Evidence map›Paper›PMID 41947219›Full record

ArticleMolecular horticulture2026

Dissecting G-protein signaling pathways in the fruit pathogen Penicillium expansum: implications for pathogenesis and patulin production.

Yong Chen, Dongying Xu, Mengyang Xing, Tong Chen, Boqiang Li, Shiping Tian

Abstract read
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Article in Molecular horticulture, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yong Chen *State Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Dongying Xu *State Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Mengyang XingState Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Tong ChenState Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Boqiang LiState Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China. bqli@ibcas.ac.cn.
Shiping TianState Key Laboratory of Plant Diversity and Specialty Crops, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China. tshiping@163.com.ORCID http://orcid.org/0000-0002-5883-0037

Funding

National Key R&D Program of China 2021YFD2100501National Key R&D Program of China 2021YFD2100505National Natural Science Foundation of China 32261133624National Natural Science Foundation of China 32372405National Natural Science Foundation of China 32430082
6 · The paper itself

Abstract

Penicillium expansum causes blue mold in various fruits and produces patulin, a mycotoxin of significant economic and food safety concern. Fungal infection relies on sensing and adapting to environmental cues via G-protein signaling pathways. Despite its importance, the understanding of how these pathways contribute to the infection process and patulin biosynthesis of P. expansum remains limited. Here, we characterized five G protein subunits (PeGαⅠ, PeGαⅡ, PeGαⅢ, PeGβ, and PeGγ), all highly expressed during hyphal growth and fruit infection. Deletion of these G protein genes leads to various defects in hyphal growth, virulence, and patulin production. Notably, ΔPeGαⅠ, ΔPeGβ, and ΔPeGγ mutants showed severe defects, with minimal disease symptoms in early infection stages and at least a 50% decrease in patulin production. These mutants displayed straight hyphal growth, reduced branching, and significantly decreased vitality. RNA sequencing analysis revealed that this abnormal growth is governed by pathways associated with fungal hyphal polarity. Furthermore, PeGαⅠ and PeGαⅢ are crucial for cAMP-PKA signaling, while PeGβ and PeGγ modulate MAPK signaling, both pathways influencing virulence and patulin production. Together, these findings provide evidence that G proteins regulate virulence and patulin production through the regulation of downstream pathways and their broader effects on fungal hyphal polarity.

Indexed as

Fungal hyphal polarityG-protein signaling pathwaysPathogenicityPatulin productionPenicillium expansum

Identifiers

PMID41947219
PMCPMC13059215

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