Evidence map›Paper›PMID 32155147›Full record

ArticlePLoS biology2020

Evolutionary repair: Changes in multiple functional modules allow meiotic cohesin to support mitosis.

Yu-Ying Phoebe Hsieh, Vasso Makrantoni, Daniel Robertson, Adèle L Marston, Andrew W Murray

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Cohesin ring gates are specialized for meiotic cell division.Journal of molecular cell biology · 2025
    Article
  5. Experimental evolution for cell biology.Trends in cell biology · 2023
    Review
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  7. Article
  8. Article
  9. Article
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  11. Review
  12. 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

5 authors at 2 institutions in 2 countries.

Yu-Ying Phoebe HsiehDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, United States of America.ORCID 0000-0001-8500-3873
Vasso MakrantoniThe Wellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0003-0668-6157
Daniel RobertsonThe Wellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0003-3894-7200
Adèle L MarstonThe Wellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-3596-9407
Andrew W MurrayDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-0868-6604
Wellcome Centre for Cell Biology · GBHarvard University · US

Funding

FEEDBACK CONTROL OF THE CELL CYCLER01GM043987 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MURRAY, ANDREW W · 1990 to 2023
$6.4M
NIGMS NIH HHS R01 GM043987Wellcome Trust 107827Wellcome Trust 203149
6 · The paper itself

Abstract

The role of proteins often changes during evolution, but we do not know how cells adapt when a protein is asked to participate in a different biological function. We forced the budding yeast, Saccharomyces cerevisiae, to use the meiosis-specific kleisin, recombination 8 (Rec8), during the mitotic cell cycle, instead of its paralog, Scc1. This perturbation impairs sister chromosome linkage, advances the timing of genome replication, and reduces reproductive fitness by 45%. We evolved 15 parallel populations for 1,750 generations, substantially increasing their fitness, and analyzed the genotypes and phenotypes of the evolved cells. Only one population contained a mutation in Rec8, but many populations had mutations in the transcriptional mediator complex, cohesin-related genes, and cell cycle regulators that induce S phase. These mutations improve sister chromosome cohesion and delay genome replication in Rec8-expressing cells. We conclude that changes in known and novel partners allow cells to use an existing protein to participate in new biological functions.

Indexed as

MitosisAdaptation, BiologicalCell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosomes, FungalCohesinsDirected Molecular EvolutionEvolution, MolecularGenome, FungalMeiosisMutationReplication OriginSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSister Chromatid ExchangeCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsMCD1 protein, S cerevisiaeREC8 protein, S cerevisiaeSaccharomyces cerevisiae Proteins

Identifiers

PMID32155147
PMCPMC7138332
OpenAlexW3011321335

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.