Coding sequence, exon-intron structure and chromosomal localization of murine TNF-stimulated gene 6 that is specifically expressed by expanding cumulus cell-oocyte complexes

被引:107
作者
Fülöp, C
Kamath, RV
Li, YF
Otto, JM
Salustri, A
Olsen, BR
Glant, TT
Hascall, VC
机构
[1] Cleveland Clin Fdn, Dept Biomed Engn, Cleveland, OH 44195 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[4] Univ Roma Tor Vergata, Dept Publ Hlth & Cell Biol, I-00173 Rome, Italy
[5] Rush Presbyterian St Lukes Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
关键词
gene structure; gene expression;
D O I
10.1016/S0378-1119(97)00459-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tumor necrosis factor stimulated gene-6 (TSG-6) has been previously shown to be induced in vitro in several cell types by proinflammatory cytokines, and in vivo in pathological conditions such as rheumatoid arthritis. In this study, we report the complete coding sequence for the mouse TSG-6 protein, and the exon-intron structure and the chromosomal localization of the gene. We have identified a 1605 nt cDNA. sequence from mouse cumulus cell-oocyte complexes (COCs) induced to expand in vivo. The sequence contains an open reading frame of 825 nt that codes for the 275 amino acid TSG-6 protein. The gene contains six exons separated by 1.1-5.8 kb introns and has been localized to the murine chromosome 2 by linkage analysis. Comparative reverse transcription-polymerase chain reaction studies have revealed that TSG-6 mRNA is specifically expressed after COC expansion induced in vivo, identifying the first non-pathological process in which TSG-6 may play an important role. Since TSG-6 binds to hyaluronan and interacts with inter-alpha-trypsin inhibitor (I alpha I), molecules that are essential for matrix formation by COCs, this protein may have a structural role in the matrix or may enhance the antiproteolytic effect of I alpha I to protect the matrix from degradation. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:95 / 102
页数:8
相关论文
共 29 条
[1]   THE CUB DOMAIN - A WIDESPREAD MODULE IN DEVELOPMENTALLY-REGULATED PROTEINS [J].
BORK, P ;
BECKMANN, G .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 231 (02) :539-545
[2]  
CAMAIONI A, 1993, J BIOL CHEM, V268, P20473
[3]  
CHEN L, 1992, J BIOL CHEM, V267, P12380
[4]  
CHEN L, 1994, J BIOL CHEM, V269, P28282
[5]   GENE FOR A MAJOR CELL-SURFACE GLYCOPROTEIN OF MOUSE MACROPHAGES AND OTHER PHAGOCYTIC-CELLS IS ON CHROMOSOME-2 [J].
COLOMBATTI, A ;
HUGHES, EN ;
TAYLOR, BA ;
AUGUST, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :1926-1929
[6]   Human/mouse homology relationships [J].
DeBry, RW ;
Seldin, MF .
GENOMICS, 1996, 33 (03) :337-351
[7]  
FENG P, 1993, J BIOL CHEM, V268, P9387
[8]  
FENG P, 1993, J BIOL CHEM, V268, P21453
[9]  
FINELLI AL, 1994, DEVELOPMENT, V120, P861
[10]   Proteoglycans of the extracellular environment: Clues from the gene and protein side offer novel perspectives in molecular diversity and function [J].
Iozzo, RV ;
Murdoch, AD .
FASEB JOURNAL, 1996, 10 (05) :598-614