Evidence map›Paper›PMID 40884183›Full record

ArticleGenetics2025

Genotype-by-environment interactions shape ubiquitin-proteasome system activity.

Randi R Avery, Mahlon A Collins, Frank W Albert

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Randi R AveryDepartment of Genetics, Cell Biology, and Development, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.ORCID 0000-0002-1490-660X
Mahlon A CollinsDepartment of Genetics, Cell Biology, and Development, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.
Frank W AlbertDepartment of Genetics, Cell Biology, and Development, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.ORCID 0000-0002-1380-8063

Funding

Genomic approaches for dissecting regulatory variationR35GM124676 · NIGMS · UNIVERSITY OF MINNESOTA · PI Frank Wolfgang Albert · 2017 to 2026
$4.6M
NIGMS NIH HHS R35 GM124676NIH HHS R35GM124676
6 · The paper itself

Abstract

In genotype-by-environment interactions (GxE), the effect of a genetic variant on a trait depends on the environment. GxE influences numerous organismal traits. However, we have limited understanding of how GxE shapes molecular processes. Here, we characterized how GxE shapes protein degradation, an essential molecular process that affects cellular and organismal physiology. Using 2 isolates of the yeast Saccharomyces cerevisiae, we profiled GxE in the ubiquitin-proteasome system (UPS), the primary protein degradation system in eukaryotes. By measuring UPS degradation activity toward 6 substrates that engage multiple distinct UPS pathways across 8 diverse environments, we discovered extensive GxE in the genetics of the UPS. The effects of all environments, including environments previously reported to affect UPS activity, differed between isolates and UPS substrates. To identify genomic regions underlying GxE for UPS activity, we mapped genetic influences on all our environment-UPS substrate combinations. Hundreds of locus effects varied depending on the environment. Most of these corresponded to loci that were present in one environment but not another ("presence/absence" GxE), while a smaller number of loci had opposing effects in different environments ("sign change" GxE). The number, genomic location, and type of GxE (presence/absence or sign change) of loci exhibiting GxE varied across UPS substrates. Loci exhibiting GxE were clustered at genomic regions that contain core UPS genes and at regions containing variation that affects the expression of thousands of genes, suggesting indirect contributions to UPS activity. Our results reveal complex interactions between the environment and the genetics of protein degradation.

Indexed as

Gene-Environment InteractionProteasome Endopeptidase ComplexSaccharomyces cerevisiaeUbiquitinGenotypeProteolysisSaccharomyces cerevisiae ProteinsProteasome Endopeptidase ComplexSaccharomyces cerevisiae ProteinsUbiquitingenotype-by-environment interactionsquantitative trait lociSaccharomyces cerevisiaeubiquitin-proteasome system

Identifiers

PMID40884183
PMCPMC12606439

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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.