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RecA finds homologous DNA by reduced dimensionality search

Wiktor, Jakub (author)
Uppsala universitet,Molekylär systembiologi,Science for Life Laboratory, SciLifeLab
Gynnå, Arvid H., 1988- (author)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Molekylär systembiologi
Leroy, Prune (author)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Molekylär systembiologi
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Larsson, Jimmy, 1977- (author)
Uppsala universitet,Molekylär systembiologi,Science for Life Laboratory, SciLifeLab
Coceano, Giovanna (author)
KTH,Biofysik,Science for Life Laboratory, SciLifeLab,Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden
Testa, Ilaria (author)
KTH,Biofysik,Science for Life Laboratory, SciLifeLab,Department of Applied Physics, Science for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden
Elf, Johan (author)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Molekylär systembiologi
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 (creator_code:org_t)
2021-09-01
2021
English.
In: Nature. - : Springer Nature. - 0028-0836 .- 1476-4687. ; 597:7876, s. 426-429
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Homologous recombination is essential for the accurate repair of double-stranded DNA breaks (DSBs)1. Initially, the RecBCD complex2 resects the ends of the DSB into 3′ single-stranded DNA on which a RecA filament assembles3. Next, the filament locates the homologous repair template on the sister chromosome4. Here we directly visualize the repair of DSBs in single cells, using high-throughput microfluidics and fluorescence microscopy. We find that, in Escherichia coli, repair of DSBs between segregated sister loci is completed in 15 ± 5 min (mean ± s.d.) with minimal fitness loss. We further show that the search takes less than 9 ± 3 min (mean ± s.d) and is mediated by a thin, highly dynamic RecA filament that stretches throughout the cell. We propose that the architecture of the RecA filament effectively reduces search dimensionality. This model predicts a search time that is consistent with our measurement and is corroborated by the observation that the search time does not depend on the length of the cell or the amount of DNA. Given the abundance of RecA homologues5, we believe this model to be widely conserved across living organisms. 

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)

Keyword

cell
DNA
fluorescence
homology
microscopy
article
controlled study
double strand break repair
Escherichia coli
female
fluorescence microscopy
microfluidics
nonhuman
biological model
double stranded DNA break
enzymology
genetics
metabolism
recombination repair
sequence homology
time factor
bacterial DNA
RecA protein
single stranded DNA
DNA Breaks
Double-Stranded
DNA
Bacterial
DNA
Single-Stranded
Models
Biological
Rec A Recombinases
Recombinational DNA Repair
Sequence Homology
Nucleic Acid
Time Factors

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ref (subject category)
art (subject category)

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