Identification of the interacting proteins of Bambusa pervariabilis × Dendrocalamopsis grandis in response to the transcription factor ApCtf1β in Arthrinium phaeospermum

Arthrinium phaeospermum is the main pathogen that causes Bambusa pervariabilis × Dendrocalamopsis grandis blight. It secretes the cutinase transcription factor ApCtf1β , which has been shown to play an important role in B. pervariabilis × D. grandis virulence. However, knowledge about the interactio...

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Veröffentlicht in:Frontiers in plant science 2022-09, Vol.13, p.991077-991077
Hauptverfasser: Yan, Peng, Yu, Jiawen, Fang, Xinmei, Li, Shuying, Han, Shan, Lin, Tiantian, Liu, Yinggao, Yang, Chunlin, He, Fang, Zhu, Tianhui, Li, Shujiang
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Sprache:eng
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Zusammenfassung:Arthrinium phaeospermum is the main pathogen that causes Bambusa pervariabilis × Dendrocalamopsis grandis blight. It secretes the cutinase transcription factor ApCtf1β , which has been shown to play an important role in B. pervariabilis × D. grandis virulence. However, knowledge about the interaction target genes of ApCtf1β in B. pervariabilis × D. grandis remains limited. A cDNA library for the yeast two-hybrid system was constructed from B. pervariabilis × D. grandis shoots after 168 h treatment with A. phaeospermum . The library was identified as 1.20 × 10 7  cfu, with an average insert >1,000 bp in size and a 100% positive rate, providing a database for the subsequent molecular study of the interaction between A. phaeospermum and B. pervariabilis × D. grandis . The yeast two-hybrid (Y2H), bimolecular fluorescence complementation (BiFC), and glutathione-S-transferase (GST) pull-down assays were used to screen for and identify two ApCtf1β interacting target proteins, BDUbc and BDSKL1 , providing a reliable theoretical basis to study the molecular mechanism underlying B. pervariabilis × D. grandis resistance in response to A. phaeospermum , which would, in turn, establish a platform to develop new strategies for the sustainable and effective control of the blight diseases of forest trees.
ISSN:1664-462X
1664-462X
DOI:10.3389/fpls.2022.991077