Genomic organization and chromosomal localization of the Asna1 gene, a mouse homologue of a bacterial arsenic-translocating ATPase gene

被引:14
作者
Bhattacharjee, H [1 ]
Ho, YS [1 ]
Rosen, BP [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Biochem & Mol Biol, Detroit, MI 48201 USA
关键词
arsenite; fluorescence in situ hybridization; rapid amplification of cDNA ends; RNA ligase mediated rapid amplification of cDNA ends; resistance;
D O I
10.1016/S0378-1119(01)00522-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The plasmid encoded ArsA ATPase in Escherichia coli is the catalytic component of an oxyanion pump that is responsible for resistance to arsenicals and antimonials. Arsenite or antimonite allosterically activates the ArsA ATPase activity. In this paper, we report the cloning and characterization of the mouse homologue (Asna1) of the bacterial arsA gene. The Asna1 gene encodes an open reading frame of 348 amino acids and exhibits 27% identity to the bacterial ArsA protein and 99% similarity to its human counterpart (hASNA-1). The Asna1 mRNA is a similar to1.3 kb transcript and is present at high levels in kidney and testis, moderate levels in brain, liver, lung and skin, and low levels in heart, small intestine, spleen, stomach, and thymus. A negligible amount of Asna1 transcript is detected in skeletal muscle. We have also characterized the genomic structure of the Asna1 gene. The gene spans over 7 kb and consists of seven exons and six introns. All splice sites conform to the GT-AG rule, except for the splice donor site of intron 4 that is GC instead of GT. Fluorescence in situ hybridization indicates that the Asna1 gene is localized in the C3-D1 region of mouse chromosome 8. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:291 / 299
页数:9
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