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通过促性腺激素释放激素(GnRH)基因特定转录调控元件在体内实现神经元特异性表达。

Neuron-specific expression in vivo by defined transcription regulatory elements of the GnRH gene.

作者信息

Lawson Mark A, Macconell Leigh A, Kim Jinah, Powl Brian T, Nelson Shelley B, Mellon Pamela L

机构信息

Department of Reproductive Medicine and Center for the Study of Reproductive Biology and Disease, University of California-San Diego, La Jolla, California 92093-0674, USA.

出版信息

Endocrinology. 2002 Apr;143(4):1404-12. doi: 10.1210/endo.143.4.8751.

DOI:10.1210/endo.143.4.8751
PMID:11897697
Abstract

The GnRH-expressing neurons are the ultimate regulator of reproductive function. GnRH gene expression is limited to this small population of neurons in the hypothalamus. Transfections using 3 kb of the rat or mouse 5'-regulatory region provide specific gene expression in the hypothalamic cell line GT1-7. The combination of two elements, a 300-bp enhancer and a 173-bp promoter, recapitulates specificity in GT1-7 cells. It was not known whether these elements could specifically target gene expression throughout development in the whole animal. We demonstrate that the 3-kb rat GnRH regulatory region provides a higher degree of specificity than the equivalent mouse sequence in a mouse hypothalamic cell line. Moreover, combination of the enhancer and the promoter of the rat gene targets expression to GnRH neurons in transgenic mice in a developmentally appropriate manner. Transgene expression is regulated by activin A, a known activator of GnRH gene expression. In contrast, the enhancer on a heterologous promoter produces inappropriate expression in vivo. We conclude that the enhancer and promoter regions of the rat GnRH gene are necessary for targeted expression to hypothalamic neurons and are sufficient to confer regulated, cell type-specific expression to a reporter gene in vivo.

摘要

表达促性腺激素释放激素(GnRH)的神经元是生殖功能的最终调节者。GnRH基因表达仅限于下丘脑的这一小群神经元。使用大鼠或小鼠3 kb的5'调控区域进行转染可在下丘脑细胞系GT1-7中实现特异性基因表达。一个300 bp的增强子和一个173 bp的启动子这两个元件的组合,在GT1-7细胞中重现了特异性。尚不清楚这些元件在整个动物的发育过程中是否能特异性地靶向基因表达。我们证明,在小鼠下丘脑细胞系中,3 kb的大鼠GnRH调控区域比等效的小鼠序列具有更高的特异性。此外,大鼠基因的增强子和启动子的组合以发育适宜的方式将转基因表达靶向转基因小鼠中的GnRH神经元。转基因表达受激活素A调控,激活素A是已知的GnRH基因表达激活剂。相反,异源启动子上的增强子在体内产生不适当的表达。我们得出结论,大鼠GnRH基因的增强子和启动子区域对于靶向表达至下丘脑神经元是必需的,并且足以在体内赋予报告基因受调控的、细胞类型特异性的表达。

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