Evidence map›Paper›PMID 28841138›Full record

ArticleeLife2017

Aneuploidy as a cause of impaired chromatin silencing and mating-type specification in budding yeast.

Wahid A Mulla, Chris W Seidel, Jin Zhu, Hung-Ji Tsai, Sarah E Smith, Pushpendra Singh, William D Bradford, Scott McCroskey, Anjali R Nelliat, Juliana Conkright and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Effects of aneuploidy on cell behaviour and function.Nature reviews. Molecular cell biology · 2022
    Review
  5. Review
  6. Review
  7. Article
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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

14 authors at 2 institutions in 1 country.

Wahid A MullaDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.ORCID http://orcid.org/0000-0003-3356-3902
Chris W SeidelStowers Institute for Medical Research, Missouri, United States.
Jin ZhuDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.
Hung-Ji TsaiDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.
Sarah E SmithStowers Institute for Medical Research, Missouri, United States.
Pushpendra SinghDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.
William D BradfordStowers Institute for Medical Research, Missouri, United States.
Scott McCroskeyStowers Institute for Medical Research, Missouri, United States.
Anjali R NelliatDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.
Juliana ConkrightStowers Institute for Medical Research, Missouri, United States.
Allison PeakStowers Institute for Medical Research, Missouri, United States.
Kathryn E MalanowskiStowers Institute for Medical Research, Missouri, United States.
Anoja G PereraStowers Institute for Medical Research, Missouri, United States.
Rong LiDepartment of Cell Biology, Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, United States.ORCID http://orcid.org/0000-0002-0540-6566
Stowers Institute for Medical Research · USJohns Hopkins University · US

Funding

Mechanisms of cell polarization in yeastR01GM057063 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI LI, RONG · 1998 to 2015
$5.3M
Cellular dynamics in division, motility and evolutionary adaptationR35GM118172 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LI, RONG · 2016 to 2019
$2.8M
NIGMS NIH HHS R01 GM057063NIGMS NIH HHS R35 GM118172
6 · The paper itself

Abstract

Aneuploidy and epigenetic alterations have long been associated with carcinogenesis, but it was unknown whether aneuploidy could disrupt the epigenetic states required for cellular differentiation. In this study, we found that ~3% of random aneuploid karyotypes in yeast disrupt the stable inheritance of silenced chromatin during cell proliferation. Karyotype analysis revealed that this phenotype was significantly correlated with gains of chromosomes III and X. Chromosome X disomy alone was sufficient to disrupt chromatin silencing and yeast mating-type identity as indicated by a lack of growth response to pheromone. The silencing defect was not limited to cryptic mating type loci and was associated with broad changes in histone modifications and chromatin localization of Sir2 histone deacetylase. The chromatin-silencing defect of disome X can be partially recapitulated by an extra copy of several genes on chromosome X. These results suggest that aneuploidy can directly cause epigenetic instability and disrupt cellular differentiation.

Indexed as

AneuploidyEpigenesis, GeneticGene Expression Regulation, FungalGenes, Mating Type, FungalCell CycleChromatinSaccharomycetalesChromatinaneuploidycell biologycellular differentiationchromatin silencingchromosomesepigenetic instabilitygenesS. cerevisiae

Identifiers

PMID28841138
PMCPMC5779231
OpenAlexW2746369448

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.