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大鼠红藻氨酸受体亚基KA2的基因结构及一个内含子负调控区域的特征

Gene structure of the rat kainate receptor subunit KA2 and characterization of an intronic negative regulatory region.

作者信息

Huang F, Gallo V

机构信息

Section on Molecular Neurobiology of Glia, Laboratory of Cellular and Molecular Neurophysiology, NICHD, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Biol Chem. 1997 Mar 28;272(13):8618-27. doi: 10.1074/jbc.272.13.8618.

Abstract

We have isolated and analyzed the structure of the gene grik5 (glutamate receptor ionotropic kainate 5), encoding the rat kainate receptor subunit KA2. Six overlapping DNA fragments containing the entire grik5 gene were identified in a rat genomic library. grik5 is a unique gene composed of 20 exons that together span over 54 kilobases (kb). Reporter gene analysis demonstrated that 2 kb of grik5 5'-flanking sequence confers tissue-specific expression on a chloramphenicol acetyltransferase gene in vitro. We show that (i) the first intron of grik5 (3.4 kb) inhibited transcription of the chloramphenicol acetyltransferase gene driven by the 2-kb grik5 5'-flanking region; (ii) the negative regulatory element was located within 500 bp of the 3'-end of intron 1, and this 500-bp fragment selectively bound nuclear proteins isolated from neural and nonneural cells; (iii) the effect of the negative regulatory element on grik5 transcription was orientation- and distance-independent; and (iv) a 24-nucleotide sequence (CTTTCTGTGGCCTCTGACCTTTCC) was identified as the binding site for nuclear proteins within the 500-bp fragment, as determined by footprinting and gel shift assays. We conclude that an intronic element that displays features of a silencer modulates grik5 transcription.

摘要

我们已经分离并分析了编码大鼠海人酸受体亚基KA2的基因grik5(离子型海人酸谷氨酸受体5)的结构。在大鼠基因组文库中鉴定出了六个包含整个grik5基因的重叠DNA片段。grik5是一个独特的基因,由20个外显子组成,这些外显子加起来跨越超过54千碱基(kb)。报告基因分析表明,2 kb的grik5 5'侧翼序列在体外赋予氯霉素乙酰转移酶基因组织特异性表达。我们发现:(i)grik5的第一个内含子(3.4 kb)抑制了由2-kb grik5 5'侧翼区域驱动的氯霉素乙酰转移酶基因的转录;(ii)负调控元件位于内含子1 3'末端的500 bp内,并且这个500-bp片段选择性地结合从神经细胞和非神经细胞中分离出的核蛋白;(iii)负调控元件对grik5转录的影响与方向和距离无关;(iv)通过足迹法和凝胶迁移试验确定,一个24个核苷酸的序列(CTTTCTGTGGCCTCTGACCTTTCC)被鉴定为500-bp片段内核蛋白的结合位点。我们得出结论,一个具有沉默子特征的内含子元件调节grik5的转录。

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