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源自大鼠mGluR5基因两个不同转录起始位点的mRNA可变形式的区域表达与调控。

Regional expression and regulation of alternative forms of mRNAs derived from two distinct transcription initiation sites of the rat mGluR5 gene.

作者信息

Yamaguchi S, Nakanishi S

机构信息

Department of Biological Sciences, Kyoto University Faculty of Medicine, Japan.

出版信息

J Neurochem. 1998 Jul;71(1):60-8. doi: 10.1046/j.1471-4159.1998.71010060.x.

Abstract

Metabotropic glutamate receptor (mGluR) subtype 5 is expressed in both neuronal and glial cells and is thought to play an important role in neuronal plasticity. This expression is up-regulated during the early postnatal period and is induced in cultured astrocytes by specific growth factors. To investigate the mechanism underlying the regulation of mGluR5 expression, we isolated and characterized genomic clones containing the 5'-upstream exons and their flanking regions of the mGluR5 gene. On the basis of the mGluR5 genomic structure, cDNA recloning of the 5'-extreme region of mGluR5 as well as primer extension analysis indicated that mGluR5 mRNA is generated from two alternative first exons, termed exon 1A and exon 1B, which are separated by 1,949 bp and then connected to the common exon 2. Northern blot and in situ hybridization analyses indicated that two distinct transcription initiation sites are commonly used in the expression of mGluR5 mRNA in various, but specialized, brain regions and that these two alternative forms of mGluR5 mRNA are similarly up-regulated or down-regulated during the early postnatal period, depending on the brain regions. The two mRNAs are also expressed in cultured astrocytes but respond differently to growth factor-mediated induction. This study provides the genetic basis indicating the diverse mechanisms involved in the regulation of mGluR5 expression.

摘要

代谢型谷氨酸受体(mGluR)5亚型在神经元和神经胶质细胞中均有表达,被认为在神经元可塑性中发挥重要作用。这种表达在出生后早期上调,并由特定生长因子在培养的星形胶质细胞中诱导产生。为了研究mGluR5表达调控的潜在机制,我们分离并鉴定了包含mGluR5基因5'上游外显子及其侧翼区域的基因组克隆。基于mGluR5的基因组结构,对mGluR5 5'末端区域进行cDNA重新克隆以及引物延伸分析表明,mGluR5 mRNA由两个选择性的第一外显子产生,分别称为外显子1A和外显子1B,它们相隔1949 bp,然后连接到共同的外显子2。Northern印迹和原位杂交分析表明,在不同但特定的脑区中,mGluR5 mRNA的表达通常使用两个不同的转录起始位点,并且这两种mGluR5 mRNA的替代形式在出生后早期根据脑区的不同而同样上调或下调。这两种mRNA也在培养的星形胶质细胞中表达,但对生长因子介导的诱导反应不同。本研究提供了遗传基础,表明mGluR5表达调控涉及多种机制。

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