2021
DOI: 10.3390/jof7060411
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Transcription Activator Swi6 Interacts with Mbp1 in MluI Cell Cycle Box-Binding Complex and Regulates Hyphal Differentiation and Virulence in Beauveria bassiana

Abstract: Mbp1 protein acts as a DNA-binding protein in MluI cell cycle box-binding complex (MBF) and plays an essential role in filamentous myco-pathogen Beauveria bassiana.In the current study, BbSwi6 (a homologue of yeast Swi6) was functionally characterized in B.bassiana. Both BbSwi6 and BbMbp1 localize in the nucleus and display a direct interaction relationship which is indicated by a yeast two-hybrid assay. BbSwi6 significantly contributes to hyphal growth, asexual sporulation and virulence. On the aerial surface… Show more

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Cited by 20 publications
(16 citation statements)
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“…Autophagosome ultrastructures were examined with TEM ( 24 ), while autophagic flux was measured with the fluorescent reporter method ( 15 ). Specifically, the coding sequences of BbAtg8 and BbAtg8 T were amplified and then cloned into vectors to confer chlorsulfuron resistance ( 50 ). The hybrid gene was transformed into the Δ Bbatg8 strain, and the functioning of BbAtg8 T in selective autophagy was determined by analyzing pexophagy and mitophagy, as previously described ( 15 ).…”
Section: Methodsmentioning
confidence: 99%
“…Autophagosome ultrastructures were examined with TEM ( 24 ), while autophagic flux was measured with the fluorescent reporter method ( 15 ). Specifically, the coding sequences of BbAtg8 and BbAtg8 T were amplified and then cloned into vectors to confer chlorsulfuron resistance ( 50 ). The hybrid gene was transformed into the Δ Bbatg8 strain, and the functioning of BbAtg8 T in selective autophagy was determined by analyzing pexophagy and mitophagy, as previously described ( 15 ).…”
Section: Methodsmentioning
confidence: 99%
“…The obtained fragments were cloned into pTMTB, generating the plasmid p0380-TEF-MCS-YC-bar (p0380TM-YC-B). YN was amplified from pUC35S-cYFP/N (Biogle Co.) with primer pair P37/P38 and integrated into plasmid p0380-TEF-sur ( 57 ), generating p0380-TEF-MCS-YN-sur (p0380TM-YN-S). To test the in vivo protein interaction, the primer pairs P39/P40 and P41/P42 were used to amplified BbATG1 and BbATG3 , respectively.…”
Section: Methodsmentioning
confidence: 99%
“…The indicated strain was cultured on SDAY plates at 25 °C for 7 days, and the resultant conidia were suspended in a 0.02% Tween-80 solution. All phenotypes were compared among the wild-type, Δ Bbsay1, and complementation mutant strains with three parallel experiments [ 7 , 20 ].…”
Section: Methodsmentioning
confidence: 99%