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新型蛋白酪氨酸磷酸酶HPTP η的分子克隆、特性分析及染色体定位

Molecular cloning, characterization, and chromosomal localization of a novel protein-tyrosine phosphatase, HPTP eta.

作者信息

Honda H, Inazawa J, Nishida J, Yazaki Y, Hirai H

机构信息

Department of Molecular Biology, Jichi Medical School, Tochigi-ken, Japan.

出版信息

Blood. 1994 Dec 15;84(12):4186-94.

PMID:7994032
Abstract

Protein-tyrosine phosphatases (PTPases) are considered to play an important role in signal transduction. We previously identified partial sequences of three novel PTPases in a human leukemic cell line. F-36P. We describe here cloning, characterization, and chromosomal localization of one of the newly identified PTPases, termed as HPTP eta (human protein-tyrosine phosphatase eta). The deduced amino acid sequence was composed of an extracellular region homologous to fibronectin type III repeats, a transmembrane region, and a cytoplasmic region containing a single PTPase-like domain. Based on its primary structure, this clone belongs to type-III receptor-type PTPases. The PTPase-like domain showed PTPase activity when expressed in Escherichia coli. Antibody against the extracellular region detected a protein of 220 to 250 kD in human hematopoietic cell lines expressing HPTP eta mRNA. The antibody also recognized a protein of approximately the same molecular weight in COS cells transfected with HPTP eta cDNA, indicating that the antibody specifically recognized HPTP eta gene product and that the cloned cDNA contained full-length coding region. The chromosomal localization determined by fluorescence in situ hybridization showed that the HPTP eta gene was located at chromosome 11p11.2 on the short arm of chromosome 11, which is frequently lost or deleted in human carcinomas.

摘要

蛋白酪氨酸磷酸酶(PTPases)被认为在信号转导中起重要作用。我们之前在人白血病细胞系F-36P中鉴定出三种新型PTPases的部分序列。我们在此描述新鉴定的一种PTPase(称为HPTP eta,即人蛋白酪氨酸磷酸酶eta)的克隆、特性及染色体定位。推导的氨基酸序列由与纤连蛋白III型重复序列同源的细胞外区域、一个跨膜区域以及一个包含单个PTPase样结构域的胞质区域组成。基于其一级结构,该克隆属于III型受体型PTPases。当在大肠杆菌中表达时,PTPase样结构域显示出PTPase活性。针对细胞外区域的抗体在表达HPTP eta mRNA的人造血细胞系中检测到一种220至250 kD的蛋白质。该抗体在转染了HPTP eta cDNA的COS细胞中也识别出一种分子量大致相同的蛋白质,这表明该抗体能特异性识别HPTP eta基因产物,且克隆的cDNA包含全长编码区。通过荧光原位杂交确定的染色体定位显示,HPTP eta基因位于11号染色体短臂的11p11.2,该区域在人类癌症中经常缺失。

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