Evidence map›Paper›PMID 33745061›Full record

ReviewCurrent genetics2021

Meiotic regulation of the Ndc80 complex composition and function.

Jingxun Chen, Elçin Ünal

Open access · hybridAbstract readReview
In one paragraph

Review in Current genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Jingxun ChenDepartment of Molecular and Cell Biology, University of California, Berkeley, CA, 94720, USA.
Elçin ÜnalDepartment of Molecular and Cell Biology, University of California, Berkeley, CA, 94720, USA. elcin@berkeley.edu.ORCID http://orcid.org/0000-0002-6768-609X
University of California, Berkeley · US

Funding

ILLUMINATING CELLULAR AGING PATHWAYS THROUGH GAMETOGENESISDP2AG055946 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI UNAL, ELCIN · 2016 to 2016
$2.2M
Damon Runyon Cancer Research Foundation 35-15National Science Foundation (US) DGE-1106400NIA NIH HHS DP2 AG055946NIH HHS DP2 AG055946-01Pew Charitable Trusts 00027344
6 · The paper itself

Abstract

This review describes the current models for how the subunit abundance of the Ndc80 complex, a key kinetochore component, is regulated in budding yeast and metazoan meiosis. The past decades of kinetochore research have established the Ndc80 complex to be a key microtubule interactor and a central hub for regulating chromosome segregation. Recent studies further demonstrate that Ndc80 is the limiting kinetochore subunit that dictates the timing of kinetochore activation in budding yeast meiosis. Here, we discuss the molecular circuits that regulate Ndc80 protein synthesis and degradation in budding yeast meiosis and compare the findings with those from metazoans. We envision the regulatory principles discovered in budding yeast to be conserved in metazoans, thereby providing guidance into future investigations on kinetochore regulation in human health and disease.

Indexed as

Chromosome SegregationCytoskeletal ProteinsHumansKinetochoresMeiosisMicrotubulesNuclear ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCytoskeletal ProteinsNDC80 protein, humanNDC80 protein, S cerevisiaeNuclear ProteinsSaccharomyces cerevisiae ProteinsChromosome segregationKinetochoreLUTIMeiosisProteolysisTranscript isoformsuORF

Identifiers

PMID33745061
PMCPMC8254699
OpenAlexW3136980307

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.