Evidence map›Paper›PMID 26800527›Full record

ArticlePLoS genetics2016

Dynamic Sumoylation of a Conserved Transcription Corepressor Prevents Persistent Inclusion Formation during Hyperosmotic Stress.

Michelle L Oeser, Triana Amen, Cory M Nadel, Amanda I Bradley, Benjamin J Reed, Ramon D Jones, Janani Gopalan, Daniel Kaganovich, Richard G Gardner

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  7. Review
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  15. Review
  16. TORC1-dependent sumoylation of Rpc82 promotes RNA polymerase III assembly and activity.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Ubiquitin-dependent and independent roles of SUMO in proteostasis.American journal of physiology. Cell physiology · 2016
    Review
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.

Michelle L OeserMolecular and Cellular Biology Program, University of Washington, Seattle, Washington, United States of America.
Triana AmenAlexander Grass Center for Bioengineering, Hebrew University of Jerusalem, Jerusalem, Israel.
Cory M NadelDepartment of Pharmacology, University of Washington, Seattle, Washington, United States of America.
Amanda I BradleyMolecular and Cellular Biology Program, University of Washington, Seattle, Washington, United States of America.
Benjamin J ReedDepartment of Pharmacology, University of Washington, Seattle, Washington, United States of America.
Ramon D JonesDepartment of Pharmacology, University of Washington, Seattle, Washington, United States of America.
Janani GopalanDepartment of Pharmacology, University of Washington, Seattle, Washington, United States of America.
Daniel KaganovichDepartment of Cell and Developmental Biology, Alexander Silberman Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Richard G GardnerMolecular and Cellular Biology Program, University of Washington, Seattle, Washington, United States of America.

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6M
Identifying and characterizing protein quality control mechanisms in the nucleusR01AG031136 · NIA · UNIVERSITY OF WASHINGTON · PI GARDNER, RICHARD GEORGE · 2009 to 2013
$1.6M
NIA NIH HHS R01 AG031136NIGMS NIH HHS 5T32 GM007750NIGMS NIH HHS T32 GM007270NIGMS NIH HHS T32 GM007750
6 · The paper itself

Abstract

Cells are often exposed to physical or chemical stresses that can damage the structures of essential biomolecules. Stress-induced cellular damage can become deleterious if not managed appropriately. Rapid and adaptive responses to stresses are therefore crucial for cell survival. In eukaryotic cells, different stresses trigger post-translational modification of proteins with the small ubiquitin-like modifier SUMO. However, the specific regulatory roles of sumoylation in each stress response are not well understood. Here, we examined the sumoylation events that occur in budding yeast after exposure to hyperosmotic stress. We discovered by proteomic and biochemical analyses that hyperosmotic stress incurs the rapid and transient sumoylation of Cyc8 and Tup1, which together form a conserved transcription corepressor complex that regulates hundreds of genes. Gene expression and cell biological analyses revealed that sumoylation of each protein directs distinct outcomes. In particular, we discovered that Cyc8 sumoylation prevents the persistence of hyperosmotic stress-induced Cyc8-Tup1 inclusions, which involves a glutamine-rich prion domain in Cyc8. We propose that sumoylation protects against persistent inclusion formation during hyperosmotic stress, allowing optimal transcriptional function of the Cyc8-Tup1 complex.

Indexed as

ProteomicsTranscription, GeneticGene Expression Regulation, FungalOsmotic PressurePromoter Regions, GeneticRepressor ProteinsSaccharomyces cerevisiaeSumoylationRepressor Proteins

Identifiers

PMID26800527
PMCPMC4723248

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Registered trials

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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.