Evidence map›Paper›PMID 41315903›Full record

ArticleBMC plant biology2025

Genome-wide identification of the peanut PITP gene family and functional verification of AhSFH8 in resistance to Aspergillus flavus infection.

Mengjie Cui, Linjie Chen, Zheng Wu, Lei Shi, Xiangru Xu, Meng Zhang, Feiyan Qi, Xiaobo Wang, Jing Xu, Hua Liu and 4 more

Abstract read
In one paragraph

Article in BMC plant biology, 2025. 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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3 · Its place in the literature

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4 · The record

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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

14 authors.

Mengjie CuiInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Linjie ChenInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Zheng WuInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Lei ShiInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Xiangru XuInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Meng ZhangInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Feiyan QiInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Xiaobo WangInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Jing XuInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Hua LiuInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Bingyan HuangInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Wenzhao DongInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China.
Suoyi HanInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China. suoyi_han@126.com.
Xinyou ZhangInstitute of Crop Molecular Breeding, Henan Academy of Agricultural Sciences/The Shennong Laboratory/Key Laboratory of Oil Crops in Huang-Huai-Hai Plains, Ministry of Agriculture and Rural Affairs/Henan Provincial Key Laboratory for Oil Crop Improvement, Zhengzhou, 450002, China. haasxinyou@163.com.

Funding

National Key R&D Program of China 2022YFD1200400the Excellent Youth Fund Project of Henan Academy of Agricultural Sciences 2024YQ03Youth Fund Project of National Natural Science Foundation of China 32301851
6 · The paper itself

Abstract

Phosphatidylinositol transfer proteins (PITPs) are essential in eukaryotes for transporting phosphatidylinositol and phosphatidylcholine monomers across intracellular membranes, and they play key roles in regulating plant growth, signal transduction, stress responses, and other vital biological processes. Arachis hypogaea L., the crop most susceptible to Aspergillus flavus, has not been reported its PITP genes in responses to A. flavus infection. In this study, we performed a genome-wide identification of the PITP gene family in the peanut cultivar Tifrunner using the latest reference genome, and analyzed their expression patterns in different peanut tissues and at various time points after A. flavus inoculation. Furthermore, we cloned a candidate gene, AhSFH8 (a member of the PITP family's SFH subfamily, which contains Sec14-Nodulin or NIJ16 domains) from the highly A. flavus-resistant peanut material "J11" and validated its function via overexpression in tobacco. A total of 85 peanut PITP genes (AhPITPs) were identified, which were classified into three subfamilies and distributed across 20 chromosomes. Segmental duplication was found to be the main driver for the expansion of this family, and gene structure, motif, and conserved domain analyses confirmed their structural conservation. Promoter cis-acting element analysis showed that SFH subfamily members harbored more stress-related elements, suggesting their involvement in stress responses. Expression profiling revealed that three SFH genes (AhSFH8, AhSFH9, AhSFH10) were potentially associated with A. flavus resistance. Cloning of AhSFH8 from "J11" showed its target fragment is 1917 bp in length, with premature translation termination at 1836 bp. Transgenic tobacco overexpressing AhSFH8 exhibited significantly less leaf yellowing and fewer surface spores than wild-type tobacco after A. flavus infection, preliminarily confirming that AhSFH8 enhances A. flavus resistance. Based on gene family identification, promoter analysis, expression patterns and transgenic functional validation, we identified three SFH genes potentially associated with resistance to A. flavus infection. Our findings provide a foundation for understanding the functions of the peanut PITP gene family and the mechanism underlying AhSFH8-mediated resistance to A. flavus infection, while also offering valuable candidate genes for peanut resistance breeding.

Indexed as

ArachisAspergillus flavusDisease ResistancePhospholipid Transfer ProteinsPlant DiseasesPlant ProteinsGene Expression Regulation, PlantGenes, PlantMultigene FamilyPhylogenyPhospholipid Transfer ProteinsPlant ProteinsAhSFH8Aspergillus flavus infectionPeanutPhosphatidylinositol transfer protein (PITP)

Identifiers

PMID41315903
PMCPMC12664188

What Socratic holds

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LicenceCC BY
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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 Socratic graph.