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人类视锥转导蛋白α亚基(GNAT2)编码基因的特性分析。

Characterization of the gene encoding human cone transducin alpha-subunit (GNAT2).

作者信息

Morris T A, Fong S L

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.

出版信息

Genomics. 1993 Aug;17(2):442-8. doi: 10.1006/geno.1993.1345.

Abstract

The human cone transducin alpha-subunit (GNAT2) gene has been completely characterized. The human GNAT2 transcription unit is 9967-bp in length and consists of eight exons with seven introns. The eight exons are identical to the reported cDNA sequence (Lerea et al., 1989). Northern blot analysis of RNA from human retinas and a retinoblastoma cell line, WERI-RB1, reveals a 1.7-kb transcript for GNAT2. Multiple transcription initiation sites were mapped for human retina and WERI-RB1 RNA by primer extension and S1 nuclease protection assays. This gene has seven initiation sites spanning 31 bp. The sequence upstream of the GNAT2 gene shows a TATA box consensus sequence at -29, a CCAAT box consensus sequence at -58 (reverse orientation), and a sequence (CCATAT) similar to the CCAAT box consensus at -76. The GNAT2 upstream sequence shows no significant identity with the upstream region of the human rod transducin alpha-subunit gene (GNAT1) or with the upstream regions of the color visual pigment genes, indicating that the expression of GNAT2 may be regulated differently than these other rod- and cone-specific proteins.

摘要

人类视锥转导蛋白α亚基(GNAT2)基因已被完全鉴定。人类GNAT2转录单元长度为9967个碱基对,由八个外显子和七个内含子组成。这八个外显子与已报道的cDNA序列(Lerea等人,1989年)相同。对来自人类视网膜和视网膜母细胞瘤细胞系WERI-RB1的RNA进行Northern印迹分析,发现GNAT2有一个1.7kb的转录本。通过引物延伸和S1核酸酶保护试验,对人类视网膜和WERI-RB1 RNA的多个转录起始位点进行了定位。该基因有七个起始位点,跨度为31个碱基对。GNAT2基因上游序列在-29处显示一个TATA盒共有序列,在-58处显示一个CCAAT盒共有序列(反向),在-76处显示一个与CCAAT盒共有序列相似的序列(CCATAT)。GNAT2上游序列与人类视杆转导蛋白α亚基基因(GNAT1)的上游区域或颜色视觉色素基因的上游区域没有明显的同源性,这表明GNAT2的表达调控方式可能与这些其他视杆和视锥特异性蛋白不同。

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