, an effect that was rescued following reconstitution of exogenous wild type BRCA1 in these cells. Furthermore, reconstituted BRCA1 sensitized HCC1937 cells to IFN-gamma-induced apoptotic cell death. This study identifies BRCA1 as a component of the IFN-gamma-regulated signaling pathway and suggests that BRCA1 may play a role in the regulation of IFN-gamma-mediated apoptosis.
引用
收藏
页码:26225 / 26232
页数:8
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