Differential expression of uterine progesterone receptor forms A and B during the menstrual cycle

被引:97
作者
Mangal, RK
Wiehle, RD
Poindexter, AN
Weigel, NL
机构
[1] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Obstet & Gynecol, Houston, TX 77030 USA
关键词
D O I
10.1016/S0960-0760(97)00119-2
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
Recent studies suggest that the progesterone receptor isoforms (PR-A and PR-B) activate genes differentially and that PR-A may act as a repressor of PR-B function. Hence, the absolute and relative expression of the two isoforms will determine the response to progesterone. We have measured their relative expression in the uterus of cycling women who underwent endometrial biopsy. PR isoforms were identified on blots of SDS-PAGE gels by reaction with the AB-52 antibody after immunoprecipitation from endometrial extract. Both isoforms were highest in the peri-ovulatory phase, but levels of PR-A were always higher than those of PR-B. The ratio of PR-A to PR-B changed during the menstrual cycle. Between days 2 and 8, PR-B is almost undetectable and the A:B ratio is >10:1. From days 9 to 13, the ratio is about 5:1, and it is about 2:1 between days 14 and 16. Thereafter, PR-B dwindles rapidly and is virtually undetectable at the end of the cycle. In various hypoestrogenic environments, PR-B expression was reduced. However, exogenous estrogens in the follicular phase in the form of oral contraceptives, enhanced PR-B expression. These data support the possibility that progesterone acts through cycle-specific PR isoforms. (C) 1997 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:195 / 202
页数:8
相关论文
共 41 条
[1]   CYTOPLASMIC AND NUCLEAR ESTRADIOL AND PROGESTERONE RECEPTORS IN HUMAN ENDOMETRIUM [J].
BAYARD, F ;
DAMILANO, S ;
ROBEL, P ;
BAULIEU, EE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1978, 46 (04) :635-648
[2]   GENE-REGULATION BY STEROID-HORMONES [J].
BEATO, M .
CELL, 1989, 56 (03) :335-344
[3]   EFFECTS OF HORMONE AND CELLULAR MODULATORS OF PROTEIN-PHOSPHORYLATION ON TRANSCRIPTIONAL ACTIVITY, DNA-BINDING, AND PHOSPHORYLATION OF HUMAN PROGESTERONE RECEPTORS [J].
BECK, CA ;
WEIGEL, NL ;
EDWARDS, DP .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (04) :607-620
[4]  
BELL SC, 1991, HUMAN REPROD, V1, P129
[5]   SEASONAL-CHANGES IN THE MOLECULAR-SPECIES AND NUCLEAR-BINDING OF THE CHICK OVIDUCT PROGESTERONE RECEPTOR [J].
BOYD, PA ;
SPELSBERG, TC .
BIOCHEMISTRY, 1979, 18 (17) :3685-3690
[6]  
CHALBOS D, 1994, J BIOL CHEM, V269, P23007
[7]   PROGESTIN REGULATION OF CELLULAR PROLIFERATION [J].
CLARKE, CL ;
SUTHERLAND, RL .
ENDOCRINE REVIEWS, 1990, 11 (02) :266-301
[8]   THE A-FORMS AND B-FORMS OF THE CHICKEN PROGESTERONE-RECEPTOR ARISE BY ALTERNATE INITIATION OF TRANSLATION OF A UNIQUE MESSENGER-RNA [J].
CONNEELY, OM ;
MAXWELL, BL ;
TOFT, DO ;
SCHRADER, WT ;
OMALLEY, BW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 149 (02) :493-501
[9]   IMMUNOLOGICAL ANALYSIS OF HUMAN-BREAST CANCER PROGESTERONE RECEPTORS .1. IMMUNOAFFINITY PURIFICATION OF TRANSFORMED RECEPTORS AND PRODUCTION OF MONOCLONAL-ANTIBODIES [J].
ESTES, PA ;
SUBA, EJ ;
LAWLERHEAVNER, J ;
ELASHRYSTOWERS, D ;
WEI, LL ;
TOFT, DO ;
SULLIVAN, WP ;
HORWITZ, KB ;
EDWARDS, DP .
BIOCHEMISTRY, 1987, 26 (19) :6250-6262
[10]   PROGESTIN-MEDIATED CHANGES IN PROGESTERONE-RECEPTOR FORMS IN THE NORMAL HUMAN-ENDOMETRIUM [J].
FEIL, PD ;
CLARKE, CL ;
SATYASWAROOP, PG .
ENDOCRINOLOGY, 1988, 123 (05) :2506-2513