New insights into the functions and localization of nuclear transglutaminase 2

被引:51
作者
Kuo, Ting-Fang [1 ,2 ]
Tatsukawa, Hideki [1 ]
Kojima, Soichi [1 ,2 ]
机构
[1] RIKEN Adv Sci Inst, Dept Biol Chem, Chem Genom Res Grp, Mol Ligand Biol Res Team, Wako, Saitama 3510198, Japan
[2] Tokyo Inst Technol, Dept Biol Sci, Grad Sch Biosci & Biotechnol, Tokyo, Japan
关键词
exportin; importin; nuclear localization; nuclear TG2; regulation of gene expression; TRANSCRIPTION FACTOR SP1; INITIATION-FACTOR; 5A; FACTOR-KAPPA-B; TISSUE-TYPE TRANSGLUTAMINASE; HUNTINGTONS-DISEASE; CROSS-LINKING; EXPORT SIGNALS; CELL-DEATH; INTRACELLULAR-LOCALIZATION; SUBCELLULAR-LOCALIZATION;
D O I
10.1111/j.1742-4658.2011.08409.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
Transglutaminase 2 (TG2; ) is the most abundantly expressed member of the transglutaminase family and exerts opposing effects on cell growth, differentiation and apoptosis via multiple activities, including transamidase, GTPase, cell adhesion, protein disulfide isomerase, kinase and scaffold activities. It is distributed in and around various parts of a cell, including the extracellular matrix, plasma membrane, cytosol, mitochondria and nucleus. Generally, nuclear TG2 represents only 57% of the total TG2 in a cell, and various stimuli will increase nuclear TG2 via cellular stress and/or an increased intracellular Ca2+ concentration. There is increasing evidence indicating the importance of nuclear TG2 in regulating gene expression via post-translational modification of (or interaction with) transcriptional factors and related proteins. These include E2F1, hypoxia inducible factor 1, Sp1 and histones. Through this mechanism, TG2 controls cell growth or survival, differentiation and apoptosis, and is involved in the pathogenesis and/or treatment of neurodegenerative diseases, liver diseases and cancers. The balance between import from the cytoplasm to the nucleus, and export from the nucleus to the cytoplasm, determines the level of TG2 in the nucleus. Selective regulation of the expression, activity or localization of nuclear TG2 will be important for basic research, as well as clinical applications, suggesting a new era for this long-studied enzyme.
引用
收藏
页码:4756 / 4767
页数:12
相关论文
共 93 条
[1]   Tissue transglutaminase-induced down-regulation of matrix metalloproteinase-9 [J].
Ahn, Jun-Seok ;
Kim, Min-kyung ;
Hahn, Jang-hee ;
Park, Jung-Hyeun ;
Park, Kyeong-Han ;
Cho, Byung-Ryul ;
Park, Seung-Bae ;
Kim, Dae-joong .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 376 (04) :743-747
[2]  
Akimov SS, 2001, J CELL SCI, V114, P2989
[3]   Tissue transglutaminase expression in HIV-Infected cells - An enzyme with an antiviral effect? [J].
Amendola, A ;
Rodolfo, C ;
Di Caro, A ;
Ciccosanti, F ;
Falasca, L ;
Piacentini, M .
HIV-ASSOCIATED CARDIOVASCULAR DISEASE: CLINICAL AND BIOLOGICAL INSIGHTS, 2001, 946 :108-120
[4]   Tissue transglutaminase contributes to disease progression in the R6/2 Huntington's disease mouse model via aggregate-independent mechanisms [J].
Bailey, CDC ;
Johnson, GVW .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (01) :83-92
[5]   Tissue-transglutaminase contributes to neutrophil granulocyte differentiation and functions [J].
Balajthy, Zoltan ;
Csomos, Krisztian ;
Vamosi, Gyrogy ;
Szanto, Attila ;
Lanotte, Michel ;
Fesus, Laszlo .
BLOOD, 2006, 108 (06) :2045-2054
[6]   Core histones are glutaminyl substrates for tissue transglutaminase [J].
Ballestar, E ;
Abad, C ;
Franco, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) :18817-18824
[7]   Extracellular TG2: emerging functions and regulation [J].
Belkin, Alexey M. .
FEBS JOURNAL, 2011, 278 (24) :4704-4716
[8]  
BIRCKBICHLER PJ, 1976, CANCER RES, V36, P2911
[9]   Tissue transglutaminase protects against apoptosis by modifying the tumor suppressor protein p110 Rb. [J].
Boehm, JE ;
Singh, U ;
Combs, C ;
Antonyak, MA ;
Cerione, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20127-20130
[10]   ADENOVIRUS-E1B 19-KDA AND BCL-2 PROTEINS INTERACT WITH A COMMON SET OF CELLULAR PROTEINS [J].
BOYD, JM ;
MALSTROM, S ;
SUBRAMANIAN, T ;
VENKATESH, LK ;
SCHAEPER, U ;
ELANGOVAN, B ;
DSAEIPPER, C ;
CHINNADURAI, G .
CELL, 1994, 79 (02) :341-351