Evidence map›Paper›PMID 39235107›Full record

ArticleMolecular biology and evolution2024

Patterns of Fitness and Gene Expression Epistasis Generated by Beneficial Mutations in the rho and rpoB Genes of Escherichia coli during High-Temperature Adaptation.

Andrea González-González, Tiffany N Batarseh, Alejandra Rodríguez-Verdugo, Brandon S Gaut

Abstract read
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Article in Molecular biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Andrea González-GonzálezDepartment of Ecology and Evolutionary Biology, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-3161-1555
Tiffany N BatarsehDepartment of Ecology and Evolutionary Biology, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-2271-0156
Alejandra Rodríguez-VerdugoDepartment of Ecology and Evolutionary Biology, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-2048-129X
Brandon S GautDepartment of Ecology and Evolutionary Biology, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-1334-5556

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
PacBio RS Single Molecule, Real-Time (SMRT) DNA SequencerS10OD010794 · OD · UNIVERSITY OF CALIFORNIA-IRVINE · PI SANDMEYER, SUZANNE · 2012 to 2012
$600k
High-Throughput DNA SequencerS10OD021718 · OD · UNIVERSITY OF CALIFORNIA-IRVINE · PI SANDMEYER, SUZANNE · 2016 to 2016
$600k
High Throughput DNA SequencerS10RR025496 · NCRR · UNIVERSITY OF CALIFORNIA-IRVINE · PI SANDMEYER, SUZANNE · 2009 to 2009
$500k
Cancer Center Support CA-62203Consejo Nacional de Ciencia y TecnologíaNational Science Foundation DEB-0748903National Science Foundation Postdoctoral Research Fellowship in Biology #2209111NCI NIH HHS P30 CA062203NCRR NIH HHS S10 RR025496NIH HHS 1S10RR025496-01NIH HHS S10 OD010794NIH HHS S10 OD021718University of California Institute for Mexico and the United StatesUniversity of California, Irvine
6 · The paper itself

Abstract

Epistasis is caused by genetic interactions among mutations that affect fitness. To characterize properties and potential mechanisms of epistasis, we engineered eight double mutants that combined mutations from the rho and rpoB genes of Escherichia coli. The two genes encode essential functions for transcription, and the mutations in each gene were chosen because they were beneficial for adaptation to thermal stress (42.2 °C). The double mutants exhibited patterns of fitness epistasis that included diminishing returns epistasis at 42.2 °C, stronger diminishing returns between mutations with larger beneficial effects and both negative and positive (sign) epistasis across environments (20.0 °C and 37.0 °C). By assessing gene expression between single and double mutants, we detected hundreds of genes with gene expression epistasis. Previous work postulated that highly connected hub genes in coexpression networks have low epistasis, but we found the opposite: hub genes had high epistasis values in both coexpression and protein-protein interaction networks. We hypothesized that elevated epistasis in hub genes reflected that they were enriched for targets of Rho termination but that was not the case. Altogether, gene expression and coexpression analyses revealed that thermal adaptation occurred in modules, through modulation of ribonucleotide biosynthetic processes and ribosome assembly, the attenuation of expression in genes related to heat shock and stress responses, and with an overall trend toward restoring gene expression toward the unstressed state.

Indexed as

DNA-Directed RNA PolymerasesEpistasis, GeneticEscherichia coliEscherichia coli ProteinsGenetic FitnessMutationAdaptation, PhysiologicalHot TemperatureRho FactorDNA-Directed RNA PolymerasesEscherichia coli ProteinsRho FactorRho protein, E colirpoB protein, E colidiminishing returnsepistasisgene coexpression modulesgene expressionrho termination

Identifiers

PMID39235107
PMCPMC11414761

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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.