The Fungal Transcription Factor BcTbs1 from Botrytis cinerea Promotes Pathogenicity via Host Cellulose Degradation.
Yinshan ZhangChengguo JiaYue LiuGuihua LiBin LiWuliang ShiYubin ZhangJie HouQing-Ming QinMingzhe ZhangJian-Chun QinPublished in: Journal of agricultural and food chemistry (2024)
Zn(II)2Cys6 proteins constitute the largest group of fungal-specific transcription factors. However, little is known about their functions in the crop killer Botrytis cinerea . In this work, a T-DNA insertion strain M13448 was identified which was inserted into the Zn(II)2Cys6 TF-encoding gene BcTBS1 . Knockout of BcTBS1 did not affect mycelia growth, appressorium formation, and sclerotium germination, but impaired fungal conidiation, conidial morphogenesis, conidial germination, infection cushion development, and sclerotial formation. Accordingly, Δ Bctbs1 mutants showed reduced virulence in its host plants. Further study proved that BcTBS1 , BCIN_15g03870 , and BCIN_12g06630 were induced by cellulose. Subsequent cellulase activity assays revealed that the loss of BcTBS1 significantly decreased cellulase activity. In addition, we verified that the BCIN_15g03870 and BCIN_12g06630 genes were positive regulated by BcTBS1 by quantitative real-time reverse-transcription-polymerase chain reaction (qRT-PCR). Taken together, these results suggested that BcTBS1 can promote pathogenicity by modulating cellulase-encoding genes that participate in host cellulose degradation.
Keyphrases
- transcription factor
- genome wide identification
- ionic liquid
- genome wide
- biofilm formation
- dna binding
- escherichia coli
- heavy metals
- pseudomonas aeruginosa
- staphylococcus aureus
- aqueous solution
- silver nanoparticles
- climate change
- cell wall
- copy number
- high throughput
- high resolution
- single molecule
- bioinformatics analysis
- gene expression
- circulating tumor
- single cell
- cell free