The ASH1-PEX16 regulatory pathway controls peroxisome biogenesis for appressorium-mediated insect infection by a fungal pathogen.
Lili WangYiling LaiJingjing ChenXuan CaoWeilu ZhengLing DongYitong ZhengFang LiGang WeiSibao WangPublished in: Proceedings of the National Academy of Sciences of the United States of America (2023)
Entomopathogenic fungi infect insects by penetrating through the cuticle into the host body. To breach the host cuticle, some fungal pathogens produce specialized infection cells called appressoria, which develop enormous turgor pressure to allow cuticle penetration. However, regulatory mechanisms underlying appressorium turgor generation are poorly understood. Here, we show that the histone lysine methyltransferase ASH1 in the insecticidal fungus Metarhizium robertsii , which is strongly induced during infection of the mosquito cuticle, regulates appressorium turgor generation and cuticle penetration by activating the peroxin gene Mrpex16 via H3K36 dimethylation. MrPEX16 is required for the biogenesis of peroxisomes that participate in lipid catabolism and further promotes the hydrolysis of triacylglycerols stored in lipid droplets to produce glycerol for turgor generation, facilitating appressorium-mediated insect infection. Together, the ASH1-PEX16 pathway plays a pivotal role in regulating peroxisome biogenesis to promote lipolysis for appressorium turgor generation, providing insights into the molecular mechanisms underlying fungal pathogenesis.
Keyphrases
- transcription factor
- municipal solid waste
- aedes aegypti
- dna methylation
- adipose tissue
- palliative care
- gene expression
- induced apoptosis
- sewage sludge
- risk assessment
- fatty acid
- genome wide
- copy number
- cell wall
- zika virus
- cell death
- candida albicans
- multidrug resistant
- room temperature
- endoplasmic reticulum stress
- cell cycle arrest
- anaerobic digestion
- pi k akt