Positive regulation of the BRCA1 promoter

被引:44
作者
Thakur, S
Croce, CM
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Kimmel Canc Inst, Philadelphia, PA 19107 USA
关键词
D O I
10.1074/jbc.274.13.8837
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
Inherited mutations in the BRCA1 gene, presumably leading to loss of function, confer susceptibility to breast and ovarian neoplasms and are thought to be responsible for approximately 2.5-5% of all breast cancers. It has been suggested that alternative mechanisms, such as disruption of transcription, may also be involved in the suppression of BRCA1 gene expression/ function in breast cancers. Therefore, we initiated studies on the BRCA1 transcriptional promoter. Utilizing systematic promoter deletions and transient transfection assays, a 36-base pair region was determined to be important for the positive regulation of BRCA1 transcription. Deletion of this positive regulatory region resulted in a significant loss of promoter activity. Utilizing DNA binding assays, proteins with specific affinities for the positive regulatory region were detected. Disruption of the DNA-protein complexes could affect normal BRCA1 transcription and may contribute to breast cancer susceptibility.
引用
收藏
页码:8837 / 8843
页数:7
相关论文
共 31 条
[21]   FAMILY HISTORY AND THE RISK OF BREAST-CANCER [J].
SATTIN, RW ;
RUBIN, GL ;
WEBSTER, LA ;
HUEZO, CM ;
WINGO, PA ;
ORY, HW ;
LAYDE, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1985, 253 (13) :1908-1913
[22]   Association of BRCA1 with Rad51 in mitotic and meiotic cells [J].
Scully, R ;
Chen, JJ ;
Plug, A ;
Xiao, YH ;
Weaver, D ;
Feunteun, J ;
Ashley, T ;
Livingston, DM .
CELL, 1997, 88 (02) :265-275
[23]   Dynamic changes of BRCA1 subnuclear location and phosphorylation state are initiated by DNA damage [J].
Scully, R ;
Chen, JJ ;
Ochs, RL ;
Keegan, K ;
Hoekstra, M ;
Feunteun, J ;
Livingston, DM .
CELL, 1997, 90 (03) :425-435
[24]   BRCA1 is a component of the RNA polymerase II holoenzyme [J].
Scully, R ;
Anderson, SF ;
Chao, DM ;
Wei, WJ ;
Ye, LY ;
Young, RA ;
Livingston, DM ;
Parvin, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5605-5610
[25]   Decreased BRCA1 expression levels may arrest the cell cycle through activation of p53 checkpoint in human sporadic breast tumors [J].
Sourvinos, G ;
Spandidos, DA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 245 (01) :75-80
[26]  
THAKUR S, 1994, ONCOGENE, V9, P2335
[27]  
Thomas JE, 1997, CELL GROWTH DIFFER, V8, P801
[28]   DECREASED EXPRESSION OF BRCA1 ACCELERATES GROWTH AND IS OFTEN PRESENT DURING SPORADIC BREAST-CANCER PROGRESSION [J].
THOMPSON, ME ;
JENSEN, RA ;
OBERMILLER, PS ;
PAGE, DL ;
HOLT, JT .
NATURE GENETICS, 1995, 9 (04) :444-450
[29]   Differential subcellular localization, expression and biological toxicity of BRCA1 and the splice variant BRCA1-Delta 11b [J].
Wilson, CA ;
Payton, MN ;
Elliott, GS ;
Buaas, FW ;
Cajulis, EE ;
Grosshans, D ;
Ramos, L ;
Reese, DM ;
Slamon, DJ ;
Calzone, FJ .
ONCOGENE, 1997, 14 (01) :1-16
[30]   DISTINCT TRANSCRIPTION START SITES GENERATE 2 FORMS OF BRCA1 MESSENGER-RNA [J].
XU, CF ;
BROWN, MA ;
CHAMBERS, JA ;
GRIFFITHS, B ;
NICOLAI, H ;
SOLOMON, E .
HUMAN MOLECULAR GENETICS, 1995, 4 (12) :2259-2264