{"title":"两种MYB转录因子相互作用抑制香蕉细胞壁代谢和淀粉降解基因的表达","authors":"Ting-ting Luo, Hui Zhang, Hai-ke Tan, Li-ting Zhang, Wei Wei, Wei Shan, Jian-fei Kuang, Jian-ye Chen, Wang-jin Lu, Ying-ying Yang","doi":"10.1093/plphys/kiaf239","DOIUrl":null,"url":null,"abstract":"Banana (Musa acuminata, AAA group) fruit softening severely affects postharvest quality, yet the molecular regulatory networks governing this process remain incompletely understood. In this study, we found that the overexpression of MaMYB44 in bananas and tomatoes delayed fruit firmness loss and starch degradation. In addition, MaMYB44 interacted with MaMYB73 (another member of the R2R3-MYB transcription factor family), which also functioned as a repressor of fruit firmness loss and starch degradation. To elucidate the regulatory network of these transcription factors, we performed a genome-wide co-target gene analysis using DNA affinity purification sequencing (DAP-Seq). The results showed that MaMYB44 and MaMYB73 co-targeted the cell wall metabolism gene expansin A15 (MaEXPA15) and the starch degradation gene β-amylase3 (MaBAM3). Notably, the interaction of MaMYB44 and MaMYB73 enhanced their binding affinity and inhibitory effects on MaEXPA15 and MaBAM3. This study uncovers a regulatory mechanism in which MaMYB44 and MaMYB73 form a complex to inhibit the expression of genes involved in fruit firmness loss and starch degradation. These findings provide perspectives on controlling fruit softening and idenitify important targets for improving postharvest quality.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"15 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two MYB transcription factors interact to inhibit the expression of cell wall metabolism and starch degradation genes in banana\",\"authors\":\"Ting-ting Luo, Hui Zhang, Hai-ke Tan, Li-ting Zhang, Wei Wei, Wei Shan, Jian-fei Kuang, Jian-ye Chen, Wang-jin Lu, Ying-ying Yang\",\"doi\":\"10.1093/plphys/kiaf239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Banana (Musa acuminata, AAA group) fruit softening severely affects postharvest quality, yet the molecular regulatory networks governing this process remain incompletely understood. In this study, we found that the overexpression of MaMYB44 in bananas and tomatoes delayed fruit firmness loss and starch degradation. In addition, MaMYB44 interacted with MaMYB73 (another member of the R2R3-MYB transcription factor family), which also functioned as a repressor of fruit firmness loss and starch degradation. To elucidate the regulatory network of these transcription factors, we performed a genome-wide co-target gene analysis using DNA affinity purification sequencing (DAP-Seq). The results showed that MaMYB44 and MaMYB73 co-targeted the cell wall metabolism gene expansin A15 (MaEXPA15) and the starch degradation gene β-amylase3 (MaBAM3). Notably, the interaction of MaMYB44 and MaMYB73 enhanced their binding affinity and inhibitory effects on MaEXPA15 and MaBAM3. This study uncovers a regulatory mechanism in which MaMYB44 and MaMYB73 form a complex to inhibit the expression of genes involved in fruit firmness loss and starch degradation. These findings provide perspectives on controlling fruit softening and idenitify important targets for improving postharvest quality.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/plphys/kiaf239\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf239","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Two MYB transcription factors interact to inhibit the expression of cell wall metabolism and starch degradation genes in banana
Banana (Musa acuminata, AAA group) fruit softening severely affects postharvest quality, yet the molecular regulatory networks governing this process remain incompletely understood. In this study, we found that the overexpression of MaMYB44 in bananas and tomatoes delayed fruit firmness loss and starch degradation. In addition, MaMYB44 interacted with MaMYB73 (another member of the R2R3-MYB transcription factor family), which also functioned as a repressor of fruit firmness loss and starch degradation. To elucidate the regulatory network of these transcription factors, we performed a genome-wide co-target gene analysis using DNA affinity purification sequencing (DAP-Seq). The results showed that MaMYB44 and MaMYB73 co-targeted the cell wall metabolism gene expansin A15 (MaEXPA15) and the starch degradation gene β-amylase3 (MaBAM3). Notably, the interaction of MaMYB44 and MaMYB73 enhanced their binding affinity and inhibitory effects on MaEXPA15 and MaBAM3. This study uncovers a regulatory mechanism in which MaMYB44 and MaMYB73 form a complex to inhibit the expression of genes involved in fruit firmness loss and starch degradation. These findings provide perspectives on controlling fruit softening and idenitify important targets for improving postharvest quality.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.