Transgelin: An actin-binding protein and tumour suppressor

被引:216
作者
Assinder, Stephen J. [1 ,2 ]
Stanton, Jo-Ann L. [3 ]
Prasad, Priya D. [3 ]
机构
[1] Univ Sydney, Discipline Physiol, Sch Med Sci, Sydney, NSW 2006, Australia
[2] Univ Sydney, Bosch Inst, Sydney, NSW 2006, Australia
[3] Univ Otago, Dept Anat & Struct Biol, Sch Med Sci, Dunedin, New Zealand
关键词
Transgelin; SM22; TGF-beta; MMP-9; Cancer; SMOOTH-MUSCLE-CELLS; TRANSCRIPTION FACTORS; HUMAN SM22; IN-VIVO; SM22-ALPHA; EXPRESSION; GENE; CALPONIN; GROWTH; MICE;
D O I
10.1016/j.biocel.2008.02.011
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
Transgelin is a shape change sensitive 22 kDa actin-binding protein of the calponin family. It contains a C-terminal calponin-like module (CLIK'-;) and an upstream positively charged amino acid region required for actin binding. Transgelin is ubiquitous to vascular and visceral smooth muscle and is an early marker of smooth muscle differentiation, where its expression is driven by CArG box. smooth muscle gene promoter. It is also present in fibroblasts, and some epithelium where expression is likely driven by TGF-beta 1. Transgelin null mice reveal that, whilst it is not required for smooth muscle development, transgelin may be involved in calcium-independent smooth muscle contraction. Recent evidence suggests that transgelin acts as a tumour suppressor. Its expression is lost in prostate, breast and colon cancers. This is consistent with suppression of the metallo matrix protease-9 (MMP-9) by transgelin, where MMP-9 is upregulated in these common cancers. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:482 / 486
页数:5
相关论文
共 27 条
[1]   Positive- and negative-acting Kruppel-like transcription factors bind a transforming growth factor β control element required for expression of the smooth muscle cell differentiation marker SM22α in vivo [J].
Adam, PJ ;
Regan, CP ;
Hautmann, MB ;
Owens, GK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37798-37806
[2]   CHARACTERIZATION OF THE GENE FOR MP20 - A DROSOPHILA MUSCLE PROTEIN THAT IS NOT FOUND IN ASYNCHRONOUS OSCILLATORY FLIGHT-MUSCLE [J].
AYMESOUTHGATE, A ;
LASKO, P ;
FRENCH, C ;
PARDUE, ML .
JOURNAL OF CELL BIOLOGY, 1989, 108 (02) :521-531
[3]   Expression and cytogenetic localization of the human SM22 gene (TAGLN) [J].
Camoretti-Mercado, B ;
Forsythe, SM ;
LeBeau, MM ;
Espinosa, R ;
Vieira, JE ;
Halayko, AJ ;
Willadsen, S ;
Kurtz, B ;
Ober, C ;
Evans, GA ;
Thweatt, R ;
Shapiro, S ;
Niu, Q ;
Qin, YM ;
Padrid, PA ;
Solway, J .
GENOMICS, 1998, 49 (03) :452-457
[4]   Smad proteins regulate transcriptional induction of the SM22α gene by TGF-β [J].
Chen, SY ;
Kulik, M ;
Lechleider, RJ .
NUCLEIC ACIDS RESEARCH, 2003, 31 (04) :1302-1310
[5]  
Danninger C, 2000, J CELL SCI, V113, P3725
[6]   Mutagenesis analysis of human SM22: characterization of actin binding [J].
Fu, YP ;
Liu, HW ;
Forsythe, SM ;
Kogut, P ;
McConville, JF ;
Halayko, AJ ;
Camoretti-Mercado, B ;
Solway, J .
JOURNAL OF APPLIED PHYSIOLOGY, 2000, 89 (05) :1985-1990
[7]   CALPONIN AND SM-22 ISOFORMS IN AVIAN AND MAMMALIAN SMOOTH-MUSCLE - ABSENCE OF PHOSPHORYLATION INVIVO [J].
GIMONA, M ;
SPARROW, MP ;
STRASSER, P ;
HERZOG, M ;
SMALL, JV .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (03) :1067-1075
[8]   Calponin repeats regulate actin filament stability and formation of podosomes in smooth muscle cells [J].
Gimona, M ;
Kaverina, I ;
Resch, GP ;
Vignal, E ;
Burgstaller, G .
MOLECULAR BIOLOGY OF THE CELL, 2003, 14 (06) :2482-2491
[9]   THE CAENORHABDITIS-ELEGANS MUSCLE-AFFECTING GENE UNC-87 ENCODES A NOVEL THIN FILAMENT-ASSOCIATED [J].
GOETINCK, S ;
WATERSTON, RH .
JOURNAL OF CELL BIOLOGY, 1994, 127 (01) :79-93
[10]  
Je HD, 2007, MOL CELLS, V23, P175