# The Benzoylation of the Splicing Factor Skip Is Critical for Development, Oxidative Stress Response and Pathogenicity in Aspergillus flavus

## TL;DR

This paper shows that the Skip protein and its benzoylation are essential for the growth, stress response, and pathogenicity of Aspergillus flavus, a fungus that infects crops.

## Contribution

The study identifies lysine 325 as a benzoylated site on Skip and reveals its role in fungal development and pathogenicity.

## Key findings

- Single-copy deletion of Skip in A. flavus caused slowed growth and reduced spore formation.
- Benzoylation of Skip at lysine 325 is catalyzed by EsaA and is critical for morphogenesis and stress adaptation.
- Mutation of K325 impaired pathogenicity and aflatoxin biosynthesis in A. flavus.

## Abstract

Alternative splicing of pre-mRNA is a crucial mechanism in gene expression regulation. As a core component of the spliceosome, the biological function of the Skip protein in Aspergillus flavus remains unknown. Quantitative real-time PCR (qPCR) analysis revealed the presence of two skip gene copies in A. flavus. Single-copy deletion of Skip resulted in slowed growth, reduced conidiation, abolished sclerotial formation, increased aflatoxin biosynthesis, and diminished crop colonization. Meanwhile, Skip was found to regulate the oxidative stress response by modulating the alternative splicing of yapA. Subsequently, immunoprecipitation and Western blot analyses identified lysine 325 (K325) as the benzoylated site on the Skip protein, which catalyzed by the acyltransferase EsaA. Mutation of benzoylated site K325 directly impaired fungal morphogenesis, pathogenicity, and stress adaptation. These findings established the crucial role of Skip and its benzoylation in A. flavus and suggested a potential target for controlling its infection in important crops.