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Rat osteotesticular phosphatase gene (Esp): genomic structure and chromosome location.

作者信息

Lathrop W, Jordan J, Eustice D, Chen D

机构信息

Bayer Research Center, Pharmaceutical Division, Bayer Corporation, 400 Morgan Lane, West Haven, Connecticut 06516-4175, USA.

出版信息

Mamm Genome. 1999 Apr;10(4):366-70. doi: 10.1007/s003359901003.

DOI:10.1007/s003359901003
PMID:10087294
Abstract

Osteotesticular phosphatase (OST-PTPase) is a class III receptor-type tyrosine phosphatase (RPTPase). It has 10 tandem fibronectin III-like (FN-III) repeats in the extracellular region and two phosphatase domains in the intracellular region. The expression of the rat OST-PTPase gene, Esp, is restricted to osteoblasts and Sertoli cells, and the transcript level in osteoblasts is highly up-regulated by parathyroid hormone and cAMP treatment. We report here the cloning and characterization of the rat Esp gene, including a 2.9-kb 5' flanking region sequence. Two potential binding sites for Osf2/Cbfa1, an osteoblast-specific transcription factor, are present in the promoter. Esp is composed of 35 exons, but spans merely 20 kb, making it the most compact RPTPase gene identified. Each FN-III repeat is encoded by a single exon flanked with phase 1 introns. Two phosphatase domains are encoded by 16 exons in a genomic organization similar to those in RPRPalpha, RPTPgamma, and Ptprc genes. Esp was mapped by fluorescence in situ hybridization to rat chromosome 13q1. These results represent the first genomic structure of a mammalian class III RPTPase gene.

摘要

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