Evidence map›Paper›PMID 34672913›Full record

ArticleRNA biology2021

Integrated multi-omics reveals common properties underlying stress granule and P-body formation.

Christopher J Kershaw, Michael G Nelson, Jennifer Lui, Christian P Bates, Martin D Jennings, Simon J Hubbard, Mark P Ashe, Chris M Grant

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 27 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

8 authors at 1 institution in 1 country.

Christopher J KershawUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Michael G NelsonUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Jennifer LuiUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Christian P BatesUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Martin D JenningsUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Simon J HubbardUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Mark P AsheUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.
Chris M GrantUniversity of Manchester School of Biological Science, The University of Manchester Faculty of Biology Medicine and Health, Manchester, UK.ORCID 0000-0002-0616-6576
University of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K005979/1Biotechnology and Biological Sciences Research Council BB/N014049/1Biotechnology and Biological Sciences Research Council BB/P005594/1Wellcome TrustWellcome Trust 210002/Z/17/Z
6 · The paper itself

Abstract

Non-membrane-bound compartments such as P-bodies (PBs) and stress granules (SGs) play important roles in the regulation of gene expression following environmental stresses. We have systematically and quantitatively determined the protein and mRNA composition of PBs and SGs formed before and after nutrient stress. We find that high molecular weight (HMW) complexes exist prior to glucose depletion that we propose may act as seeds for further condensation of proteins forming mature PBs and SGs. We identify an enrichment of proteins with low complexity and RNA binding domains, as well as long, structured mRNAs that are poorly translated following nutrient stress. Many proteins and mRNAs are shared between PBs and SGs including several multivalent RNA binding proteins that promote condensate interactions during liquid-liquid phase separation. We uncover numerous common protein and RNA components across PBs and SGs that support a complex interaction profile during the maturation of these biological condensates. These interaction networks represent a tuneable response to stress, highlighting previously unrecognized condensate heterogeneity. These studies therefore provide an integrated and quantitative understanding of the dynamic nature of key biological condensates.

Indexed as

GenomicsProteomicsStress, PhysiologicalGene Expression ProfilingGene Expression Regulation, FungalGlucoseHumansProcessing BodiesProteomeStress GranulesYeastsGlucoseProteomeglucose depletion yeastp-bodiesRNA fateStress granulestranslational control

Identifiers

PMID34672913
PMCPMC8782181
OpenAlexW3197897436

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.