scholarly journals FtsK functions in the processing of a Holliday junction intermediate during bacterial chromosome segregation

2000 ◽  
Vol 14 (23) ◽  
pp. 2976-2988 ◽  
Author(s):  
F.-X. Barre
2002 ◽  
Vol 56 (1) ◽  
pp. 567-597 ◽  
Author(s):  
Geoffrey C. Draper ◽  
James W. Gober

Cell ◽  
1997 ◽  
Vol 88 (5) ◽  
pp. 577-579 ◽  
Author(s):  
Robert T. Wheeler ◽  
Lucy Shapiro

2010 ◽  
Vol 29 (18) ◽  
pp. 3068-3081 ◽  
Author(s):  
Whitman B Schofield ◽  
Hoong Chuin Lim ◽  
Christine Jacobs-Wagner

Open Biology ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 200097 ◽  
Author(s):  
Adam S. B. Jalal ◽  
Tung B. K. Le

Proper chromosome segregation during cell division is essential in all domains of life. In the majority of bacterial species, faithful chromosome segregation is mediated by the tripartite ParABS system, consisting of an ATPase protein ParA, a CTPase and DNA-binding protein ParB, and a centromere-like parS site. The parS site is most often located near the origin of replication and is segregated first after chromosome replication. ParB nucleates on parS before binding to adjacent non-specific DNA to form a multimeric nucleoprotein complex. ParA interacts with ParB to drive the higher-order ParB–DNA complex, and hence the replicating chromosomes, to each daughter cell. Here, we review the various models for the formation of the ParABS complex and describe its role in segregating the origin-proximal region of the chromosome. Additionally, we discuss outstanding questions and challenges in understanding bacterial chromosome segregation.


2006 ◽  
Vol 20 (23) ◽  
pp. 3269-3282 ◽  
Author(s):  
M. A. Fogel ◽  
M. K. Waldor

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