Regulation of cAMP responsive element binding modulator isoforms in cultured rat ovarian granulosa cells

被引:16
作者
Kameda, T
Mizutani, T
Minegishi, T
Ibuki, Y
Miyamoto, K [1 ]
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Biosignal Res Ctr, Gunma 3718512, Japan
[2] Gunma Univ, Sch Med, Dept Obstet & Gynecol, Gunma 3718511, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 1999年 / 1445卷 / 01期
关键词
granulosa cell; FSH inducible gene; gene expression; cAMP responsive element binding modulator; inducible cAMP early repressor; subtraction cloning;
D O I
10.1016/S0167-4781(99)00018-4
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
A pituitary glycoprotein hormone FSH stimulates ovarian granulosa cells to induce ovarian follicular development. In this study we identified rat ovarian genes that were rapidly induced by FSH in the cultured rat granulosa cells by means of subtraction cloning. Complementary DNA clones encoding cAMP responsive element binding modulator (CREM) were identified as one of the FSH inducible genes. Northern blotting and reverse transcription and polymerase chain reaction (RT-PCR) analyses revealed that only the repressor type of CREM gene products, ICER (inducible cAMP early repressor) isoforms, were induced by FSH treatment in cultured rat granulosa cells. The induction of ICER by FSH was mimicked by reagents known to increase intracellular cAMP levels, indicating that the induction is through cAMP and protein kinase A signal transduction system. Induction of ICER was also confirmed as the protein levels. Electrophoretic mobility shift assay of granulosa cell extracts with a radiolabeled double stranded oligonucleotide corresponding to somatostatin cAMP responsive element also revealed that only the ICER proteins were induced by FSH treatment, whereas levels of CREM proteins were nearly constant regardless of the FSH treatment. Our present study demonstrates that FSH-induced and cAMP-mediated induction and attenuation of transcriptional responses by CREM gene products may be a key mechanistic component for the granulosa cell differentiation and proliferation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:31 / 38
页数:8
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