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果蝇多巴脱羧酶基因在神经元和神经胶质细胞中的调控

Regulation of the Drosophila dopa decarboxylase gene in neuronal and glial cells.

作者信息

Beall C J, Hirsh J

机构信息

Department of Biological Chemistry, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Genes Dev. 1987 Jul;1(5):510-20. doi: 10.1101/gad.1.5.510.

Abstract

A cis-regulatory element selectively required for the Drosophila melanogaster dopa decarboxylase gene (Ddc) in the central nervous system has been identified previously (Scholnick et al. 1986). Here, we show that at least one additional regulatory element is required for normal neuronal expression of Ddc. We find that Ddc is normally expressed in about 125 discrete neurons and in a diffused network comprising a subset of glial cells. The expression of in vitro-altered Ddc genes was studied by immunohistochemistry following germ line reintegration with P-element vectors. Normal neuron-specific Ddc gene expression requires both the initially identified element (element I) which is 60 bp upstream from the RNA start site, and an additional regulatory element located 800-2200 bp upstream. This latter element is required for neuronal expression but is not necessary for glial expression of Ddc. We provide a model to explain how interactions between multiple regulatory elements may serve to specify cell-specific gene expression.

摘要

先前已鉴定出果蝇黑腹果蝇多巴脱羧酶基因(Ddc)在中枢神经系统中选择性需要的一个顺式调控元件(Scholnick等人,1986年)。在此,我们表明Ddc的正常神经元表达至少还需要一个额外的调控元件。我们发现Ddc通常在约125个离散神经元以及由一部分神经胶质细胞组成的弥散网络中表达。通过用P元素载体进行种系重新整合后,采用免疫组织化学方法研究了体外改变的Ddc基因的表达。正常的神经元特异性Ddc基因表达既需要最初鉴定出的位于RNA起始位点上游60 bp处的元件(元件I),也需要位于上游800 - 2200 bp处的一个额外调控元件。后一个元件对于神经元表达是必需的,但对于Ddc的神经胶质细胞表达并非必需。我们提供了一个模型来解释多个调控元件之间的相互作用如何可能用于指定细胞特异性基因表达。

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