Xiaoru Kang, Shuai Huang, Yuming Feng, Rumeng Fu, Fengjuan Tang, Long Zheng, Peijun Li, Nan Chao, Li Liu
{"title":"SWEET transporters and their potential roles in response to abiotic and biotic stresses in mulberry","authors":"Xiaoru Kang, Shuai Huang, Yuming Feng, Rumeng Fu, Fengjuan Tang, Long Zheng, Peijun Li, Nan Chao, Li Liu","doi":"10.48130/bpr-2023-0006","DOIUrl":null,"url":null,"abstract":"Mulberry ( Morus spp ., Moraceae) is a traditional economic crop plant and is also being gradually utilized as a beverage plant. SWEETs (Sugars Will Eventually be Exported Transporter) are important sugar transporters involved in various biological processes and responses to various stresses. However, SWEETs in mulberry are still poorly studied without a comprehensive functional analysis of SWEETs . In the present study, a total of 24 SWEETs were identified using the Morus alba (Ma) genome. Phylogenetic analysis showed that these 24 MaSWEETs were clustered with SWEETs from Arabidopsis , Populus and Oryza and fell into four clades. MaSWEET s in the same clade are likely to pose similar intron/exon patterns. These MaSWEET s distributed on 12 chromosomes and tandem duplication and block duplication were responsible for the expansion of SWEETs in mulberry. Transmembrane domains and conserved active sites of Tyr and Asp were observed in MaSWEETs. Cis-elements in promoter regions of MaSWEET s indicated the possible function of MaSWEET s in response to hormones and environment stimulus. MaSWEET s showed quite different expression preference in tissues and organs indicating the possible function divergence. In addition, most MaSWEETs showed a disturbed expression levels in response to various abiotic stresses and Ciboria shiraiana infection. MaSWEET1a was functionally characterized as a negative regulator of resistance to C. shiraiana infection based on in vivo transient overexpression of MaSWEET1a in tobacco and down-regulation of MaSWEET1a/b in mulberry. Our results provided foundation for further functional dissection of SWEETs in mulberry and a potential regulator for genetic modification.","PeriodicalId":223765,"journal":{"name":"Beverage Plant Research","volume":"25 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Beverage Plant Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.48130/bpr-2023-0006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Mulberry ( Morus spp ., Moraceae) is a traditional economic crop plant and is also being gradually utilized as a beverage plant. SWEETs (Sugars Will Eventually be Exported Transporter) are important sugar transporters involved in various biological processes and responses to various stresses. However, SWEETs in mulberry are still poorly studied without a comprehensive functional analysis of SWEETs . In the present study, a total of 24 SWEETs were identified using the Morus alba (Ma) genome. Phylogenetic analysis showed that these 24 MaSWEETs were clustered with SWEETs from Arabidopsis , Populus and Oryza and fell into four clades. MaSWEET s in the same clade are likely to pose similar intron/exon patterns. These MaSWEET s distributed on 12 chromosomes and tandem duplication and block duplication were responsible for the expansion of SWEETs in mulberry. Transmembrane domains and conserved active sites of Tyr and Asp were observed in MaSWEETs. Cis-elements in promoter regions of MaSWEET s indicated the possible function of MaSWEET s in response to hormones and environment stimulus. MaSWEET s showed quite different expression preference in tissues and organs indicating the possible function divergence. In addition, most MaSWEETs showed a disturbed expression levels in response to various abiotic stresses and Ciboria shiraiana infection. MaSWEET1a was functionally characterized as a negative regulator of resistance to C. shiraiana infection based on in vivo transient overexpression of MaSWEET1a in tobacco and down-regulation of MaSWEET1a/b in mulberry. Our results provided foundation for further functional dissection of SWEETs in mulberry and a potential regulator for genetic modification.