Evidence map›Paper›PMID 12437782›Full record

ArticleCell & chromosome2002

Distinct functions of S. pombe Rec12 (Spo11) protein and Rec12-dependent crossover recombination (chiasmata) in meiosis I; and a requirement for Rec12 in meiosis II.

Wallace D Sharif, Gloria G Glick, Mari K Davidson, Wayne P Wahls

Abstract read
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Article in Cell & chromosome, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

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45citing papers in PubMed
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3 · Its place in the literature

Who cites it

45 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wallace D SharifDepartment of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. WahlsWayneP@uams.edu
Gloria G Glick
Mari K Davidson
Wayne P Wahls

Funding

REGULATION OF MEIOTIC DEVELOPMENT BY MTS1-MTS2 PROTEINR01GM062244 · NIGMS · VANDERBILT UNIVERSITY · PI WAHLS, WAYNE P · 2001 to 2004
$1.0M
NIGMS NIH HHS R01 GM062244
6 · The paper itself

Abstract

backgroundIn most organisms proper reductional chromosome segregation during meiosis I is strongly correlated with the presence of crossover recombination structures (chiasmata); recombination deficient mutants lack crossovers and suffer meiosis I nondisjunction. We report that these functions are separable in the fission yeast Schizosaccharomyces pombe.

resultsIntron mapping and expression studies confirmed that Rec12 is a member of the Spo11/Top6A topoisomerase family required for the formation of meiotic dsDNA breaks and recombination. rec12-117, rec12-D15 (null), and rec12-Y98F (active site) mutants lacked most crossover recombination and chromosomes segregated abnormally to generate aneuploid meiotic products. Since S. pombe contains only three chromosome pairs, many of those aneuploid products were viable. The types of aberrant chromosome segregation were inferred from the inheritance patterns of centromere linked markers in diploid meiotic products. The rec12-117 and rec12-D15 mutants manifest segregation errors during both meiosis I and meiosis II. Remarkably, the rec12-Y98F (active site) mutant exhibited essentially normal meiosis I segregation patterns, but still exhibited meiosis II segregation errors.

conclusionsRec12 is a 345 amino acid protein required for most crossover recombination and for chiasmatic segregation of chromosomes during meiosis I. Rec12 also participates in a backup distributive (achiasmatic) system of chromosome segregation during meiosis I. In addition, catalytically-active Rec12 mediates some signal that is required for faithful equational segregation of chromosomes during meiosis II.

Identifiers

PMID12437782
PMCPMC131009

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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.