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
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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
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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
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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
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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:
Univ Washington, Dept Phys, Seattle, WA 98195 USA
Univ Washington, Dept Bioengn, Seattle, WA 98195 USAUniv Washington, Dept Phys, Seattle, WA 98195 USA
Kuwada, Nathan J.
Cheveralls, Keith C.
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Univ Calif Berkeley, Biophys Grad Grp, Berkeley, CA 94720 USAUniv Washington, Dept Phys, Seattle, WA 98195 USA
Cheveralls, Keith C.
Traxler, Beth
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Univ Washington, Dept Microbiol, Seattle, WA 98195 USAUniv Washington, Dept Phys, Seattle, WA 98195 USA
Traxler, Beth
Wiggins, Paul A.
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Univ Washington, Dept Phys, Seattle, WA 98195 USA
Univ Washington, Dept Bioengn, Seattle, WA 98195 USAUniv Washington, Dept Phys, Seattle, WA 98195 USA