Kinetics of BRCA1 regulation in response to UVC radiation

被引:7
作者
Clarkin, CEK
Zhang, H
Weber, BL [1 ]
机构
[1] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biochem & Mol Biophys, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
关键词
breast cancer; BRCA1; DNA damage; ultraviolet C; MCF-7;
D O I
10.1007/PL00000749
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
To investigate changes in BRCA1 following DNA damage, we exposed MCF-7 cells to increasing doses of ultraviolet C. We observed an increase in BRCA1 protein levels above 78 J/m(2). This increase was observed as early as 5 min after irradiation. BRCA1 levels were then observed to decrease after 2 hi consistent with the previously published data. By pretreating with cycloheximide prior to irradiation, we observed a decrease in the protein half-life, from 3.5 h to 53 min, suggesting that a decrease in protein half-life may cause the lower levels of BRCA1 after irradiation. We also observed an increase in BRCA1 mRNA within 15 min of il radiation, followed by a decrease after 4 h. These data suggest that newly translated protein may contribute to increases in BRCA1 protein levels. The very rapid changes in BRCA1 support its role as a sensor of DNA damage, as opposed to being a repair gene.
引用
收藏
页码:1126 / 1134
页数:9
相关论文
共 37 条
[1]   Regulation of BRCA1 and BRCA2 expression in human breast cancer cells by DNA-damaging agents [J].
Andres, JL ;
Fan, SJ ;
Turkel, GJ ;
Wang, JA ;
Twu, NF ;
Yuan, RQ ;
Lamszus, K ;
Goldberg, ID ;
Rosen, EM .
ONCOGENE, 1998, 16 (17) :2229-2241
[2]  
[Anonymous], 1989, SYNTHETIC OLIGONUCLE
[3]   Fine structural analysis of DNA repair in mammalian cells [J].
Balajee, AS ;
May, A ;
Bohr, VA .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 404 (1-2) :3-11
[4]   UV-induced signal transduction [J].
Bender, K ;
Blattner, C ;
Knebel, A ;
Iordanov, M ;
Herrlich, P ;
Rahmsdorf, HJ .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1997, 37 (1-2) :1-17
[5]   A superfamily of conserved domains in DNA damage responsive cell cycle checkpoint proteins [J].
Bork, P ;
Hofmann, K ;
Bucher, P ;
Neuwald, AF ;
Altschul, SF ;
Koonin, EV .
FASEB JOURNAL, 1997, 11 (01) :68-76
[6]   From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair [J].
Callebaut, I ;
Mornon, JP .
FEBS LETTERS, 1997, 400 (01) :25-30
[7]   Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells [J].
Chen, JJ ;
Silver, DP ;
Walpita, D ;
Cantor, SB ;
Gazdar, AF ;
Tomlinson, G ;
Couch, FJ ;
Weber, BL ;
Ashley, T ;
Livingston, DM ;
Scully, R .
MOLECULAR CELL, 1998, 2 (03) :317-328
[8]  
Chen YM, 1996, CANCER RES, V56, P3168
[9]   Requirement of ATM-dependent phosphorylation of BRCA1 in the DNA damage response to double-strand breaks [J].
Cortez, D ;
Wang, Y ;
Qin, J ;
Elledge, SJ .
SCIENCE, 1999, 286 (5442) :1162-1166
[10]  
deLaat A, 1996, PHOTOCHEM PHOTOBIOL, V63, P492