Evidence map›Paper›PMID 30095066›Full record

ArticleeLife2018

Efficient analysis of mammalian polysomes in cells and tissues using Ribo Mega-SEC.

Harunori Yoshikawa, Mark Larance, Dylan J Harney, Ramasubramanian Sundaramoorthy, Tony Ly, Tom Owen-Hughes, Angus I Lamond

Abstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  8. Calmodulin Triggers Activity-Dependent rRNA Biogenesis via Interaction with DDX21.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  9. Dynamic changes in RNA mCellular and molecular life sciences : CMLS · 2024
    Article
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  16. Length-Dependent Translation Efficiency of ER-Destined Proteins.Current issues in molecular biology · 2023
    Article
  17. Overexpression of VIRMA confers vulnerability to breast cancers via the mCellular and molecular life sciences : CMLS · 2023
    Article
  18. 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

7 authors.

Harunori Yoshikawa *Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.ORCID 0000-0003-3793-6219
Mark Larance *Centre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Dylan J HarneyCharles Perkins Centre, School of Life and Environmental Sciences, University of Sydney, Sydney, Australia.
Ramasubramanian SundaramoorthyCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Tony LyCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.ORCID 0000-0002-8650-5215
Tom Owen-HughesCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.ORCID 0000-0002-0618-8185
Angus I LamondCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, Dundee, United Kingdom.ORCID 0000-0001-6204-6045

Funding

Cancer Institute NSW Future Research Leader fellowshipH2020 Marie Skłodowska-Curie Actions Individual Fellowship 657087Naito Foundation Grant for Overseas 2013-413National Health and Medical Research Council Project Grant GNT1120475Royal Society of Edinburgh Personal Research FellowshipScottish Government Personal Research FellowshipUehara Memorial Foundation Postdoctoral Fellowship 201430061Wellcome 073980/Z/03/ZWellcome 098503/E/12/ZWellcome 105024/Z/14/ZWellcome Sir Henry Dale Fellowship 206211/Z/17/ZWellcome Strategic Award 097945/B/11/ZWellcome Trust
6 · The paper itself

Abstract

We describe Ribo Mega-SEC, a powerful approach for the separation and biochemical analysis of mammalian polysomes and ribosomal subunits using Size Exclusion Chromatography and uHPLC. Using extracts from either cells, or tissues, polysomes can be separated within 15 min from sample injection to fraction collection. Ribo Mega-SEC shows translating ribosomes exist predominantly in polysome complexes in human cell lines and mouse liver tissue. Changes in polysomes are easily quantified between treatments, such as the cellular response to amino acid starvation. Ribo Mega-SEC is shown to provide an efficient, convenient and highly reproducible method for studying functional translation complexes. We show that Ribo Mega-SEC is readily combined with high-throughput MS-based proteomics to characterize proteins associated with polysomes and ribosomal subunits. It also facilitates isolation of complexes for electron microscopy and structural studies.

Indexed as

Protein BiosynthesisAmino AcidsAnimalsCell LineChromatography, High Pressure LiquidHumansMicePolyribosomesProteomicsRibosomesAmino Acidsbiochemistrychemical biologyhumanmammalian cells/ tissuesmousemouse liver tissueMS-based proteomicspolysome profileribosomesize exclusion chromatography (SEC)

Identifiers

PMID30095066
PMCPMC6086667

What OpenQuestion holds

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LicenceCC BY
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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.