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Factors which regulate differentiation of the adrenal cortex and gonads from their common primordium.

Factors which regulate differentiation of the adrenal cortex and gonads from their common primordium.
调节肾上腺皮质和性腺从其共同原基分化的因素。
批准号:
09680730
负责人:
HATANO Osamu
金额:
$1.73万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1999

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中文摘要
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英文摘要
The previous study on expression of Ad4BP/SF-1 in rat embryos demonstrated that steroid-hormone-producing cells of adrenal cortex and gonads are derived from a common precursor named the "adreno-genital primordium". The analysis of the differentiation process of the primordium revealed that it consists of 4 steps where the interaction between steroidogenic precursor cells and primordial germ cells seems to play an important role. The aim of this research project is to address the question of the molecular mechanism that underlies the differentiation of the adreno-genital primordium to an adrenocortical and a gonadal primordia. Pre-adipocyte factor 1 (Pref-1), alternatively named ZOG, was found to be expressed in the adreno-genital primordium and continued to be expressed only in the adrenocortical primordium but not in the gonadal primordium. In the adult adrenal cortex, the expression of Pref-1 is restricted to the zona glomerulosa. From adrenal enucleation experiments, Pref-1 was suggested to function as a differentiation suppressor in the adrenocortical cells as well as in pre-adipocytes. Analyses of Pref-1 gene promoter with co-transfection assays have shown that WT1 down-regulated the transcription of Pref-1 gene. The continued expression and the down-regulation of Pref-1 gene may be essential for the formation of the adrenocortical and gonadal primordia, respectively.
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Sato, K., et al.: "Evidence for the involvment of a src-related tyrosine kinase in the Xenopus egg activation"Dev. Biol.. 209. 308-320 (1999)
Sato, K. 等人:“非洲爪蟾卵激活中 src 相关酪氨酸激酶参与的证据”Dev.
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通讯作者:
Hatano, O., et al.: "Molecular Steroidogenesis (Frontier Science series No. 29)"Universal Academy Press Inc. (Tokyo). 4 (2000)
Hatano, O.等人:“分子类固醇生成(前沿科学系列第 29 期)”Universal Academy Press Inc.(东京)。
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Harada N.,et al: "Histological Lesions in Aromatase-Deficient Mice"Molecular Steroidogenesis(Frontier Science Series No.29) Universal Academy Press Inc.(Tokyo). 29. 133-136 (2000)
Harada N.等人:“芳香酶缺陷小鼠的组织学病变”分子类固醇生成(前沿科学系列第 29 期)Universal Academy Press Inc.(东京)。
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通讯作者:
N.Harada,O.Hatano: "Aromatase Inhibitors stabilize aromatase for protein degradation in cultured human tumor cells." Brit.J.Cancer. 77. 567-572 (1998)
N.Harada、O.Hatano:“芳香酶抑制剂可稳定芳香酶,从而促进培养的人类肿瘤细胞中的蛋白质降解。”
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40
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