A role for the common GTP-binding protein in coupling of chromosome replication to cell growth and cell division

被引:21
作者
Sikora-Borgula, A
Slominska, M
Trzonkowski, P
Zielke, R
Mysliwski, A
Wegrzyn, G
Czyz, A
机构
[1] Univ Gdansk, Mol Biol Lab, Dept Mol Biol, PL-80822 Gdansk, Poland
[2] Med Univ Gdansk, Dept Histol & Immunol, PL-80210 Gdansk, Poland
[3] Polish Acad Sci, Inst Oceanol, PL-81347 Gdynia, Poland
[4] Univ Gdansk, Polish Acad Sci, Inst Biochem & Biophys, Mol Biol Lab, PL-80822 Gdansk, Poland
关键词
GTP-binding proteins; CgtA protein; Obg/Gtp1 subfamily of proteins; DNA replication; cell growth; cell division; flow cytometry;
D O I
10.1006/bbrc.2002.6671
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Homologues of CgtA, the common GTP-binding protein of Vibrio harveyi, are present in diverse organisms ranging from bacteria to humans. In bacteria, proteins homologous to CgtA form a subfamily of small GTP-binding proteins, called Obg/Gtp1. Similarity between bacterial members of this subfamily and their eukaryotic homologues is as high as about 50%. Nevertheless, specific functions of these proteins remain largely unknown. Genes coding for CgtA-like proteins are essential in almost all species of bacteria. The only known exception is V. harveyi, whose cells survive disruption of the cgtA gene. Therefore, the V. harveyi cgtA insertional mutant is a very useful tool for studies on functions of CgtA. Here we demonstrate that under normal growth conditions, cells of the cgtA mutant are slightly larger than wild-type cells, whereas indirect inhibition of DNA replication initiation by addition of rifampicin results in significantly higher differences in average cell size between these two strains as measured by flow cytometry. These differences decreased when cell division was inhibited by cephalexin. DNA synthesis per cell mass was found to be increased in the cgtA mutant relative to wild-type V. harveyi strain, whereas the mutant cells grew slower than bacteria with functional cgtA gene. Kinetics of DNA replication after inhibition of cell division was also considerably different in wild-type and cgtA mutant strains. These results suggest that the cgtA gene product plays a role in coupling of DNA replication to cell growth and cell division. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:333 / 338
页数:6
相关论文
共 24 条
[1]   A genome-based approach for the identification of essential bacterial genes [J].
Arigoni, F ;
Talabot, F ;
Peitsch, M ;
Edgerton, MD ;
Meldrum, E ;
Allet, E ;
Fish, R ;
Jamotte, T ;
Curchod, ML ;
Loferer, H .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :851-856
[2]   BACTERIAL BIOLUMINESCENCE - ISOLATION AND EXPRESSION OF THE LUCIFERASE GENES FROM VIBRIO-HARVEYI [J].
BELAS, R ;
MILEHAM, A ;
COHN, D ;
HILMEN, M ;
SIMON, M ;
SILVERMAN, M .
SCIENCE, 1982, 218 (4574) :791-793
[3]  
Brocchieri L, 2000, PROTEIN SCI, V9, P476
[4]   Vibrio harveyi bioluminescence plays a role in stimulation of DNA repair [J].
Czyz, A ;
Wróbel, B ;
Wegrzyn, G .
MICROBIOLOGY-SGM, 2000, 146 :283-288
[5]  
Czyz A, 2001, MICROBIOL-UK, V147, P183
[6]   Genetically modified Vibrio harveyi strains as potential bioindicators of mutagenic pollution of marine environments [J].
Czyz, A ;
Jasiecki, J ;
Bogdan, A ;
Szpilewska, H ;
Wegrzyn, G .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (02) :599-605
[7]   Heat-shock proteins, molecular chaperones, and the stress response: Evolutionary and ecological physiology [J].
Feder, ME ;
Hofmann, GE .
ANNUAL REVIEW OF PHYSIOLOGY, 1999, 61 :243-282
[8]  
Helmstetter C., 1996, Escherichia coli and Salmonella, P1627
[9]   Heat shock protein 70 family: Multiple sequence comparisons, function, and evolution [J].
Karlin, S ;
Brocchieri, L .
JOURNAL OF MOLECULAR EVOLUTION, 1998, 47 (05) :565-577
[10]   CHARACTERIZATION OF HEAT-SHOCK RESPONSE OF THE MARINE BACTERIUM VIBRIO-HARVEYI [J].
KLEIN, G ;
WALCZAK, R ;
KRASNOWSKA, E ;
BLASZCZAK, A ;
LIPINSKA, B .
MOLECULAR MICROBIOLOGY, 1995, 16 (04) :801-811