Evidence map›Paper›PMID 21030440›Full record

ArticleNucleic acids research2011

Meiotic recombination protein Rec12: functional conservation, crossover homeostasis and early crossover/non-crossover decision.

Fengling Kan, Mari K Davidson, Wayne P Wahls

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Intragenic meiotic recombination in Schizosaccharomyces pombe is sensitive to environmental temperature changes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2020
    Article
  7. DNA Helicase Mph1Developmental cell · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Mechanism and regulation of meiotic recombination initiation.Cold Spring Harbor perspectives in biology · 2014
    Review
  16. Article
  17. DNA repair pathways in trypanosomatids: from DNA repair to drug resistance.Microbiology and molecular biology reviews : MMBR · 2014
    Review
  18. Article
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Fengling KanDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, 4301 West Markham Street (slot 516), Little Rock, AR 72205-7199, USA.
Mari K Davidson
Wayne P Wahls
University of Arkansas for Medical Sciences · US

Funding

Biochemistry of recombination in meiosisR01GM081766 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI WAHLS, WAYNE P · 2007 to 2018
$2.5M
Molecular mechanisms of aneuploidyR01ES013787 · NIEHS · UNIV OF ARKANSAS FOR MED SCIS · PI DAVIDSON, MARI K · 2005 to 2007
$951k
NIEHS NIH HHS ES13787NIGMS NIH HHS GM81766NIGMS NIH HHS R01 GM081766
6 · The paper itself

Abstract

In fission yeast and other eukaryotes, Rec12 (Spo11) is thought to catalyze the formation of dsDNA breaks (DSBs) that initiate homologous recombination in meiosis. Rec12 is orthologous to the catalytic subunit of topoisomerase VI (Top6A). Guided by the crystal structure of Top6A, we engineered the rec12 locus to encode Rec12 proteins each with a single amino acid substitution in a conserved residue. Of 21 substitutions, 10 significantly reduced or abolished meiotic DSBs, gene conversion, crossover recombination and the faithful segregation of chromosomes. Critical residues map within the metal ion-binding pocket toprim (E179A, D229A, D231A), catalytic region 5Y-CAP (R94A, D95A, Y98F) and the DNA-binding interface (K201A, G202E, R209A, K242A). A subset of substitutions reduced DSBs but maintained crossovers, demonstrating crossover homeostasis. Furthermore, a strong separation of function mutation (R304A) suggests that the crossover/non-crossover decision is established early by a protein-protein interaction surface of Rec12. Fission yeast has multiple crossovers per bivalent, and chromosome segregation was robust above a threshold of about one crossover per bivalent, below which non-disjunction occurred. These results support structural and functional conservation among Rec12/Spo11/Top6A family members for the catalysis of DSBs, and they reveal how Rec12 regulates other features of meiotic chromosome dynamics.

Indexed as

Recombination, GeneticAmino Acid SequenceArchaeal ProteinsChromosome SegregationDNA Breaks, Double-StrandedDNA Topoisomerases, Type IIGene ConversionHomeostasisMeiosisMeiotic Recombination Protein SPO11Molecular Sequence DataMutagenesis, Site-DirectedSchizosaccharomyces pombe ProteinsArchaeal ProteinsDNA Topoisomerases, Type IIDNA topoisomerase VIMeiotic Recombination Protein SPO11rec12 protein, S pombeSchizosaccharomyces pombe Proteins

Identifiers

PMID21030440
PMCPMC3045620
OpenAlexW2013250916

What OpenQuestion holds

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LicenceCC BY-NC
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.