Transfection-mediated cell-cycle signaling: Considerations for transient transfection-based cell-cycle studies

被引:29
作者
Rodriguez, A
Flemington, EK
机构
[1] Harvard Univ, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
apoptosis; transfection; p53; cell cycle;
D O I
10.1006/abio.1999.4156
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transient transfection of recombinant genes into cells is a commonly used approach for analyzing cell-cycle- and/or apoptotic-related activities of cell-cycle control proteins. In this approach, information regarding the functional consequence of expressing a recombinant protein transiently is garnered by comparing against results obtained from cells which are transfected with either a control expression plasmid and/or with mutant expression plasmids. In general however, little attention is paid to whether the transfection procedure itself influences these experiments. Using the calcium phosphate transfection method, we show that the introduction of DNA into cells induces signaling of the cell-cycle control machinery. In Hela cells, a transient increase in G0/G1 cells is observed 8 h after transfection. Furthermore, the introduction of DNA into several cell lines induces apoptosis. Transfection-mediated apoptosis can be elicited through a p53-independent mechanism, suggesting the possible extrapolation to many tumor cell lines. Last, we show that due to a likely cell-cycle-specific entry of marker genes into the nucleus, a highly biased cell-cycle distribution is observed in successfully transfected cells at early times following transfection. The importance of these issues in the interpretation as well as the design of transient transfection-based cell-cycle experiments is discussed. (C) 1999 Academic Press.
引用
收藏
页码:171 / 181
页数:11
相关论文
共 16 条
[1]   The Epstein-Barr virus bZIP transcription factor Zta causes G(0)/G(1) cell cycle arrest through induction of cyclin-dependent kinase inhibitors [J].
Cayrol, C ;
Flemington, EK .
EMBO JOURNAL, 1996, 15 (11) :2748-2759
[2]   RANDOM SUBCLONING OF SONICATED DNA - APPLICATION TO SHOTGUN DNA-SEQUENCE ANALYSIS [J].
DEININGER, PL .
ANALYTICAL BIOCHEMISTRY, 1983, 129 (01) :216-223
[3]   Cell death and cancer: replacement of apoptotic genes and inactivation of death suppressor genes in therapy [J].
Favrot, M ;
Coll, JL ;
Louis, N ;
Negoescu, A .
GENE THERAPY, 1998, 5 (06) :728-739
[4]   MDM2 GENE AMPLIFICATION AND TRANSCRIPT LEVELS IN HUMAN SARCOMAS - RELATIONSHIP TO TP53 GENE STATUS [J].
FLORENES, VA ;
MAELANDSMO, GM ;
FORUS, A ;
ANDREASSEN, A ;
MYKLEBOST, O ;
FODSTAD, O .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (17) :1297-1302
[5]  
FRANGIONI JV, 1994, J CELL SCI, V107, P827
[6]   Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers [J].
Kaghad, M ;
Bonnet, H ;
Yang, A ;
Creancier, L ;
Biscan, JC ;
Valent, A ;
Minty, A ;
Chalon, P ;
Lelias, JM ;
Dumont, X ;
Ferrara, P ;
McKeon, F ;
Caput, D .
CELL, 1997, 90 (04) :809-819
[7]  
Kalejta RF, 1997, CYTOMETRY, V29, P286, DOI 10.1002/(SICI)1097-0320(19971201)29:4<286::AID-CYTO4>3.0.CO
[8]  
2-8
[9]   Viral oncoproteins discriminate between p53 and the p53 homolog p73 [J].
Marin, MC ;
Jost, CA ;
Irwin, MS ;
DeCaprio, JA ;
Caput, D ;
Kaelin, WG .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6316-6324
[10]  
Morgenstern J P, 1991, Methods Mol Biol, V7, P181, DOI 10.1385/0-89603-178-0:181