4.8 Article

A biomechanical mechanism for initiating DNA packaging

期刊

NUCLEIC ACIDS RESEARCH
卷 42, 期 19, 页码 11921-11927

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gku896

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资金

  1. Natural Sciences and Engineering Research Council of Canada [RGPIN 418251-13]
  2. Canada Foundation for Innovation [PN 30735]
  3. Canadian Institutes for Health Research [MOP-86683, MSH-87729]

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The bacterial chromosome is under varying levels of mechanical stress due to a high degree of crowding and dynamic protein-DNA interactions experienced within the nucleoid. DNA tension is difficult to measure in cells and its functional significance remains unclear although in vitro experiments have implicated a range of biomechanical phenomena. Using single-molecule tools, we have uncovered a novel protein-DNA interaction that responds to fluctuations in mechanical tension by condensing DNA. We combined tethered particle motion (TPM) and optical tweezers experiments to probe the effects of tension on DNA in the presence of the Hha/H-NS complex. The nucleoid structuring protein H-NS is a key regulator of DNA condensation and gene expression in enterobacteria and its activity in vivo is affected by the accessory factor Hha. We find that tension, induced by optical tweezers, causes the rapid compaction of DNA in the presence of the Hha/H-NS complex, but not in the presence of H-NS alone. Our results imply that H-NS requires Hha to condense bacterial DNA and that this condensation could be triggered by the level of mechanical tension experienced along different regions of the chromosome.

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