CLONING AND SEQUENCE-ANALYSIS OF CDNA CLONES FOR BOVINE AORTIC-ENDOTHELIAL-CELL TRANSGLUTAMINASE

被引：53

作者：

NAKANISHI, K ^{[1
]}

NARA, K ^{[1
]}

HAGIWARA, H ^{[1
]}

AOYAMA, Y ^{[1
]}

UENO, H ^{[1
]}

HIROSE, S ^{[1
]}

机构：

[1] TOKYO INST TECHNOL,DEPT BIOL SCI,MEGURO KU,TOKYO 152,JAPAN

来源：

EUROPEAN JOURNAL OF BIOCHEMISTRY | 1991年 / 202卷 / 01期

关键词：

D O I：

10.1111/j.1432-1033.1991.tb16338.x

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：

A cDNA clone encoding transglutaminase was isolated from a bovine-endothelial-cell cDNA library using oligonucleotide probes designed based on partial amino acid sequences of the purified protein. Sequencing of the cDNA insert revealed an open reading frame of 2061 bp coding for a protein of 687 amino acids. The sequence of bovine endothelial-cell transglutaminase was 88, 82, 80, 37, 37 and 37% identical with that of human endothelial, rat macrophage, guinea-pig liver, human and rat keratinocyte transglutaminases, and the human blood-coagulation factor XIIIa subunit, respectively. The cDNA clone was hybridized to a single mRNA species of 3.9 kb in the liver, lung, spleen and heart but not hybridized to RNA from the brain. Northern-blot analysis of mRNA from retinoid-treated cultured vascular endothelial cells revealed that retinoids were able to induce a large increase in the transglutaminase mRNA levels.

引用

页码：15 / 21

页数：7

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