Evidence map›Paper›PMID 39481633›Full record

ReviewJournal of molecular biology2024

The Hsp90 Molecular Chaperone as a Global Modifier of the Genotype-Phenotype-Fitness Map: An Evolutionary Perspective.

José Aguilar-Rodríguez, Christopher M Jakobson, Daniel F Jarosz

Abstract readReview
In one paragraph

Review in Journal of molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. AScience signaling · 2026
    Article
  2. Review
  3. Review
  4. 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

3 authors.

José Aguilar-RodríguezDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA; Department of Biology, Stanford University, Stanford, CA, USA.
Christopher M JakobsonDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
Daniel F JaroszDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, USA. Electronic address: jarosz@stanford.edu.

Funding

Discovery of protein aggregates during vertebrate aging and neurodegenerationRF1AG057334 · NIA · STANFORD UNIVERSITY · PI BRUNET, ANNE, JAROSZ, DANIEL · 2017 to 2017
$3.7M
Investigating protein phase separation and aggregation in age dependent human diseaseR01AG086495 · NIA · STANFORD UNIVERSITY · PI Daniel Jarosz · 2024 to 2026
$3.6M
Protein-based Molecular Memories in Gene Regulation, Disease, and DevelopmentDP2GM119140 · NIGMS · STANFORD UNIVERSITY · PI JAROSZ, DANIEL · 2015 to 2015
$2.4M
Mechanisms of Action of Natural Genetic VariationR01HG012366 · NHGRI · STANFORD UNIVERSITY · PI Daniel Jarosz · 2023 to 2026
$1.5M
Using self-templating proteins to spatiotemporally organize biochemistryF32GM125162 · NIGMS · STANFORD UNIVERSITY · PI JAKOBSON, CHRISTOPHER MATTHEW · 2017 to 2019
$179k
National Science Foundation NSF-MCB116762NHGRI NIH HHS R01 HG012366NIA NIH HHS R01 AG086495NIA NIH HHS RF1 AG057334NIGMS NIH HHS DP2 GM119140NIGMS NIH HHS F32 GM125162Swiss National Science Foundation
6 · The paper itself

Abstract

Global modifier genes influence the mapping of genotypes onto phenotypes and fitness through their epistatic interactions with genetic variants on a massive scale. The first such factor to be identified, Hsp90, is a highly conserved molecular chaperone that plays a central role in protein homeostasis. Hsp90 is a "hub of hubs" that chaperones proteins engaged in many key cellular and developmental regulatory networks. These clients, which are enriched in kinases, transcription factors, and E3 ubiquitin ligases, drive diverse cellular functions and are themselves highly connected. By contrast to many other hub proteins, the abundance and activity of Hsp90 changes substantially in response to shifting environmental conditions. As a result, Hsp90 modifies the functional impact of many genetic variants simultaneously in a manner that depends on environmental stress. Studies in diverse organisms suggest that this coupling between Hsp90 function and challenging environments exerts a substantial impact on what parts of the genome are visible to natural selection, expanding adaptive opportunities when most needed. In this Perspective, we explore the multifaceted role of Hsp90 as global modifier of the genotype-phenotype-fitness map as well as its implications for evolution in nature and the clinic.

Indexed as

GenotypeHSP90 Heat-Shock ProteinsPhenotypeAnimalsEpistasis, GeneticEvolution, MolecularGenetic FitnessHumansMolecular ChaperonesSelection, GeneticHSP90 Heat-Shock ProteinsMolecular Chaperonesepistasisevolvabilitymolecular chaperonesmolecular networksmutational robustness

Identifiers

PMID39481633
PMCPMC11608137

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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.