Requirement for DARPP-32 in progesterone-facilitated sexual receptivity in female rats and mice

被引:102
作者
Mani, SK [1 ]
Fienberg, AA
O'Callaghan, JP
Snyder, GL
Allen, PB
Dash, PK
Moore, AN
Mitchell, AJ
Bibb, J
Greengard, P
O'Malley, BW
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Rockefeller Univ, Mol & Cellular Neurosci Lab, New York, NY 10021 USA
[3] NIOSH, Ctr Dis Control & Prevent, Morgantown, WV 26505 USA
[4] Univ Texas, Sch Med, Dept Neurobiol & Anat, Houston, TX 77030 USA
关键词
D O I
10.1126/science.287.5455.1053
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
DARPP-32, a dopamine- and adenosine 3',5'-monophosphate (cAMP)-regulated phosphoprotein (32 kilodaltons in size), is an obligate intermediate in progesterone (P)-facilitated sexual receptivity in female rats and mice. The facilitative effect of P on sexual receptivity in female rats was blocked by antisense oligonucleotides to DARPP-32. Homozygous mice carrying a null mutation for the DARPP-32 gene exhibited minimal levels of P-facilitated sexual receptivity when compared to their wild-type Littermates. P significantly increased hypothalamic cAMP levels and cAMP-dependent protein kinase activity. These increases were not inhibited by a D-1 subclass dopamine receptor antagonist. P also enhanced phosphorylation of DARPP-32 on threonine 34 in the hypothalamus of mice. DARPP-32 activation is thus an obligatory step in progestin receptor regulation of sexual receptivity in rats and mice.
引用
收藏
页码:1053 / 1056
页数:4
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