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Combining Transcriptome Analysis and GWAS for Identification and Validation of Marker Genes in the - Pathosystem

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Journal PeerJ
Date 2021 Apr 8
PMID 33828924
Citations 1
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Abstract

Vascular wilt, caused by the pathogen f. sp. (), is a major disease of cape gooseberry ( L.) in Andean countries. Despite the economic losses caused by this disease, there are few studies related to molecular mechanisms in the - pathosystem as a useful tool for crop improvement. This study evaluates eight candidate genes associated with this pathosystem, using real-time quantitative PCR (RT-qPCR). The genes were identified and selected from 1,653 differentially expressed genes (DEGs) derived from RNA-Seq analysis and from a previous genome-wide association study (GWAS) of this plant-pathogen interaction. Based on the RT-qPCR analysis, the tubuline () reference gene was selected for its highly stable expression in cape gooseberry. The RT-qPCR validation of the candidate genes revealed the biological variation in their expression according to their known biological function. Three genes related to the first line of resistance/defense responses were highly expressed earlier during infection in a susceptible genotype, while three others were overexpressed later, mostly in the tolerant genotype. These genes are mainly involved in signaling pathways after pathogen recognition, mediated by hormones such as ethylene and salicylic acid. This study provided the first insight to uncover the molecular mechanism from the - pathosystem. The genes validated here have important implications in the disease progress and allow a better understanding of the defense response in cape gooseberry at the molecular level. Derived molecular markers from these genes could facilitate the identification of tolerant/susceptible genotypes for use in breeding schemes.

Citing Articles

Advances in molecular research: applications in authentication, genetic diversity, phylogenetics, functional genes, and omics.

Jiang Y, Jin Y, Shan Y, Zhong Q, Wang H, Shen C Front Plant Sci. 2024; 15:1407625.

PMID: 38993935 PMC: 11236614. DOI: 10.3389/fpls.2024.1407625.

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