Evidence map›Paper›PMID 25165823›Full record

ArticlePLoS genetics2014

Multiple regulation of Rad51-mediated homologous recombination by fission yeast Fbh1.

Yasuhiro Tsutsui, Yumiko Kurokawa, Kentaro Ito, Md Shahjahan P Siddique, Yumiko Kawano, Fumiaki Yamao, Hiroshi Iwasaki

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 42 citations in OpenAlex.

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  11. SCFNature communications · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Yasuhiro TsutsuiDepartment of Biological Sciences, School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Yumiko KurokawaEducation Academy of Computational Life Science, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Kentaro ItoDepartment of Biological Sciences, School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Md Shahjahan P SiddiqueDepartment of Biological Sciences, School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Yumiko KawanoDepartment of Biological Sciences, School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Fumiaki YamaoInternational Institute for Advanced Studies, Kizugawa, Kyoto, Japan.
Hiroshi IwasakiDepartment of Biological Sciences, School and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Meguro-ku, Tokyo, Japan.
Tokyo Institute of Technology · JPInternational Institute for Advanced Studies · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fbh1, an F-box helicase related to bacterial UvrD, has been proposed to modulate homologous recombination in fission yeast. We provide several lines of evidence for such modulation. Fbh1, but not the related helicases Srs2 and Rqh1, suppressed the formation of crossover recombinants from single HO-induced DNA double-strand breaks. Purified Fbh1 in complex with Skp1 (Fbh1-Skp1 complex) inhibited Rad51-driven DNA strand exchange by disrupting Rad51 nucleoprotein filaments in an ATP-dependent manner; this disruption was alleviated by the Swi5-Sfr1 complex, an auxiliary activator of Rad51. In addition, the reconstituted SCFFbh1 complex, composed of purified Fbh1-Skp1 and Pcu1-Rbx1, displayed ubiquitin-ligase E3 activity toward Rad51. Furthermore, Fbh1 reduced the protein level of Rad51 in stationary phase in an F-box-dependent, but not in a helicase domain-independent manner. These results suggest that Fbh1 negatively regulates Rad51-mediated homologous recombination via its two putative, unrelated activities, namely DNA unwinding/translocation and ubiquitin ligation. In addition to its anti-recombinase activity, we tentatively suggest that Fbh1 might also have a pro-recombination role in vivo, because the Fbh1-Skp1 complex stimulated Rad51-mediated strand exchange in vitro after strand exchange had been initiated.

Indexed as

CytoskeletonDNA Breaks, Double-StrandedDNA HelicasesHomologous RecombinationMutationNucleoproteinsRad51 RecombinaseSchizosaccharomycesSchizosaccharomyces pombe ProteinsSKP Cullin F-Box Protein LigasesUbiquitin-Protein LigasesDNA HelicasesFbh1 protein, S pombeNucleoproteinsRad51 RecombinaseRHP51 protein, S pombeSchizosaccharomyces pombe ProteinsSKP1 protein, S pombeSKP Cullin F-Box Protein LigasesUbiquitin-Protein Ligases

Identifiers

PMID25165823
PMCPMC4148199
OpenAlexW1989344535

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.