Pericentrosomal Localization of the TIG3 Tumor Suppressor Requires an N-Terminal Hydrophilic Region Motif

被引:7
作者
Scharadin, Tiffany M. [1 ]
Adhikary, Gautam [1 ]
Shaw, Kristin [1 ]
Grun, Dan J. B. [1 ]
Xu, Wen [1 ]
Eckert, Richard L. [1 ,2 ,3 ]
机构
[1] Univ Maryland, Sch Med, Dept Biochem & Mol Biol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Dermatol, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Obstet & Gynecol & Reprod Sci, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
DOWN-REGULATION; BIOLOGICAL-ACTIVITY; I TRANSGLUTAMINASE; CANCER CELLS; GENE; RIG1; EXPRESSION; H-REV107; CLONING; DOMAIN;
D O I
10.1038/jid.2013.533
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Tazarotene-induced gene 3 (TIG3) is a tumor suppressor protein that has a key role in controlling cell proliferation. TIG3 is observed at reduced levels in epidermal squamous cell carcinoma, and the restoration of expression in skin cancer cells reduces cell survival. TIG3 suppresses cell survival through mechanisms that involve localization at the plasma membrane and at the centrosonne. TIG3 interacts at the plasma membrane to activate enzymes involved in keratinocyte terminal differentiation, and at the centrosome to inhibit daughter centrosome separation during mitosis leading to cessation of cell proliferation and induction of apoptosis. An important goal is identifying the motifs required for TIG3 localization at these intracellular sites as a method to understand the function of TIG3 at each location. TIG3 encodes an N-terminal hydrophilic region (amino acids 1-135) and a C-terminal membrane-anchoring domain (amino acids 135-164). We show that the C-terminal hydrophobic domain targets intact TIG3 to the plasma membrane, but when isolated as an independent element localizes at the mitochondria. We further demonstrate that a segment of the N-terminal hydrophilic region targets the centrosome. These studies provide important insights regarding the mechanisms that guide subcellular localization of this keratinocyte survival regulator.
引用
收藏
页码:1220 / 1229
页数:10
相关论文
共 31 条
[1]   Molecular cloning and biological activity of a novel Ha-ras suppressor gene predominantly expressed in skeletal muscle, heart, brain, and bone marrow by differential display using clonal mouse EC cells, ATDC5 [J].
Akiyama, H ;
Hiraki, Y ;
Noda, M ;
Shigeno, C ;
Ito, H ;
Nakamura, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32192-32197
[2]   Evolutionary history, structural features and biochemical diversity of the NlpC/P60 superfamily of enzymes [J].
Anantharaman, V ;
Aravind, L .
GENOME BIOLOGY, 2003, 4 (02)
[3]  
Deucher A, 2000, INT J ONCOL, V17, P1195
[4]   Identification and characterization of a retinoid-induced class II tumor suppressor growth regulatory gene [J].
DiSepio, D ;
Ghosn, C ;
Eckert, RL ;
Deucher, A ;
Robinson, N ;
Duvic, M ;
Chandraratna, RAS ;
Nagpal, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14811-14815
[5]   Chromosome segregation and aneuploidy series: Centrosome control of the cell [J].
Doxsey, S ;
Zimmerman, W ;
Mikule, K .
TRENDS IN CELL BIOLOGY, 2005, 15 (06) :303-311
[6]   Tazarotene-induced gene 3 is suppressed in basal cell carcinomas and reversed in vivo by tazarotene application [J].
Duvic, M ;
Ni, X ;
Talpur, R ;
Herne, K ;
Schulz, C ;
Sui, D ;
Ward, S ;
Joseph, A ;
Hazarika, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :902-909
[7]  
Duvic M, 2000, CLIN CANCER RES, V6, P3249
[8]  
Duvic M, 1997, J AM ACAD DERMATOL, V37, pS18
[9]   TIG3: a regulator of type I transglutaminase activity in epidermis [J].
Eckert, Richard L. ;
Sturniolo, Michael T. ;
Jans, Ralph ;
Kraft, Catherine A. ;
Jiang, Haibing ;
Rorke, Ellen A. .
AMINO ACIDS, 2009, 36 (04) :739-746
[10]  
HAJNAL A, 1994, ONCOGENE, V9, P479