Evidence map›Paper›PMID 19687257›Full record

ArticleThe Journal of cell biology2009

Myosin-driven peroxisome partitioning in S. cerevisiae.

Andrei Fagarasanu, Fred D Mast, Barbara Knoblach, Yui Jin, Matthew J Brunner, Michael R Logan, J N Mark Glover, Gary A Eitzen, John D Aitchison, Lois S Weisman and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.5field-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

43 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Regulatory Mechanism of Peroxisome Number Reduction Caused byJournal of fungi (Basel, Switzerland) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
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  16. Review
  17. 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

11 authors at 3 institutions in 2 countries.

Andrei FagarasanuDepartment of Cell Biology and 2 Department of Biochemistry, University of Alberta, Edmonton, Alberta T6G2H7, Canada.
Fred D Mast
Barbara Knoblach
Yui Jin
Matthew J Brunner
Michael R Logan
J N Mark Glover
Gary A Eitzen
John D Aitchison
Lois S Weisman
Richard A Rachubinski
University of Alberta · CAUniversity of Michigan–Ann Arbor · USInstitute for Systems Biology · US

Funding

Regulation of myosin V interaction with cargo-Equipment SupplementR01GM062261 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Lois S Weisman · 2001 to 2026
$5.8M
Oleate-responsive gene regulatory networks governing peroxisome proliferationR01GM075152 · NIGMS · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI AITCHISON, JOHN D. · 2008 to 2011
$1.9M
NIGMS NIH HHS R01 GM062261NIGMS NIH HHS R01 GM075152NIGMS NIH HHS R01-GM62261NIGMS NIH HHS R01-GM75152
6 · The paper itself

Abstract

In Saccharomyces cerevisiae, the class V myosin motor Myo2p propels the movement of most organelles. We recently identified Inp2p as the peroxisome-specific receptor for Myo2p. In this study, we delineate the region of Myo2p devoted to binding peroxisomes. Using mutants of Myo2p specifically impaired in peroxisome binding, we dissect cell cycle-dependent and peroxisome partitioning-dependent mechanisms of Inp2p regulation. We find that although total Inp2p levels oscillate with the cell cycle, Inp2p levels on individual peroxisomes are controlled by peroxisome inheritance, as Inp2p aberrantly accumulates and decorates all peroxisomes in mother cells when peroxisome partitioning is abolished. We also find that Inp2p is a phosphoprotein whose level of phosphorylation is coupled to the cell cycle irrespective of peroxisome positioning in the cell. Our findings demonstrate that both organelle positioning and cell cycle progression control the levels of organelle-specific receptors for molecular motors to ultimately achieve an equidistribution of compartments between mother and daughter cells.

Indexed as

Saccharomyces cerevisiaeCell CycleMembrane ProteinsMitochondriaModels, MolecularMolecular StructureMyosin Heavy ChainsMyosin Type VPeroxisomesPoint MutationProtein Processing, Post-TranslationalProtein Structure, TertiaryReceptors, Cytoplasmic and NuclearRecombinant Fusion ProteinsSaccharomyces cerevisiae ProteinsTwo-Hybrid System TechniquesINP2 protein, S cerevisiaeMembrane ProteinsMYO2 protein, S cerevisiaeMyosin Heavy ChainsMyosin Type VReceptors, Cytoplasmic and NuclearRecombinant Fusion ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID19687257
PMCPMC2733749
OpenAlexW2106281283

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.