Genomic organization, chromosomal localization, and alternative splicing of the human phosphodiesterase 8B gene

被引:37
作者
Hayashi, M [1 ]
Shimada, Y [1 ]
Nishimura, Y [1 ]
Hama, T [1 ]
Tanaka, T [1 ]
机构
[1] Mie Univ, Sch Med, Dept Mol & Cellular Pharmacol, Tsu, Mie 5148507, Japan
基金
日本学术振兴会;
关键词
D O I
10.1016/S0006-291X(02)02371-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have characterized the gene for human phosphodiesterase 8B, PDE8B, and cloned the full-length cDNA for human PDE8B (PDE8B1) and two splice variants (PDE8B2 and PDE8B3). The PDE8B gene is mapped to the long arm of chromosome 5 (5q13) and is composed of 22 exons spanning over similar to200 kb. The donor and acceptor splice site sequences match the consensus sequences for the exon-intron boundaries of most eukaryotic genes. PDE8B1 encodes an 885 amino acid enzyme, containing an N-terminal REC domain, a PAS domain, and a C-terminal catalytic domain. PDE8B2 and PDE8B3 both have deletion in the PAS domain and encode 838 and 788 amino acid proteins, respectively. RT-PCR analysis revealed that while PDE8B1 is the most abundant variant in thyroid gland, PDE8B3, but not PDE8B1, is the most abundant form in brain. These findings suggest that selective usage of exons produces three different PDE8B variants that exhibit a tissue-specific expression pattern. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1253 / 1258
页数:6
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