Cell cycle arrest in era GTPase mutants:: a potential growth rate-regulated checkpoint in Escherichia coli

被引:113
作者
Britton, RA
Powell, BS
Dasgupta, S
Sun, Q
Margolin, W
Lupski, JR
Court, DL [1 ]
机构
[1] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Lab Gene Regulat & Chromosome Biol, Frederick, MD 21702 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Cell & Mol Biol Program, Houston, TX 77030 USA
[4] Univ Texas, Sch Med, Dept Microbiol & Mol Genet, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
关键词
D O I
10.1046/j.1365-2958.1998.00719.x
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
Era is a low-molecular-weight GTPase essential for Escherichia coli viability. The gene encoding Era is found in the me operon, and the synthesis of both RNase ill and Era increases with growth rate. Mutants that are partially defective in Era GTPase activity or that are reduced in the synthesis of wild-type Era become arrested in the cell cycle at the predivisional two-cell stage. The partially defective Era GTPase mutation (era1) suppresses several temperature-sensitive lethal alleles that affect chromosome replication and chromosome partitioning but not cell division. Our results suggest that Era plays an important role in cell cycle progression at a specific point in the cycle, after chromosome partitioning but before cytokinesis. Possible functions for Era in cell cycle progression and the initiation of cell division are discussed.
引用
收藏
页码:739 / 750
页数:12
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