MOLECULAR-CLONING, GENOMIC ORGANIZATION, AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PANCREATITIS-ASSOCIATED PROTEIN (PAP) GENE

被引:57
作者
DUSETTI, NJ
FRIGERIO, JM
FOX, MF
SWALLOW, DM
DAGORN, JC
IOVANNA, JL
机构
[1] INSERM,U315,F-13009 MARSEILLE,FRANCE
[2] UNIV LONDON UNIV COLL,GALTON LAB,MRC,HUMAN BIOCHEM GENET UNIT,LONDON NW1 2HE,ENGLAND
关键词
D O I
10.1006/geno.1994.1019
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
Pancreatitis-associated protein (PAP) is a secretory pancreatic protein present in small amounts in normal pancreas and overexpressed during the acute phase of the pancreatitis. In this paper, we describe the cloning, characterization, and chromosomal mapping of the human PAP gene. The gene spans 2748 bp and contains six exons interrupted by five introns. The gene has a typical promoter containing the sequences TATAAA and CCAAT 28 and 52 bp upstream of the cap site, respectively. We found striking similarities in genomic organization as well as in the promoter sequences between the human and rat PAP genes. The human PAP gene was mapped to chromosome 2p12 using rodent-human hybrid cells and in situ chromosomal hybridization. This localization coincides with that of the reg/lithostathine gene, which encodes a pancreatic secretory protein structurally related to PAP, suggesting that both genes derived from the same ancestral gene by duplication. (C) 1994 Academic Press,Inc.
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收藏
页码:108 / 114
页数:7
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