Evidence map›Paper›PMID 23993100›Full record

ArticleCell2013

S. cerevisiae chromosomes biorient via gradual resolution of syntely between S phase and anaphase.

Eugenio Marco, Jonas F Dorn, Pei-Hsin Hsu, Khuloud Jaqaman, Peter K Sorger, Gaudenz Danuser

Abstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
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  5. Article
  6. Spindle architecture constrains karyotype in budding yeast.bioRxiv : the preprint server for biology · 2024
    Article
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  8. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Eugenio MarcoDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA; Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Jonas F DornInstitute for Research in Immunology and Cancer, University of Montreal, Montreal QC H3C 3J7, Canada.
Pei-Hsin HsuDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Khuloud JaqamanDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Peter K SorgerDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Gaudenz DanuserDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: gaudenz_danuser@hms.harvard.edu.

Funding

Computation &mechanical modeling of chromosome dynamicsR01GM068956 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI DANUSER, GAUDENZ, SORGER, PETER KARL · 2003 to 2011
$3.3M
Medical Research Council MR/K015869/1NIGMS NIH HHS R01 GM068956
6 · The paper itself

Abstract

Following DNA replication, eukaryotic cells must biorient all sister chromatids prior to cohesion cleavage at anaphase. In animal cells, sister chromatids gradually biorient during prometaphase, but current models of mitosis in S. cerevisiae assume that biorientation is established shortly after S phase. This assumption is based on the observation of a bilobed distribution of yeast kinetochores early in mitosis and suggests fundamental differences between yeast mitosis and mitosis in animal cells. By applying super-resolution imaging methods, we show that yeast and animal cells share the key property of gradual and stochastic chromosome biorientation. The characteristic bilobed distribution of yeast kinetochores, hitherto considered synonymous for biorientation, arises from kinetochores in mixed attachment states to microtubules, the length of which discriminates bioriented from syntelic attachments. Our results offer a revised view of mitotic progression in S. cerevisiae that augments the relevance of mechanistic information obtained in this powerful genetic system for mammalian mitosis.

Indexed as

AnaphaseAurora KinasesChromosomes, FungalHumansIntracellular Signaling Peptides and ProteinsKinetochoresProtein Serine-Threonine KinasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsS PhaseSpindle ApparatusAurora KinasesIntracellular Signaling Peptides and ProteinsIPL1 protein, S cerevisiaeProtein Serine-Threonine KinasesSaccharomyces cerevisiae Proteins

Identifiers

PMID23993100
PMCPMC3802543

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Registered trials

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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.