Evidence map›Paper›PMID 16260499›Full record

ArticleThe Journal of cell biology2005

Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I.

Nadine K Kolas, Anton Svetlanov, Michelle L Lenzi, Frank P Macaluso, Steven M Lipkin, R Michael Liskay, John Greally, Winfried Edelmann, Paula E Cohen

Abstract read
In one paragraph

Article in The Journal of cell biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
–field-weighted citation impact
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

88 citing papers in PubMed.

  1. Article
  2. Article
  3. Meiotic prophase I disruption as a strategy for nonhormonal male contraception using small-molecule inhibitor JQ1.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Mouse X-linked microRNA cluster regulates the meiotic checkpoint andProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
  8. RNF212B E3 ligase is essential for crossover designation and maturation during male and female meiosis in the mouse.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Achiasmatic meiosis in the unisexual Amazon molly, Poecilia formosa.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Article
  18. Article
  19. A Homozygous Loss-of-Function Mutation inInternational journal of molecular sciences · 2022
    Article
  20. Article

28 more citing papers are in PubMed but not listed here.

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

9 authors.

Nadine K KolasDepartment of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Anton Svetlanov
Michelle L Lenzi
Frank P Macaluso
Steven M Lipkin
R Michael Liskay
John Greally
Winfried Edelmann
Paula E Cohen

Funding

TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
The MLH1-MLH3 Heterodimer in Mammalian Meiotic Recombination and GameogenesisR01HD041012 · NICHD · YESHIVA UNIVERSITY · PI Paula Elaine Cohen · 2003 to 2026
$7.9M
DNA MISMATCH REPAIR AND CANCER IN MURINE MODELSR01CA076329 · NCI · YESHIVA UNIVERSITY · PI EDELMANN, WINFRIED · 1998 to 2017
$6.9M
NCI NIH HHS R01 CA076329NCI NIH HHS R01CA76329NICHD NIH HHS R01 HD041012NICHD NIH HHS R01HD41012-01NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32 GM 07491
6 · The paper itself

Abstract

Mammalian MutL homologues function in DNA mismatch repair (MMR) after replication errors and in meiotic recombination. Both functions are initiated by a heterodimer of MutS homologues specific to either MMR (MSH2-MSH3 or MSH2-MSH6) or crossing over (MSH4-MSH5). Mutations of three of the four MutL homologues (Mlh1, Mlh3, and Pms2) result in meiotic defects. We show herein that two distinct complexes involving MLH3 are formed during murine meiosis. The first is a stable association between MLH3 and MLH1 and is involved in promoting crossing over in conjunction with MSH4-MSH5. The second complex involves MLH3 together with MSH2-MSH3 and localizes to repetitive sequences at centromeres and the Y chromosome. This complex is up-regulated in Pms2-/- males, but not females, providing an explanation for the sexual dimorphism seen in Pms2-/- mice. The association of MLH3 with repetitive DNA sequences is coincident with MSH2-MSH3 and is decreased in Msh2-/- and Msh3-/- mice, suggesting a novel role for the MMR family in the maintenance of repeat unit integrity during mammalian meiosis.

Indexed as

Meiotic Prophase IAdaptor Proteins, Signal TransducingAdenosine TriphosphatasesAnimalsCarrier ProteinsCell Cycle ProteinsCentromereDNA-Binding ProteinsDNA Repair EnzymesMaleMeiosisMiceMice, KnockoutMicroscopy, ImmunoelectronMismatch Repair Endonuclease PMS2MutL Protein Homolog 1Adaptor Proteins, Signal TransducingAdenosine TriphosphatasesCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsDNA Repair EnzymesMismatch Repair Endonuclease PMS2Mlh1 protein, mouseMlh3 protein, mouseMsh2 protein, mouseMsh3 protein, mouseMsh4 protein, mouseMsh5 protein, mouseMutL Protein Homolog 1MutL ProteinsMutS Homolog 2 ProteinMutS Homolog 3 ProteinNuclear ProteinsPms2 protein, mouseProteins

Identifiers

PMID16260499
PMCPMC2171243

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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.