Literature DB >> 22051117

New insights into the functions and localization of nuclear transglutaminase 2.

Ting-Fang Kuo1, Hideki Tatsukawa, Soichi Kojima.   

Abstract

Transglutaminase 2 (TG2; EC 2.3.2.13) 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 5-7% of the total TG2 in a cell, and various stimuli will increase nuclear TG2 via cellular stress and/or an increased intracellular Ca(2+) 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.
© 2011 The Authors Journal compilation © 2011 FEBS.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22051117     DOI: 10.1111/j.1742-4658.2011.08409.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  25 in total

Review 1.  Transglutaminase 2-mediated serotonylation in pulmonary hypertension.

Authors:  K C Penumatsa; B L Fanburg
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2013-12-27       Impact factor: 5.464

2.  Effect of Some Growth Factors on Tissue Transglutaminase Overexpression Induced by β-Amyloid in Olfactory Ensheathing Cells.

Authors:  Rosalia Pellitteri; Roberta Bonfanti; Michela Spatuzza; Maria Teresa Cambria; Mariacristina Ferrara; Giuseppina Raciti; Agata Campisi
Journal:  Mol Neurobiol       Date:  2016-10-18       Impact factor: 5.590

Review 3.  Anti-type 2 transglutaminase antibodies as modulators of type 2 transglutaminase functions: a possible pathological role in celiac disease.

Authors:  Stefania Martucciello; Gaetana Paolella; Carla Esposito; Marilena Lepretti; Ivana Caputo
Journal:  Cell Mol Life Sci       Date:  2018-08-22       Impact factor: 9.261

Review 4.  Transglutaminase is a therapeutic target for oxidative stress, excitotoxicity and stroke: a new epigenetic kid on the CNS block.

Authors:  Manuela Basso; Rajiv R Ratan
Journal:  J Cereb Blood Flow Metab       Date:  2013-04-10       Impact factor: 6.200

Review 5.  Transglutaminase regulation of cell function.

Authors:  Richard L Eckert; Mari T Kaartinen; Maria Nurminskaya; Alexey M Belkin; Gozde Colak; Gail V W Johnson; Kapil Mehta
Journal:  Physiol Rev       Date:  2014-04       Impact factor: 37.312

Review 6.  Physiological, pathological, and structural implications of non-enzymatic protein-protein interactions of the multifunctional human transglutaminase 2.

Authors:  Kajal Kanchan; Mónika Fuxreiter; László Fésüs
Journal:  Cell Mol Life Sci       Date:  2015-05-06       Impact factor: 9.261

Review 7.  Extracellular TG2: emerging functions and regulation.

Authors:  Alexey M Belkin
Journal:  FEBS J       Date:  2011-11-21       Impact factor: 5.542

8.  The proinflammatory protein HMGB1 is a substrate of transglutaminase-2 and forms high-molecular weight complexes with autoantigens.

Authors:  William L Willis; Linan Wang; Takuma Tsuzuki Wada; Mark Gardner; Omar Abdouni; Jeffrey Hampton; Giancarlo Valiente; Nicholas Young; Stacy Ardoin; Sudha Agarwal; Michael A Freitas; Lai-Chu Wu; Wael N Jarjour
Journal:  J Biol Chem       Date:  2018-04-04       Impact factor: 5.157

9.  Lamin aggregation is an early sensor of porphyria-induced liver injury.

Authors:  Amika Singla; Nicholas W Griggs; Raymond Kwan; Natasha T Snider; Dhiman Maitra; Stephen A Ernst; Harald Herrmann; M Bishr Omary
Journal:  J Cell Sci       Date:  2013-05-02       Impact factor: 5.285

10.  Nuclear Transglutaminase 2 interacts with topoisomerase II⍺ to promote DNA damage repair in lung cancer cells.

Authors:  Xiao Lei; Kun Cao; Yuanyuan Chen; Hui Shen; Zhe Liu; Hongran Qin; Jianming Cai; Fu Gao; Yanyong Yang
Journal:  J Exp Clin Cancer Res       Date:  2021-07-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.