Evidence map›Paper›PMID 26104357›Full record

ReviewMicrobiology spectrum2014

A Unique DNA Recombination Mechanism of the Mating/Cell-type Switching of Fission Yeasts: a Review.

Amar J S Klar, Ken Ishikawa, Sharon Moore

Open access · greenAbstract readReview
In one paragraph

Review in Microbiology spectrum, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

  1. RAD51-mediated R-loop formation acts to repair transcription-associated DNA breaks driving antigenic variation inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  2. Article
  3. Article
  4. The Fission Yeast Mating-Type Switching Motto: "One-for-Two" and "Two-for-One".Microbiology and molecular biology reviews : MMBR · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Genes · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Ten principles of heterochromatin formation and function.Nature reviews. Molecular cell biology · 2018
    Review
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Amar J S KlarNational Cancer Institute at Frederick, Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute at Frederick, P.O. Box B, Frederick, MD 21702-1201.
Ken IshikawaNational Cancer Institute at Frederick, Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute at Frederick, P.O. Box B, Frederick, MD 21702-1201.
Sharon MooreNational Cancer Institute at Frederick, Gene Regulation and Chromosome Biology Laboratory, National Cancer Institute at Frederick, P.O. Box B, Frederick, MD 21702-1201.
National Cancer Institute · USFrederick National Laboratory for Cancer Research · US

Funding

Studies on mat1 ImprintingZIABC010385 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLAR, AMAR J · 2009 to 2016
$3.6M
STUDIES ON MAT1 ON IMPRINTINGZ01BC010385 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLAR, AMAR J · 2000 to 2008
$602k
Intramural NIH HHS Z01 BC010385
6 · The paper itself

Abstract

Cells of the highly diverged Schizosaccharomyces (S.) pombe and S. japonicus fission yeasts exist in one of two sex/mating types, called P (for plus) or M (for minus), specified by which allele, M or P, resides at mat1. The fission yeasts have evolved an elegant mechanism for switching P or M information at mat1 by a programmed DNA recombination event with a copy of one of the two silent mating-type genes residing nearby in the genome. The switching process is highly cell-cycle and generation dependent such that only one of four grandchildren of a cell switches mating type. Extensive studies of fission yeast established the natural DNA strand chirality at the mat1 locus as the primary basis of asymmetric cell division. The asymmetry results from a unique site- and strand-specific epigenetic "imprint" at mat1 installed in one of the two chromatids during DNA replication. The imprint is inherited by one daughter cell, maintained for one cell cycle, and is then used for initiating recombination during mat1 replication in the following cell cycle. This mechanism of cell-type switching is considered to be unique to these two organisms, but determining the operation of such a mechanism in other organisms has not been possible for technical reasons. This review summarizes recent exciting developments in the understanding of mating-type switching in fission yeasts and extends these observations to suggest how such a DNA strand-based epigenetic mechanism of cellular differentiation could also operate in diploid organisms.

Indexed as

Genes, Mating Type, FungalRecombination, GeneticAllelesCell CycleDNA, FungalEpigenesis, GeneticGenes, FungalSchizosaccharomycesDNA, Fungal

Identifiers

PMID26104357
PMCPMC7687047
OpenAlexW2019738496

What OpenQuestion holds

Textmetadata
LicenceTDM
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.