A Bacterial Chromosome Structuring Protein Binds Overtwisted DNA to Stimulate Type II Topoisomerases and Enable DNA Replication
Author(s) -
Monica S. Guo,
Diane L. Haakonsen,
Wenjie Zeng,
Maria A. Schumacher,
Michael T. Laub
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.08.029
Subject(s) - dna supercoil , dna gyrase , topoisomerase , biology , caulobacter crescentus , dna replication , circular bacterial chromosome , dna , prokaryotic dna replication , eukaryotic dna replication , dna clamp , dna polymerase , topoisomerase iv , replisome , origin of replication , control of chromosome duplication , dna polymerase ii , microbiology and biotechnology , genetics , rna , gene , escherichia coli , cell cycle , reverse transcriptase
When DNA is unwound during replication, it becomes overtwisted and forms positive supercoils in front of the translocating DNA polymerase. Unless removed or dissipated, this superhelical tension can impede replication elongation. Topoisomerases, including gyrase and topoisomerase IV in bacteria, are required to relax positive supercoils ahead of DNA polymerase but may not be sufficient for replication. Here, we find that GapR, a chromosome structuring protein in Caulobacter crescentus, is required to complete DNA replication. GapR associates in vivo with positively supercoiled chromosomal DNA, and our biochemical and structural studies demonstrate that GapR forms a dimer-of-dimers that fully encircles overtwisted DNA. Further, we show that GapR stimulates gyrase and topo IV to relax positive supercoils, thereby enabling DNA replication. Analogous chromosome structuring proteins that locate to the overtwisted DNA in front of replication forks may be present in other organisms, similarly helping to recruit and stimulate topoisomerases during DNA replication.
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