Unveiling genetic anchors in saccharomyces cerevisiae: QTL mapping identifies IRA2 as a key player in ethanol tolerance and beyond.


Journal

Molecular genetics and genomics : MGG
ISSN: 1617-4623
Titre abrégé: Mol Genet Genomics
Pays: Germany
ID NLM: 101093320

Informations de publication

Date de publication:
26 Oct 2024
Historique:
received: 08 05 2024
accepted: 12 10 2024
medline: 27 10 2024
pubmed: 27 10 2024
entrez: 27 10 2024
Statut: epublish

Résumé

Ethanol stress in Saccharomyces cerevisiae is a well-studied phenomenon, but pinpointing specific genes or polymorphisms governing ethanol tolerance remains a subject of ongoing debate. Naturally found in sugar-rich environments, this yeast has evolved to withstand high ethanol concentrations, primarily produced during fermentation in the presence of suitable oxygen or sugar levels. Originally a defense mechanism against competing microorganisms, yeast-produced ethanol is now a cornerstone of brewing and bioethanol industries, where customized yeasts require high ethanol resistance for economic viability. However, yeast strains exhibit varying degrees of ethanol tolerance, ranging from 8 to 20%, making the genetic architecture of this trait complex and challenging to decipher. In this study, we introduce a novel QTL mapping pipeline to investigate the genetic markers underlying ethanol tolerance in an industrial bioethanol S. cerevisiae strain. By calculating missense mutation frequency in an allele located in a prominent QTL region within a population of 1011 S. cerevisiae strains, we uncovered rare occurrences in gene IRA2. Following molecular validation, we confirmed the significant contribution of this gene to ethanol tolerance, particularly in concentrations exceeding 12% of ethanol. IRA2 pivotal role in stress tolerance due to its participation in the Ras-cAMP pathway was further supported by its involvement in other tolerance responses, including thermotolerance, low pH tolerance, and resistance to acetic acid. Understanding the genetic basis of ethanol stress in S. cerevisiae holds promise for developing robust yeast strains tailored for industrial applications.

Identifiants

pubmed: 39461918
doi: 10.1007/s00438-024-02196-5
pii: 10.1007/s00438-024-02196-5
doi:

Substances chimiques

Ethanol 3K9958V90M
Saccharomyces cerevisiae Proteins 0
IRA2 protein, S cerevisiae 0
GTPase-Activating Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103

Subventions

Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : 2022/07061-4
Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : 2022/13111-4
Organisme : Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
ID : 88887.479699/2020-0

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Larissa Escalfi Tristão (LE)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Lara Isensee Saboya de Sousa (LIS)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Beatriz de Oliveira Vargas (B)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Juliana José (J)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Marcelo Falsarella Carazzolle (MF)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Eduardo Menoti Silva (EM)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Juliana Pimentel Galhardo (JP)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

Gonçalo Amarante Guimarães Pereira (GAG)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil. goncalo@unicamp.br.

Fellipe da Silveira Bezerra de Mello (FDSB)

Departamento de Genética, Evolução, Microbiologia e Imunologia, Unicamp, Campinas, SP, Brazil.

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