Evidence map›Paper›PMID 28459455›Full record

ArticleNature genetics2017

DNA sequence homology induces cytosine-to-thymine mutation by a heterochromatin-related pathway in Neurospora.

Eugene Gladyshev, Nancy Kleckner

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Translation of Mutant Repetitive Genomic Sequences inInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Remodeling of perturbed chromatin can initiate de novo transcriptional and post-transcriptional silencing.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Transcriptional Silencing of 35S rDNA inInternational journal of molecular sciences · 2024
    Article
  12. What lies behind the large genome ofFrontiers in fungal biology · 2024
    Article
  13. Review
  14. Review
  15. Article
  16. DNA Methyltransferases and DNA Damage.Advances in experimental medicine and biology · 2022
    Article
  17. Article
  18. Recombination-independent recognition of DNA homology for meiotic silencing inProceedings of the National Academy of Sciences of the United States of America · 2021
    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

2 authors at 1 institution in 1 country.

Eugene GladyshevDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.ORCID http://orcid.org/0000-0002-4074-4966
Nancy KlecknerDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.
Harvard University · US

Funding

MEIOTIC CHROMOSOME SYNAPSIS AND RECOMBINATION IN YEASTR01GM044794 · NIGMS · HARVARD UNIVERSITY · PI KLECKNER, NANCY E · 1990 to 2018
$13.8M
NIGMS NIH HHS R01 GM044794
6 · The paper itself

Abstract

Most eukaryotic genomes contain substantial amounts of repetitive DNA organized in the form of constitutive heterochromatin and associated with repressive epigenetic modifications, such as H3K9me3 and C5 cytosine methylation (5mC). In the fungus Neurospora crassa, H3K9me3 and 5mC are catalyzed, respectively, by a conserved SUV39 histone methyltransferase, DIM-5, and a DNMT1-like cytosine methyltransferase, DIM-2. Here we show that DIM-2 can also mediate repeat-induced point mutation (RIP) of repetitive DNA in N. crassa. We further show that DIM-2-dependent RIP requires DIM-5, HP1, and other known heterochromatin factors, implying a role for a repeat-induced heterochromatin-related process. Our previous findings suggest that the mechanism of repeat recognition for RIP involves direct interactions between homologous double-stranded DNA (dsDNA) segments. We thus now propose that, in somatic cells, homologous dsDNA-dsDNA interactions between a small number of repeat copies can nucleate a transient heterochromatic state, which, on longer repeat arrays, may lead to the formation of constitutive heterochromatin.

Indexed as

CytosinePoint MutationThymineDNA (Cytosine-5-)-MethyltransferasesDNA, Single-StrandedFungal ProteinsHeterochromatinMethylationNeurospora crassaRepetitive Sequences, Nucleic AcidSequence Homology, Nucleic AcidCytosineDNA (Cytosine-5-)-MethyltransferasesDNA, Single-StrandedFungal ProteinsHeterochromatinThymine

Identifiers

PMID28459455
PMCPMC5474309
OpenAlexW2611365178

What OpenQuestion holds

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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.