Molecular cloning and chromosomal localization of PD-I beta (PDNP3), a new member of the human phosphodiesterase I genes

被引:68
作者
JinHua, P
Goding, JW
Nakamura, H
Sano, K
机构
[1] KOBE UNIV,SCH MED,DEPT PEDIAT,CHUO KU,KOBE,HYOGO 650,JAPAN
[2] MONASH UNIV,ALFRED HOSP,DEPT PATHOL & IMMUNOL,MELBOURNE,VIC 3181,AUSTRALIA
关键词
D O I
10.1006/geno.1997.4949
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Phosphodiesterase I (EC 3.1.4.1)/nucleotide pyrophosphatase (EC 3.6.1.9) enzymes are a family of type II transmembrane proteins that catalyze the cleavage of phosphodiester and phosphosulfate bonds of a variety of molecules, including deoxynucleotides, NAD, and nucleotide sugars. The human genes for two members of this family have been cloned and designated PC-1 (PDNP1) and PD-I alpha/autotaxin (PDNP2). We have now cloned the third member of this family from a human prostate cDNA library and designated it human phosphodiesterase-I beta (PD-I beta). The PD-I beta cDNA contains a 2625-bp-long open reading frame which encodes an 875-amino-acid protein. COS-7 cells transfected with an expression vector, pBK-CMV, containing PD-I beta cDNA had high phosphodiesterase I activity compared to the mock-transfected cells. By using in situ hybridization to human metaphase chromosomes, we have assigned the locus for the PD-I beta (PDNP3) gene to the q22 region of human chromosome 6. (C) 1997 Academic Press.
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页码:412 / 415
页数:4
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