Evidence map›Paper›PMID 28906249›Full record

ArticleeLife2017

Kinetochore inactivation by expression of a repressive mRNA.

Jingxun Chen, Amy Tresenrider, Minghao Chia, David T McSwiggen, Gianpiero Spedale, Victoria Jorgensen, Hanna Liao, Folkert Jacobus van Werven, Elçin Ünal

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 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Repression ofbioRxiv : the preprint server for biology · 2024
    Article
  10. Alternative splicing generates isoform diversity inEndocrine oncology (Bristol, England) · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Functional Meaning of 5'UTR in Protein-Coding Genes.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Jingxun Chen *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Amy Tresenrider *Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Minghao ChiaThe Francis Crick Institute, London, United Kingdom.
David T McSwiggenDepartment of Molecular and Cell Biology, Li Ka Shing Center, University of California, Berkeley, Berkeley, United States.
Gianpiero SpedaleThe Francis Crick Institute, London, United Kingdom.
Victoria JorgensenDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Hanna LiaoDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Folkert Jacobus van WervenThe Francis Crick Institute, London, United Kingdom.ORCID http://orcid.org/0000-0002-6685-2084
Elçin ÜnalDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.ORCID http://orcid.org/0000-0002-6768-609X
University of California, Berkeley · USThe Francis Crick Institute · GB

Funding

THE MOLECULAR BASIS OF CELL FUNCTIONT32GM007232 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BILDER, DAVID, UNAL, ELCIN · 1985 to 2022
$36.4M
ILLUMINATING CELLULAR AGING PATHWAYS THROUGH GAMETOGENESISDP2AG055946 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI UNAL, ELCIN · 2016 to 2016
$2.2M
Cancer Research UK 17576Cancer Research UK FC001203Medical Research Council FC001203NIA NIH HHS DP2 AG055946NIGMS NIH HHS T32 GM007232Wellcome Trust FC001203
6 · The paper itself

Abstract

Differentiation programs such as meiosis depend on extensive gene regulation to mediate cellular morphogenesis. Meiosis requires transient removal of the outer kinetochore, the complex that connects microtubules to chromosomes. How the meiotic gene expression program temporally restricts kinetochore function is unknown. We discovered that in budding yeast, kinetochore inactivation occurs by reducing the abundance of a limiting subunit, Ndc80. Furthermore, we uncovered an integrated mechanism that acts at the transcriptional and translational level to repress

Indexed as

Gene Expression Regulation, FungalMeiosisKinetochoresNuclear ProteinsProtein BiosynthesisRNA IsoformsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription, GeneticNDC80 protein, S cerevisiaeNuclear ProteinsRNA IsoformsSaccharomyces cerevisiae Proteinsbudding yeastchromosomesgene regulationgeneskinetochoremeiosisS. cerevisiaetranscriptionuORF translation

Identifiers

PMID28906249
PMCPMC5655150
OpenAlexW2754798708

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.