Evidence map›Paper›PMID 24062528›Full record

ArticleG3 (Bethesda, Md.)2013

A mutation in the FHA domain of Coprinus cinereus Nbs1 Leads to Spo11-independent meiotic recombination and chromosome segregation.

K Nicole Crown, Oleksandr P Savytskyy, Shehre-Banoo Malik, John Logsdon, R Scott Williams, John A Tainer, Miriam E Zolan

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. The meiotic checkpoint network: step-by-step through meiotic prophase.Cold Spring Harbor perspectives in biology · 2014
    Review
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 4 institutions in 1 country.

K Nicole CrownDepartment of Biology, Indiana University, Bloomington, Indiana 47405.
Oleksandr P Savytskyy
Shehre-Banoo Malik
John Logsdon
R Scott Williams
John A Tainer
Miriam E Zolan
Indiana University Bloomington · USUniversity of Iowa · USNational Institute of Environmental Health Sciences · USScripps Research Institute · US

Funding

Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI WALTER J. CHAZIN · 2001 to 2026
$89.6M
Structural Biology of Genome Maintenance and DNA repairZIAES102765 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WILLIAMS, ROBERT · 2010 to 2025
$35.2M
Mre11/Rad50 Structural Biology for DNA Damage ResponsesR01CA117638 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUSSELL, PAUL, TAINER, JOHN A. · 2005 to 2019
$5.6M
RADIATION REPAIR AND MEIOSIS IN COPRINUS CINEREUSR01GM043930 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI ZOLAN, MIRIAM E · 1995 to 2009
$2.7M
RADIATION REPAIR AND MEIOSIS IN COPRINUS CINEREUSR29GM043930 · NIGMS · INDIANA UNIVERSITY BLOOMINGTON · PI ZOLAN, MIRIAM E · 1990 to 1994
–
Intramural NIH HHS ZIA ES102765NCI NIH HHS CA117638NCI NIH HHS CA92584NCI NIH HHS P01 CA092584NCI NIH HHS R01 CA117638NIEHS NIH HHS 1Z01ES102765-01NIGMS NIH HHS GM43930NIGMS NIH HHS R01 GM043930
6 · The paper itself

Abstract

Nbs1, a core component of the Mre11-Rad50-Nbs1 complex, plays an essential role in the cellular response to DNA double-strand breaks (DSBs) and poorly understood roles in meiosis. We used the basidiomycete Coprinus cinereus to examine the meiotic roles of Nbs1. We identified the C. cinereus nbs1 gene and demonstrated that it corresponds to a complementation group previously known as rad3. One allele, nbs1-2, harbors a point mutation in the Nbs1 FHA domain and has a mild spore viability defect, increased frequency of meiosis I nondisjunction, and an altered crossover distribution. The nbs1-2 strain enters meiosis with increased levels of phosphorylated H2AX, which we hypothesize represent unrepaired DSBs formed during premeiotic replication. In nbs1-2, there is no apparent induction of Spo11-dependent DSBs during prophase. We propose that replication-dependent DSBs, resulting from defective replication fork protection and processing by the Mre11-Rad50-Nbs1 complex, are competent to form meiotic crossovers in C. cinereus, and that these crossovers lead to high levels of faithful chromosome segregation. In addition, although crossover distribution is altered in nbs1-2, the majority of crossovers were found in subtelomeric regions, as in wild-type. Therefore, the location of crossovers in C. cinereus is maintained when DSBs are induced via a Spo11-independent mechanism.

Indexed as

AllelesChromosomesChromosome SegregationCoprinusDNA Breaks, Double-StrandedDNA RepairEndodeoxyribonucleasesFungal ProteinsGenotypeHistonesMeiosisMeiotic Recombination Protein SPO11MutationNuclear ProteinsPhosphorylationPhylogenyEndodeoxyribonucleasesFungal ProteinsHistonesMeiotic Recombination Protein SPO11Nuclear ProteinsCoprinus cinereusDNA replicationmeiosisMRN complexrecombination

Identifiers

PMID24062528
PMCPMC3815056
OpenAlexW2116054829

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.