Pairing of P1 plasmid partition sites by ParB

Molecular Microbiology

Volumn 42, Issue 5, 2001, Pages 1363-1370

  Edgar, Rotem ^a   Chattoraj, Dhruba K ^a   Yarmolinsky, Michael ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; PROTEIN PARB; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL CHROMOSOME; CHROMOSOME PAIRING; DNA FLANKING REGION; IN VIVO STUDY; MITOSIS; MOLECULE; NONHUMAN; PLASMID; PRIORITY JOURNAL; SISTER CHROMATID;

BACTERIAL PROTEINS; BASE PAIRING; DNA, BACTERIAL; DNA, SUPERHELICAL; ESCHERICHIA COLI; PLASMIDS;

BACTERIA (MICROORGANISMS); PROKARYOTA;

EID: 0035724353     PISSN: 0950382X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2958.2001.02717.x     Document Type: Article

References (40)

1. Control of P1 plasmid replication by iterons
2. Partition of unit-copy miniplasmids to daughter cells. I. P1 and F miniplasmids contain discrete, interchangeable sequences sufficient to promote equipartition
3. A single 43-bp sopC repeat of plasmid mini-F is sufficient to allow assembly of a functional nucleoprotein partition complex
4. Partition functions of mini-F affect plasmid DNA topology in Escherichia coli
5. P1 ParA interacts with the P1 partition complex at parS and an ATP-ADP switch controls ParA activities
6. Stoichiometry of P1 plasmid partition complexes
7. Intracellular localization of P1 ParB protein depends on ParA and parS
8. Participation of Escherichia coli integration host factor in the P1 plasmid partition system
9. Mini-P1 plasmid partitioning: Excess ParB protein destabilizes plasmids containing the centromere parS
10. The P1 plasmid partition complex at parS. The influence of Escherichia coli integration host factor and of substrate topology
11. The P1 plasmid partition complex at parS. II. Analysis of ParB protein binding activity and specificity
12. Plasmid and chromosome partitioning: Surprises from phylogeny
13. Topological scanning of the P1 plasmid partition site
14. spo0J is required for normal chromosome segregation as well as the initiation of sporulation in Bacillus subtilis
15. Mechanism of DNA segregation in prokaryotes: Replicon pairing by parC of plasmid R1
16. Localization of F plasmid SopB protein to positions near the poles of Escherichia coli cells
17. Gene silencing via protein-mediated subcellular localization of DNA
18. P1 plasmid partition: A mutational analysis of ParB
19. Hybridization of DNA in dried gels provides increased sensitivity compared with hybridization to blots
20. Use of an inducible site-specific recombinase to probe the structure of protein-DNA complexes involved in F plasmid partition in Escherichia coli
21. SopB protein-mediated silencing of genes linked to the sopC locus of Escherichia coli F plasmid
22. Plasmid and chromosome segregation in prokaryotes
23. A series of wide-host-range low-copy-number vectors that allow direct screening for recombinants
24. Conformation of the origin of P1 plasmid replication. Initiator protein induced wrapping and intrinsic unstacking
25. Relaxation of replication control in chaperone-independent initiator mutants of plasmid P1
26. Mechanisms that contribute to the stable segregation of plasmids
27. Mini-F plasmid genes that couple host cell division to plasmid proliferation
28. On the mechanism of silencing in Escherichia coli
29. Silencing of genes flanking the P1 plasmid centromere
30. Mutants of Escherichia coli permeable to actinomycin
31. Heat shock proteins DnaJ, DnaK, and GrpE stimulate P1 plasmid replication by promoting initiator binding to the origin
32. Host/vector interactions which affect the viability of recombinant phage lambda clones
33. Active partitioning of bacterial plasmids
34. DNA looping alters local DNA conformation during transcription
35. Topological approaches to studies of protein-mediated looping of DNA in vivo
36. Transcription generates positively and negatively supercoiled domains in the template
37. Transcriptional silencing in bacteria
38. The F plasmid centromere, sopC, is required for full repression of the sopAB operon