Identification of ERF-1 as a member of the AP2 transcription factor family

被引:129
作者
McPherson, LA [1 ]
Baichwal, VR [1 ]
Weigel, RJ [1 ]
机构
[1] TULARIK INC, S SAN FRANCISCO, CA 94080 USA
关键词
estrogen receptor; breast cancer; promoter; gene; RNA;
D O I
10.1073/pnas.94.9.4342
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ERF-1 transcription factor was previously shown to be involved in the regulation of estrogen receptor (ER) gene transcription in hormonally responsive breast and endometrial carcinomas. In this study we sought to identify the gene for ERF-1, ERF-1 activates ER gene transcription by binding to the imperfect palindrome CCCT-GCGGGG within the promoter of the ER gene. ERF-1 protein was purified from the ER-positive breast carcinoma cell line, MCF7, utilizing ion exchange and DNA affinity chromatography. Peptide sequence analysis was used to isolate a 2,7 kb cDNA clone from an MCF7 cDNA library. This cDNA encodes a protein of 48 kDa previously identified as the AP2 gamma transcription factor. By gel-shift analysis, in vitro synthesized ERF-1 comigrates with MCF7 native ERF-1 complex and demonstrates identical sequence binding specificity as native ERF-1. In addition, AP2 polyclonal antisera supershifts both in vitro synthesized and native ERF-1 complexes. These results show that ERF-1 is a member of the AP2 family of developmentally regulated transcription factors. Given the central role of ER expression in breast carcinoma biology. ERF-1 is likely to regulate expression of a set of genes characteristic of the hormonally-responsive breast cancer phenotype.
引用
收藏
页码:4342 / 4347
页数:6
相关论文
共 27 条
[1]   CHARACTERIZATION OF THE AUTOANTIGEN-LA AS A NUCLEIC-ACID DEPENDENT ATPASE DATPASE WITH MELTING PROPERTIES [J].
BACHMANN, M ;
PFEIFER, K ;
SCHRODER, HC ;
MULLER, WEG .
CELL, 1990, 60 (01) :85-93
[2]  
BALLARD D W, 1989, New Biologist, V1, P83
[3]   THE DEVELOPMENTALLY-REGULATED TRANSCRIPTION FACTOR AP-2 IS INVOLVED IN C-ERBB-2 OVEREXPRESSION IN HUMAN MAMMARY-CARCINOMA [J].
BOSHER, JM ;
WILLIAMS, T ;
HURST, HC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :744-747
[4]  
CARMECI C, 1997, IN PRESS AM J PATHOL
[5]   IN-VIVO FUNCTIONAL-ANALYSIS OF THE MOUSE ESTROGEN-RECEPTOR GENE PROMOTER - A TRANSGENIC MOUSE MODEL TO STUDY TISSUE-SPECIFIC AND DEVELOPMENTAL REGULATION OF ESTROGEN-RECEPTOR GENE-TRANSCRIPTION [J].
CICATIELLO, L ;
COBELLIS, G ;
ADDEO, R ;
PAPA, M ;
ALTUCCI, L ;
SICA, V ;
BRESCIANI, F ;
LEMEUR, M ;
KUMAR, VL ;
CHAMBON, P ;
WEISZ, A .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (08) :1077-1090
[6]  
DECONINCK EC, 1995, MOL CELL BIOL, V15, P2191
[7]  
DIGHAM JD, 1983, NUCLEIC ACIDS RES, V11, P1475
[8]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989
[9]   ESTROGEN-RECEPTOR MUTATIONS IN BREAST-CANCER [J].
FUQUA, SAW ;
CHAMNESS, GC ;
MCGUIRE, WL .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, 51 (02) :135-139
[10]  
HELLMAN U, 1995, ANAL BIOCHEM, V191, P332