A role for topoisomerase III in Escherichia coli chromosome segregation
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作者:
Perez-Cheeks, Brenda A.
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Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Perez-Cheeks, Brenda A.
[1
]
Lee, Chong
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Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Lee, Chong
[1
]
Hayama, Ryo
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Weill Cornell Grad Sch Med Sci, Physiol Biophys & Syst Biol Grad Program, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Hayama, Ryo
[2
]
Marians, Kenneth J.
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Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Marians, Kenneth J.
[1
]
机构:
[1] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
[2] Weill Cornell Grad Sch Med Sci, Physiol Biophys & Syst Biol Grad Program, New York, NY 10065 USA
The cellular function of Escherichia coli topoisomerase III remains elusive. We show that rescue of temperature-sensitive mutants in parE and parC (encoding the subunits of the chromosomal decatenase topoisomerase IV) at restrictive temperatures by high-copy suppressors is strictly dependent on topB (encoding topoisomerase III). Double mutants of parE Delta topB and parC Delta topB were barely viable, grew slowly, and were defective in chromosome segregation at permissive temperatures. The topB mutant phenotype did not result from accumulation of toxic recombination intermediates, because it was not relieved by mutations in either recQ or recA. In addition, in an otherwise wild-type genetic background, Delta topB cells treated with the type II topoisomerase inhibitor novobiocin displayed aberrant chromosome segregation. This novobiocin sensitivity was attributable to an increased demand for topoisomerase IV and is unlikely to define a new role for topoisomerase III; therefore, these results suggest that topoisomerase III participates in orderly and efficient chromosome segregation in E. coli.
机构:
Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Perez-Cheeks, Brenda A.
Lee, Chong
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h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Lee, Chong
Hayama, Ryo
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h-index: 0
机构:
Weill Cornell Grad Sch Med Sci, Physiol Biophys & Syst Biol Grad Program, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
Hayama, Ryo
Marians, Kenneth J.
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机构:
Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
机构:
Cornell Univ, Weill Grad Sch, Program Mol Biol, New York, NY 10065 USACornell Univ, Weill Grad Sch, Program Mol Biol, New York, NY 10065 USA
Madabhushi, Ram
Marians, Kenneth J.
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机构:
Cornell Univ, Weill Grad Sch, Program Mol Biol, New York, NY 10065 USA
Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USACornell Univ, Weill Grad Sch, Program Mol Biol, New York, NY 10065 USA
机构:
NCI, ABL Basic Res Program, Frederick Canc Res & Dev Ctr, Ft Detrick, MD 21702 USANCI, ABL Basic Res Program, Frederick Canc Res & Dev Ctr, Ft Detrick, MD 21702 USA
Sawitzke, JA
Austin, S
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机构:
NCI, ABL Basic Res Program, Frederick Canc Res & Dev Ctr, Ft Detrick, MD 21702 USANCI, ABL Basic Res Program, Frederick Canc Res & Dev Ctr, Ft Detrick, MD 21702 USA