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一种与膜相关的孕酮结合蛋白,即25-Dx,在参与雌性生殖行为的脑区中受孕酮调节。

A membrane-associated progesterone-binding protein, 25-Dx, is regulated by progesterone in brain regions involved in female reproductive behaviors.

作者信息

Krebs C J, Jarvis E D, Chan J, Lydon J P, Ogawa S, Pfaff D W

机构信息

Laboratory of Neurobiology and Behavior and Laboratory of Animal Behavior, The Rockefeller University, New York, NY 10021, USA.

出版信息

Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12816-21. doi: 10.1073/pnas.97.23.12816.

Abstract

The ventromedial hypothalamus (VMH) plays a central role in the regulation of the female reproductive behavior lordosis, a behavior dependent upon the sequential activation of receptors for the ovarian steroid hormones estradiol (E) and progesterone (P). These receptors function as transcription factors to alter the expression of target genes. To discover behaviorally relevant genes targeted by E and P in the VMH, we used the differential display PCR to identify messenger RNAs that are differentially expressed in the hypothalamus of ovariectomized (ovx) rats treated with E alone compared with ovariectomized rats treated with E and P. We show here that one interesting mRNA within the hypothalamus that is repressed by P after E priming encodes the protein 25-Dx, the rat homolog of the human membrane-associated P-binding protein Hpr6.6. Neurons in the brain containing the highest levels of 25-Dx are located in several nuclei of the basal forebrain, including the VMH. 25-Dx expression is also higher in the hypothalamus of female P receptor "knockout" mice than in their wild-type littermates. These findings suggest a mechanism in which the activation of nuclear P receptor represses expression of a membrane P receptor, 25-Dx, during lordosis facilitation.

摘要

腹内侧下丘脑(VMH)在雌性生殖行为——脊柱前凸的调节中起核心作用,这种行为依赖于卵巢甾体激素雌二醇(E)和孕酮(P)受体的顺序激活。这些受体作为转录因子来改变靶基因的表达。为了发现VMH中被E和P靶向的与行为相关的基因,我们使用差异显示PCR来鉴定在仅用E处理的去卵巢(ovx)大鼠下丘脑与用E和P处理的去卵巢大鼠下丘脑相比差异表达的信使RNA。我们在此表明,下丘脑内一种有趣的mRNA在E预处理后被P抑制,其编码蛋白质25-Dx,即人类膜相关P结合蛋白Hpr6.6的大鼠同源物。大脑中25-Dx水平最高的神经元位于基底前脑的几个核中,包括VMH。在雌性P受体“敲除”小鼠的下丘脑中,25-Dx的表达也高于其野生型同窝小鼠。这些发现提示了一种机制,即在促进脊柱前凸过程中,核P受体激活会抑制膜P受体25-Dx的表达。

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