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斑胸草雀雌激素受体cDNA:克隆与mRNA表达

Zebra finch estrogen receptor cDNA: cloning and mRNA expression.

作者信息

Jacobs E C, Arnold A P, Campagnoni A T

机构信息

Program in Neuroscience, UCLA, Los Angeles, CA 90095, USA.

出版信息

J Steroid Biochem Mol Biol. 1996 Oct;59(2):135-45. doi: 10.1016/s0960-0760(96)00096-9.

Abstract

In zebra finches, estrogen is a potent hormone that masculinizes the neural circuitry controlling song during development and activates song in adulthood. However, previous studies have reported conflicting patterns of estrogen receptor (ER) expression in the song control regions. To obtain additional information about the distribution of ER in the zebra finch brain, a cDNA encoding an estrogen receptor was isolated from a zebra finch hypothalamic-preoptic area cDNA library. The 2792 bp insert contains a 1764 bp open reading frame with 5' and 3' untranslated regions of 132 bp and 896 bp, respectively. The deduced polypeptide is 589 amino acids in length and is highly homologous to the estrogen receptors of chicken (97%), rat (79%), mouse (79%), human (78%), Xenopus laevis (76%) and trout (49%). Northern blot analysis revealed three ER mRNAs expressed differentially in ovary, oviduct and telencephalon. The smallest transcript, 4.1 kb, was expressed in all three tissues, whereas larger mRNAs were expressed in ovary (7.6 kb) and oviduct (8.1 kb). In situ hybridization histochemistry revealed strong labelling in the infundibular region of the hypothalamus, preoptic area, and medial caudal neostriatum. Few or no labelled cells were found in the song control nuclei (HVC, RA, MAN or Area X). These results are consistent with previous studies that have shown ER protein and binding in hypothalamic and preoptic area and a lack of ER in most regions that control song production.

摘要

在斑胸草雀中,雌激素是一种强效激素,在发育过程中使控制鸣叫的神经回路雄性化,并在成年期激活鸣叫。然而,先前的研究报告了雌激素受体(ER)在鸣叫控制区域的表达模式相互矛盾。为了获得关于ER在斑胸草雀大脑中分布的更多信息,从斑胸草雀下丘脑 - 视前区cDNA文库中分离出编码雌激素受体的cDNA。2792 bp的插入片段包含一个1764 bp的开放阅读框,其5'和3'非翻译区分别为132 bp和896 bp。推导的多肽长度为589个氨基酸,与鸡(97%)、大鼠(79%)、小鼠(79%)、人类(78%)、非洲爪蟾(76%)和鳟鱼(49%)的雌激素受体高度同源。Northern印迹分析显示三种ER mRNA在卵巢、输卵管和端脑中差异表达。最小的转录本4.1 kb在所有三种组织中表达,而较大的mRNA在卵巢(7.6 kb)和输卵管(8.1 kb)中表达。原位杂交组织化学显示在下丘脑的漏斗区、视前区和内侧尾侧新纹状体中有强烈的标记。在鸣叫控制核(HVC、RA、MAN或X区)中发现很少或没有标记细胞。这些结果与先前的研究一致,先前的研究表明ER蛋白在下丘脑和视前区有结合,而在大多数控制鸣叫产生的区域缺乏ER。

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