Chromosome 6 encoded RNaseT2 protein is a cell growth regulator

被引:12
作者
Liu, Jinglan [1 ]
Zhawar, Vikramjit K. [1 ]
Kaur, Gurpreet [1 ]
Kaur, G. Pal [1 ]
deRiel, Jon Kimball [1 ]
Kandpal, Raj P. [2 ]
Athwal, Raghbir S. [1 ]
机构
[1] Temple Univ, Fels Inst Canc Res & Mol Biol, Sch Med, Philadelphia, PA 19140 USA
[2] Western Univ Hlth Sci, Dept Basic Med Sci, Pomona, CA USA
关键词
RNaseT2; 6q27; cell senescence; cell growth regulation; cell immortalization; HUMAN MEMBER; SENESCENCE; TUMOR; GENE; CLONING; KINASE; FAMILY; REGION; AKT; IDENTIFICATION;
D O I
10.1111/j.1582-4934.2009.00749.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously shown by chromosome transfer technique that chromosome 6 alters the phenotype of a variety of tumour cells and SV40 immortalized cells. We present here the phenotypic effects of the ectopic expression of RNaseT2, a highly conserved ribonuclease encoded by chromosome 6q27, in SV40 immortalized cell lines. We contrast our findings with those reported for ovarian carcinoma cell lines and an SV40 immortalized cell line transfected with RNaseT2. Although RNaseT2 expression is elevated in normal diploid fibroblasts approaching senescence (passage 64), forced expression of the gene in immortalized cells does not cause them to senesce. A significant reduction was observed in colony forming efficiency, anchorage independence and growth rate of cells transfected with RNaseT2. The levels of transcripts involved in Akt signalling pathway, cell cycle control and pathways related to cell proliferation decreased 2-10-folds in SV40 immortalized cells in response to RNaseT2 expression. Interestingly, some immortalized cells expressed alternatively spliced transcript variants instead of the full-length RNaseT2 transcript. Our results are consistent with the conclusion that RNaseT2 is a cell growth regulator and it does not induce senescence in SV40 immortalized cell lines.
引用
收藏
页码:1146 / 1155
页数:10
相关论文
共 31 条
[1]  
Acquati F, 2005, INT J ONCOL, V26, P1159
[2]   Cloning and characterization of a senescence inducing and class II tumor suppressor gene in ovarian carcinoma at chromosome region 6q27 [J].
Acquati, F ;
Morelli, C ;
Cinquetti, R ;
Bianchi, MG ;
Porrini, D ;
Varesco, L ;
Gismondi, V ;
Rocchetti, R ;
Talevi, S ;
Possati, L ;
Magnanini, C ;
Tibiletti, MG ;
Bernasconi, B ;
Daidone, MG ;
Shridhar, V ;
Smith, DI ;
Negrini, M ;
Barbanti-Brodano, G ;
Taramelli, R .
ONCOGENE, 2001, 20 (08) :980-988
[3]   Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha [J].
Alessi, DR ;
James, SR ;
Downes, CP ;
Holmes, AB ;
Gaffney, PRJ ;
Reese, CB ;
Cohen, P .
CURRENT BIOLOGY, 1997, 7 (04) :261-269
[4]   Perturbations of the AKT signaling pathway in human cancer [J].
Altomare, DA ;
Testa, JR .
ONCOGENE, 2005, 24 (50) :7455-7464
[5]   CELL ENLARGEMENT - ONE POSSIBLE MECHANISM UNDERLYING CELLULAR SENESCENCE [J].
ANGELLO, JC ;
PENDERGRASS, WR ;
NORWOOD, TH ;
PROTHERO, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 140 (02) :288-294
[6]  
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[7]   Characterization of RNASET2, the first human member of the Rh/T2/S family of glycoproteins [J].
Campomenosi, P ;
Salis, S ;
Lindqvist, C ;
Mariani, D ;
Nordstrom, T ;
Acquati, F ;
Taramelli, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2006, 449 (1-2) :17-26
[8]   SEQUENCE VARIABILITY AND DEVELOPMENTAL EXPRESSION OF S-ALLELES IN SELF-INCOMPATIBLE AND PSEUDO-SELF-COMPATIBLE PETUNIA [J].
CLARK, KR ;
OKULEY, JJ ;
COLLINS, PD ;
SIMS, TL .
PLANT CELL, 1990, 2 (08) :815-826
[9]   A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[10]   Regulation of the Akt kinase by interacting proteins [J].
Du, KY ;
Tsichlis, PN .
ONCOGENE, 2005, 24 (50) :7401-7409