Evidence map›Paper›PMID 25135640›Full record

ArticleThe Journal of biological chemistry2014

Structural maintenance of chromosome (SMC) proteins link microtubule stability to genome integrity.

Guillaume Laflamme, Thierry Tremblay-Boudreault, Marc-André Roy, Parker Andersen, Éric Bonneil, Kaleem Atchia, Pierre Thibault, Damien D'Amours, Benjamin H Kwok

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Histone variant H2B.Z acetylation is necessary for maintenance ofbioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Frontiers in plant science · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
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

9 authors at 1 institution in 1 country.

Guillaume LaflammeFrom the Chemical Biology of Cell Division Laboratory, the Laboratory of Cell Cycle Regulation and Chromosome Structure, and.
Thierry Tremblay-BoudreaultFrom the Chemical Biology of Cell Division Laboratory.
Marc-André Roythe Laboratory of Cell Cycle Regulation and Chromosome Structure, and.
Parker AndersenFrom the Chemical Biology of Cell Division Laboratory.
Éric Bonneilthe Laboratory of Proteomics and Bioanalytical Mass Spectrometry, Institute for Research in Immunology and Cancer, and.
Kaleem AtchiaFrom the Chemical Biology of Cell Division Laboratory.
Pierre Thibaultthe Laboratory of Proteomics and Bioanalytical Mass Spectrometry, Institute for Research in Immunology and Cancer, and the Departments of Chemistry.
Damien D'Amoursthe Laboratory of Cell Cycle Regulation and Chromosome Structure, and Pathology and Cellular Biology, and damien.damours@umontreal.ca.
Benjamin H KwokFrom the Chemical Biology of Cell Division Laboratory, Medicine, Université de Montréal, Station Centre-Ville, Montréal, Québec H3C 3J7, Canada benjamin.kwok@umontreal.ca.
Université de Montréal · CA

Funding

Canadian Institutes of Health Research MOP-82912Canadian Institutes of Health Research MOP-97928
6 · The paper itself

Abstract

Structural maintenance of chromosome (SMC) proteins are key organizers of chromosome architecture and are essential for genome integrity. They act by binding to chromatin and connecting distinct parts of chromosomes together. Interestingly, their potential role in providing connections between chromatin and the mitotic spindle has not been explored. Here, we show that yeast SMC proteins bind directly to microtubules and can provide a functional link between microtubules and DNA. We mapped the microtubule-binding region of Smc5 and generated a mutant with impaired microtubule binding activity. This mutant is viable in yeast but exhibited a cold-specific conditional lethality associated with mitotic arrest, aberrant spindle structures, and chromosome segregation defects. In an in vitro reconstitution assay, this Smc5 mutant also showed a compromised ability to protect microtubules from cold-induced depolymerization. Collectively, these findings demonstrate that SMC proteins can bind to and stabilize microtubules and that SMC-microtubule interactions are essential to establish a robust system to maintain genome integrity.

Indexed as

Genomic InstabilityBinding SitesCell Cycle ProteinsGenome, FungalMicrotubulesProtein BindingProtein StabilitySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCell Cycle ProteinsSaccharomyces cerevisiae ProteinsSMC5 protein, S cerevisiaeCell DivisionChromosomesMicrotubuleMitosisMitotic SpindleSMC Proteins

Identifiers

PMID25135640
PMCPMC4183782
OpenAlexW2010098108

What OpenQuestion holds

Textmetadata
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.