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大鼠酪氨酸羟化酶基因的DNA调控序列在导致侏儒表型的转基因小鼠中枢神经系统中,指导人生长激素报告基因产生正确的儿茶酚胺能细胞类型特异性。

DNA regulatory sequences of the rat tyrosine hydroxylase gene direct correct catecholaminergic cell-type specificity of a human growth hormone reporter in the CNS of transgenic mice causing a dwarf phenotype.

作者信息

Banerjee S A, Roffler-Tarlov S, Szabo M, Frohman L, Chikaraishi D M

机构信息

Department of Microbiology, Tufts University School of Medicine, Boston, MA 02111.

出版信息

Brain Res Mol Brain Res. 1994 Jul;24(1-4):89-106. doi: 10.1016/0169-328x(94)90121-x.

Abstract

Transgenic mice bearing 4.8 kilobases (kb) of upstream rat tyrosine hydroxylase (TH) sequences linked to a human growth hormone gene (hGH) exhibited cell-specific expression of hGH in all the appropriate catecholaminergic neurons in the central nervous system (CNS), although with different penetrance in two different mouse lineages. No ectopic expression was observed in any brain or peripheral region in one founder and its progeny. In another founder there was some ectopic expression in addition to appropriate and high levels of tissue-specific expression in all catecholaminergic areas. These results identify regulatory sequences that are sufficient for targeting expression to all catecholaminergic CNS neurons. Also, expression of exogenous hGH in the hypothalamus caused a dwarf phenotype, generating a novel genetic model for GH deficiency of hypothalamic origin.

摘要

携带与人类生长激素基因(hGH)相连的4.8千碱基(kb)大鼠酪氨酸羟化酶(TH)上游序列的转基因小鼠,在中枢神经系统(CNS)所有合适的儿茶酚胺能神经元中表现出hGH的细胞特异性表达,尽管在两个不同的小鼠品系中有不同的外显率。在一个奠基者及其后代的任何脑区或外周区域均未观察到异位表达。在另一个奠基者中,除了在所有儿茶酚胺能区域有适当且高水平的组织特异性表达外,还存在一些异位表达。这些结果确定了足以将表达靶向所有中枢神经系统儿茶酚胺能神经元的调控序列。此外,下丘脑中外源hGH的表达导致了侏儒表型,产生了一种新的下丘脑源性生长激素缺乏的遗传模型。

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