Evidence map›Paper›PMID 24918601›Full record

ArticlePloS one2014

Unidirectional P-body transport during the yeast cell cycle.

Cecilia Garmendia-Torres, Alexander Skupin, Sean A Michael, Pekka Ruusuvuori, Nathan J Kuwada, Didier Falconnet, Gregory A Cary, Carl Hansen, Paul A Wiggins, Aimée M Dudley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-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

9 citing papers in PubMed, 17 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

10 authors at 6 institutions in 5 countries.

Cecilia Garmendia-TorresInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Alexander SkupinLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg; National Center for Microscopy and Imaging Research, University of California San Diego, La Jolla, California, United States of America.
Sean A MichaelInstitute for Systems Biology, Seattle, Washington, United States of America.
Pekka RuusuvuoriTampere University of Technology, Pori, Finland; BioMediTech, University of Tampere, Tampere, Finland.
Nathan J KuwadaPhysics and Bioengineering, University of Washington, Seattle, Washington, United States of America.
Didier FalconnetCentre for High-Throughput Biology, Department of Physics and Astronomy, University of British Columbia, Vancouver, British Columbia, Canada.
Gregory A CaryInstitute for Systems Biology, Seattle, Washington, United States of America; Molecular and Cellular Biology Program, University of Washington, Seattle, Washington, United States of America.
Carl HansenCentre for High-Throughput Biology, Department of Physics and Astronomy, University of British Columbia, Vancouver, British Columbia, Canada.
Paul A WigginsPhysics and Bioengineering, University of Washington, Seattle, Washington, United States of America.
Aimée M DudleyMolecular and Cellular Biology Program, University of Washington, Seattle, Washington, United States of America; Pacific Northwest Diabetes Research Institute, Seattle, Washington, United States of America.
University of Washington · USInstitute for Systems Biology · USUniversity of British Columbia · CAInstitut de génétique et de biologie moléculaire et cellulaire · FRTampere University · FIUniversity of California San Diego · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
NIGMS NIH HHS P50 GM076547
6 · The paper itself

Abstract

P-bodies belong to a large family of RNA granules that are associated with post-transcriptional gene regulation, conserved from yeast to mammals, and influence biological processes ranging from germ cell development to neuronal plasticity. RNA granules can also transport RNAs to specific locations. Germ granules transport maternal RNAs to the embryo, and neuronal granules transport RNAs long distances to the synaptic dendrites. Here we combine microfluidic-based fluorescent microscopy of single cells and automated image analysis to follow p-body dynamics during cell division in yeast. Our results demonstrate that these highly dynamic granules undergo a unidirectional transport from the mother to the daughter cell during mitosis as well as a constrained "hovering" near the bud site half an hour before the bud is observable. Both behaviors are dependent on the Myo4p/She2p RNA transport machinery. Furthermore, single cell analysis of cell size suggests that PBs play an important role in daughter cell growth under nutrient limiting conditions.

Indexed as

Biological TransportCell CycleCytoplasmic GranulesMicrofluidicsSaccharomyces cerevisiae

Identifiers

PMID24918601
PMCPMC4053424
OpenAlexW2022336048

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.