Ardell M D, Makhija A K, Oliveira L, Miniou P, Viegas-Péquignot E, Pittler S J
Department of Biochemistry and Molecular Biology, College of Medicine, University of South Alabama, Mobile 36688-0002, USA.
Genomics. 1995 Jul 1;28(1):32-8. doi: 10.1006/geno.1995.1102.
A unique glutamic acid-rich protein was previously identified in bovine rod photoreceptors (Sugimoto et al., 1991, Proc. Natl. Acad. Sci. USA 88: 3116-3119) and later suggested to be a third subunit (gamma) of the rod cGMP-gated cation channel (Chen et al., 1994, Proc. Natl. Acad. Sci. USA 91: 11757-11761). Here, we report on the characterization of the GAR1 gene encoding a human homolog of bovine gamma. Sequence analysis of cDNA clones encoding human gamma revealed an open reading frame predicting a protein of 299 amino acids (approximately 32 kDa), half the size of the bovine gamma subunit. Comparison of the N-terminal half of bovine gamma with the predicted human gamma sequence revealed 90% identity within the first 31 amino acids, and only 60% homology was found throughout the remainder of the protein sequence. As in bovine gamma, the predicted isoelectric point of the human protein is very acidic despite the absence of the bovine C-terminal glutamic acid-rich domain. The integrity of the cDNA sequence was confirmed by analysis of several overlapping genomic clones that span the GAR1 gene. The protein coding region of the gene consists of 12 exons spanning approximately 11 kb with exon sequence identical to that of the cDNA clones. PCR of somatic cell hybrid DNA with primer pairs that amplify a portion of the GAR1 gene (locus designation CNCG3L) demonstrate localization to chromosome 16. The location of the gene was further delimited by fluorescence in situ hybridization placing the gene at 16q13.(ABSTRACT TRUNCATED AT 250 WORDS)
先前在牛视杆光感受器中鉴定出一种独特的富含谷氨酸的蛋白质(杉本等人,1991年,《美国国家科学院院刊》88: 3116 - 3119),后来有人提出它是视杆细胞环磷酸鸟苷门控阳离子通道的第三个亚基(γ)(陈等人,1994年,《美国国家科学院院刊》91: 11757 - 11761)。在此,我们报告了编码牛γ亚基人类同源物的GAR1基因的特征。对编码人类γ亚基的cDNA克隆进行序列分析,发现一个开放阅读框,预测编码一个299个氨基酸(约32 kDa)的蛋白质,其大小是牛γ亚基的一半。将牛γ亚基的N端一半与预测的人类γ序列进行比较,在前31个氨基酸内显示出90%的同一性,而在整个蛋白质序列的其余部分仅发现60%的同源性。与牛γ亚基一样,尽管人类蛋白质没有牛C端富含谷氨酸的结构域,但其预测的等电点非常酸性。通过分析跨越GAR1基因的几个重叠基因组克隆,证实了cDNA序列的完整性。该基因的蛋白质编码区由12个外显子组成,跨度约11 kb,外显子序列与cDNA克隆相同。用扩增GAR1基因一部分(基因座命名为CNCG3L)的引物对进行体细胞杂交DNA的PCR,证明其定位于16号染色体。通过荧光原位杂交进一步确定了该基因的位置,将其定位在16q13。(摘要截断于250字)