Evidence map›Paper›PMID 29346421›Full record

ArticlePloS one2018

The absence of specific yeast heat-shock proteins leads to abnormal aggregation and compromised autophagic clearance of mutant Huntingtin proteins.

Ryan Higgins, Marie-Helene Kabbaj, Alexa Hatcher, Yanchang Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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  7. International journal of molecular sciences · 2022
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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

4 authors at 1 institution in 1 country.

Ryan HigginsDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, Florida, United States of America.
Marie-Helene KabbajDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, Florida, United States of America.
Alexa HatcherCollege of Nursing, Florida State University, Tallahassee, Florida, United States of America.
Yanchang WangDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, Florida, United States of America.ORCID 0000-0001-6782-0570
Florida State University · US

Funding

The Initiation of DNA Replication in EukaryotesR01GM121786 · NIGMS · FLORIDA STATE UNIVERSITY · PI WANG, YANCHANG · 2017 to 2020
$1.2M
Investigate the molecular mechanism that ensures chromosome bipolar attachmentR01GM102115 · NIGMS · FLORIDA STATE UNIVERSITY · PI WANG, YANCHANG · 2013 to 2016
$1.0M
NIGMS NIH HHS R01 GM102115NIGMS NIH HHS R01 GM121786NIH HHS RO1GM102115
6 · The paper itself

Abstract

The functionality of a protein depends on its correct folding, but newly synthesized proteins are susceptible to aberrant folding and aggregation. Heat shock proteins (HSPs) function as molecular chaperones that aid in protein folding and the degradation of misfolded proteins. Trinucleotide (CAG) repeat expansion in the Huntingtin gene (HTT) results in the expression of misfolded Huntingtin protein (Htt), which contributes to the development of Huntington's disease. We previously found that the degradation of mutated Htt with polyQ expansion (Htt103QP) depends on both ubiquitin proteasome system and autophagy. However, the role of heat shock proteins in the clearance of mutated Htt remains poorly understood. Here, we report that cytosolic Hsp70 (Ssa family), its nucleotide exchange factors (Sse1 and Fes1), and a Hsp40 co-chaperone (Ydj1) are required for inclusion body formation of Htt103QP proteins and their clearance via autophagy. Extended induction of Htt103QP-GFP leads to the formation of a single inclusion body in wild-type yeast cells, but mutant cells lacking these HSPs exhibit increased number of Htt103QP aggregates. Most notably, we detected more aggregated forms of Htt103QP in sse1Δ mutant cells using an agarose gel assay. Increased protein aggregates are also observed in these HSP mutants even in the absence Htt103QP overexpression. Importantly, these HSPs are required for autophagy-mediated Htt103QP clearance, but are less critical for proteasome-dependent degradation. These findings suggest a chaperone network that facilitates inclusion body formation of misfolded proteins and the subsequent autophagic clearance.

Indexed as

AutophagyMutationHeat-Shock ProteinsHuntingtin ProteinSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTrinucleotide RepeatsHeat-Shock ProteinsHuntingtin ProteinSaccharomyces cerevisiae Proteins

Identifiers

PMID29346421
PMCPMC5773196
OpenAlexW2793466414

What Socratic 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 Socratic graph.