Evidence map›Paper›PMID 31076383›Full record

ArticleG3 (Bethesda, Md.)2019

Synthetic Physical Interactions with the Yeast Centrosome.

Rowan S M Howell, Attila Csikász-Nagy, Peter H Thorpe

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 9 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

3 authors at 3 institutions in 3 countries.

Rowan S M HowellThe Francis Crick Institute, London, NW1 1AT UK.ORCID 0000-0002-2479-180X
Attila Csikász-NagyRandall Division of Cell and Molecular Biophysics, King's College, London, SE1 1UL UK p.thorpe@qmul.ac.uk attila.csikasz-nagy@kcl.ac.uk.ORCID 0000-0002-2919-5601
Peter H ThorpeSchool of Biological and Chemical Sciences, Queen Mary University, London, E1 4NS UK p.thorpe@qmul.ac.uk attila.csikasz-nagy@kcl.ac.uk.ORCID 0000-0003-1649-6816
Institute of Molecular Biology and Biophysics · RUKing's College London · GBQueen Mary University of London · GB

Funding

Cancer Research UK FC001003Medical Research Council FC001003Medical Research Council MC_UP_A252_1027Wellcome Trust FC001003
6 · The paper itself

Abstract

The yeast centrosome or Spindle Pole Body (SPB) is an organelle situated in the nuclear membrane, where it nucleates spindle microtubules and acts as a signaling hub. Various studies have explored the effects of forcing individual proteins to interact with the yeast SPB, however no systematic study has been performed. We used synthetic physical interactions to detect proteins that inhibit growth when forced to associate with the SPB. We found the SPB to be especially sensitive to relocalization, necessitating a novel data analysis approach. This novel analysis of SPI screening data shows that regions of the cell are locally more sensitive to forced relocalization than previously thought. Furthermore, we found a set of associations that result in elevated SPB number and, in some cases, multi-polar spindles. Since hyper-proliferation of centrosomes is a hallmark of cancer cells, these associations point the way for the use of yeast models in the study of spindle formation and chromosome segregation in cancer.

Indexed as

BiomarkersCentrosomeComputational BiologyFungal ProteinsGene OntologyModels, BiologicalProtein Interaction MappingSpindle ApparatusSpindle Pole BodiesYeastsBiomarkersFungal Proteinscentrosomeempirical BayeslocalizationSpindle Pole Body

Identifiers

PMID31076383
PMCPMC6643875
OpenAlexW2944660306

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.