Inhibition of protein synthesis by the T cell receptor-inducible human TDAG51 gene product

被引:32
作者
Hinz, T
Flindt, S
Marx, A
Janssen, O
Kabelitz, D
机构
[1] Paul Ehrlich Inst, Dept Immunol, D-63225 Langen, Germany
[2] Univ Kiel, Inst Immunol, D-24105 Kiel, Germany
关键词
apoptosis; TDAG51; T-lymphocytes; translation;
D O I
10.1016/S0898-6568(01)00141-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The T cell death associated gene 51 (TDAG51) was shown to be required for T cell receptor (TCR)-dependent induction of Fas/Apol/ CD95 expression in a murine T cell hybridoma. Despite the absence of a nuclear localization sequence and a nucleic acid binding domain, it was suggested to be localized in the nucleus and to function as a transcription factor regulating Fas-expression. However, we demonstrate that the human (h)TDAG51 protein is localized in the cytoplasm and the nucleoli, suggesting a role in ribosome biogenesis and;or translation regulation. Indeed, it strongly inhibited translation of a luciferase mRNA in a reticulocyte translational extract. Furthermore, cotransfection of hTDAG51 and the luciferase gene into 293T cells resulted in a strong inhibition of luciferase mRNA translation. Our findings were further strengthened by isolating in a yeast two-hybrid screen three proteins which are involved in the regulation of translation. Pie speculate that hTDAG51 couples TCR signaling to inhibition of protein biosynthesis in activated T lymphocytes. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:345 / 352
页数:8
相关论文
共 32 条
[1]   Structure of cDNAs encoding human eukaryotic initiation factor 3 subunits - Possible roles in RNA binding and macromolecular assembly [J].
Asano, K ;
Vornlocher, HP ;
RichterCook, NJ ;
Merrick, WC ;
Hinnebusch, AG ;
Hershey, JWB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (43) :27042-27052
[2]   Correction of respiratory burst activity in X-linked chronic granulomatous cells to therapeutically relevant levels after gene transfer into bone marrow CD34+ cells [J].
Becker, S ;
Wasser, S ;
Hauses, M ;
Hossle, JP ;
Ott, MG ;
Dinauer, MC ;
Ganser, A ;
Hoelzer, D ;
Seger, R ;
Grez, M .
HUMAN GENE THERAPY, 1998, 9 (11) :1561-1570
[3]   Degradation of eukaryotic polypeptide chain initiation factor (eIF) 4G in response to induction of apoptosis in human lymphoma cell lines [J].
Clemens, MJ ;
Bushell, M ;
Morley, SJ .
ONCOGENE, 1998, 17 (22) :2921-2931
[4]   Interaction of polyadenylate-binding protein with the eIF4G homologue PAIP enhances translation [J].
Craig, AWB ;
Haghighat, A ;
Yu, ATK ;
Sonenberg, N .
NATURE, 1998, 392 (6675) :520-523
[5]   AUTOCRINE T-CELL SUICIDE MEDIATED BY APO-1/(FAS/CD95) [J].
DHEIN, J ;
WALCZAK, H ;
BAUMLER, C ;
DEBATIN, KM ;
KRAMMER, PH .
NATURE, 1995, 373 (6513) :438-441
[6]   A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1:: tissue-specific expression, chromosomal location, and parental imprinting [J].
Frank, D ;
Mendelsohn, CL ;
Ciccone, E ;
Svensson, K ;
Ohlsson, R ;
Tycko, B .
MAMMALIAN GENOME, 1999, 10 (12) :1150-1159
[8]   A proline- and glutamine-rich protein promotes apoptosis in neuronal cells [J].
Gomes, I ;
Xiong, W ;
Miki, T ;
Rosner, MR .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (02) :612-622
[9]   DISCOVERY OF THE NUCLEOLAR TARGETING SIGNAL [J].
HATANAKA, M .
BIOESSAYS, 1990, 12 (03) :143-148
[10]   A novel form of DAP5 protein accumulates in apoptotic cells as a result of caspase cleavage and internal ribosome entry site-mediated translation [J].
Henis-Korenblit, S ;
Strumpf, NL ;
Goldstaub, D ;
Kimchi, A .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (02) :496-506