CHARACTERIZATION OF THE ALDOSE REDUCTASE-ENCODING GENE FAMILY IN RAT

被引:33
|
作者
GRAHAM, C
SZPIRER, C
LEVAN, G
CARPER, D
机构
[1] NEI,BLDG 6,RM 232,9000 ROCKVILLE PIKE,BETHESDA,MD 20892
[2] UNIV LIBRE BRUXELLES,DEPT BIOL MOLEC,B-1640 RHODE ST GENESE,BELGIUM
[3] GOTHENBURG UNIV,DEPT GENET,S-40033 GOTHENBURG,SWEDEN
关键词
RECOMBINANT DNA; SEQUENCING; PSEUDOGENES; RNASE PROTECTION; CHROMOSOME LOCALIZATION; DIABETIC COMPLICATIONS; POLYOL PATHWAY;
D O I
10.1016/0378-1119(91)90326-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although the enzyme aldose reductase (AR) is implicated in the development of tissue pathology in diabetes, the exact mechanism of this involvement remains unclear. To better understand the role that expression of the aldose reductase-encoding gene (ALR) may play in diabetic complications, we have begun to analyze the gene and its regulatory regions, and we present here the sequence of four ALR genes in the rat. The putative functional gene is 14.1 kb long, has ten exons which show perfect sequence identity to the rat lens AR RNA sequence, and nine introns with classical splice-site consensus sequences. Potential regulatory elements in the 5'-flanking region of this gene include a TATA box and two CCAAT boxes. Probing rat genomic Southern blots with a fragment from the first intron indicates that there is probably only one copy of this gene in the rat genome. The other three genes are processed pseudogenes which show approx. 90% identity to the rat lens AR RNA sequence, contain no introns, and have poly(A) regions at their 3' ends. Chromosomal localization studies show the presence of ALR genes on chromosomes 3, 4 and 6 in the rat with the putative functional gene mapped on chromosome 4.
引用
收藏
页码:259 / 267
页数:9
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