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Cytoplasmic-nuclear trafficking of progesterone receptor. In vivo study of the mechanism of action of antiprogestins.

作者信息

Guiochon-Mantel A, Delabre K, Lescop P, Perrot-Applanat M, Milgrom E

机构信息

Unité de Recherche Inserm 135, Faculté de Médecine Paris-Sud, Le Kremlin Bicetre, France.

出版信息

Biochem Pharmacol. 1994 Jan 13;47(1):21-4. doi: 10.1016/0006-2952(94)90433-2.

DOI:10.1016/0006-2952(94)90433-2
PMID:8311841
Abstract

The signal responsible for the nuclear localization of the progesterone receptor has been characterized. The study of the mechanism of this nuclear localization has revealed that the receptor continuously shuttles between the nucleus and the cytoplasm. The receptor diffuses into the cytoplasm and is constantly and actively transported back into the nucleus. Preliminary evidence suggests that the same mechanism exists for estradiol and glucocorticoid receptors. Experiments designed to study the traffic of steroid hormone receptors have been applied to the determination of the molecular mechanism of action of antisteroids. Using these techniques, we have shown that two major antiprogestins, RU486 and ZK98299, act at the same point in the cell as the hormone.

摘要

相似文献

1
Cytoplasmic-nuclear trafficking of progesterone receptor. In vivo study of the mechanism of action of antiprogestins.
Biochem Pharmacol. 1994 Jan 13;47(1):21-4. doi: 10.1016/0006-2952(94)90433-2.
2
The Ernst Schering Poster Award. Intracellular traffic of steroid hormone receptors.
J Steroid Biochem Mol Biol. 1996 Jan;56(1-6 Spec No):3-9. doi: 10.1016/0960-0760(95)00268-5.
3
Mechanisms of nuclear localization of the progesterone receptor.孕酮受体的核定位机制。
J Steroid Biochem Mol Biol. 1992 Mar;41(3-8):209-15. doi: 10.1016/0960-0760(92)90346-k.
4
The antiprogestins RU486 and ZK98299 affect follicle-stimulating hormone secretion differentially on estrus, but not on proestrus.抗孕激素RU486和ZK98299对发情期促卵泡激素分泌的影响不同,但对发情前期没有影响。
Endocrinology. 1997 Jun;138(6):2286-90. doi: 10.1210/endo.138.6.5161.
5
Antiprogestins suppress basal and activin-stimulated follicle-stimulating hormone secretion in an estrogen-dependent manner.抗孕激素以雌激素依赖的方式抑制基础和激活素刺激的促卵泡激素分泌。
Endocrinology. 1998 May;139(5):2223-8. doi: 10.1210/endo.139.5.6015.
6
The antagonists RU486 and ZK98299 stimulate progesterone receptor binding to deoxyribonucleic acid in vitro and in vivo, but have distinct effects on receptor conformation.拮抗剂RU486和ZK98299在体外和体内均能刺激孕酮受体与脱氧核糖核酸结合,但对受体构象有不同影响。
Endocrinology. 1998 Apr;139(4):1905-19. doi: 10.1210/endo.139.4.5944.
7
Two types of antiprogestins identified by their differential action in transcriptionally active extracts from T47D cells.通过它们在T47D细胞转录活性提取物中的差异作用鉴定出两种抗孕激素。
Nucleic Acids Res. 1991 Mar 25;19(6):1227-34. doi: 10.1093/nar/19.6.1227.
8
Two types of anti-progestins have distinct effects on site-specific phosphorylation of human progesterone receptor.两种抗孕激素对人孕激素受体的位点特异性磷酸化具有不同的作用。
J Biol Chem. 1996 Jan 12;271(2):1209-17. doi: 10.1074/jbc.271.2.1209.
9
Antiprogestins prevent progesterone receptor binding to hormone responsive elements in vivo.抗孕激素在体内可阻止孕激素受体与激素反应元件结合。
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11333-7. doi: 10.1073/pnas.91.24.11333.
10
ZK98299, a novel antiprogesterone that does not interact with chicken oviduct progesterone receptor.ZK98299,一种新型抗孕激素,不与鸡输卵管孕激素受体相互作用。
Biochim Biophys Acta. 1991 Sep 3;1094(2):185-92. doi: 10.1016/0167-4889(91)90007-k.

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