Regulation of RGS mRNAs by cAMP in PC12 cells

被引:70
|
作者
Pepperl, DJ
Shah-Basu, S
VanLeeuwen, D
Granneman, JG
MacKenzie, RG
机构
[1] Parke Davis Pharmaceut Res, Ann Arbor, MI 48105 USA
[2] Wayne State Univ, Dept Psychiat & Behav Neurosci, Detroit, MI 48201 USA
关键词
D O I
10.1006/bbrc.1997.8056
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
The RGS (regulators of G;protein signaling) proteins represent a novel family of proteins which attenuate G; protein mediated signaling. Using antisense ribo-probes selective for rat RGS4, RGS7, and RGS2, we examined the regulation of these RGS mRNAs in PC12 cells in response to agents which elevate intracellular cAMP. Treatment of the PC12 cells with forskolin, dibutryl cAMP, or 8-CPT-cAMP for three hours decreased RGS4 message by nearly 50%. Actinomycin D, a potent inhibitor of transcription, did not affect the forskolin-induced decrease in RGS4 message, suggesting that forskolin does not alter RGS4 message half-life. RGS7 message is also present in these cells, but was-not affected by forskolin. In contrast, RGS2 message is not evident in unstimulated cells but is strongly induced by one hour of treatment with forskolin. Taken together, these data suggest that mRNA levels of different RGS family members respond in an idiosynchratic fashion to cAMP challenge. (C) 1998 Academic Press.
引用
收藏
页码:52 / 55
页数:4
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