The transcription factors ERF105 and NAC72 regulate expression of a sugar transporter gene and hexose accumulation in grape.

IF 10 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Plant Cell Pub Date : 2024-12-18 DOI:10.1093/plcell/koae326
Lizhen Lu, Serge Delrot, Peige Fan, Zhan Zhang, Die Wu, Fengqin Dong, Pedro García-Caparros, Shaohua Li, Zhanwu Dai, Zhenchang Liang
{"title":"The transcription factors ERF105 and NAC72 regulate expression of a sugar transporter gene and hexose accumulation in grape.","authors":"Lizhen Lu, Serge Delrot, Peige Fan, Zhan Zhang, Die Wu, Fengqin Dong, Pedro García-Caparros, Shaohua Li, Zhanwu Dai, Zhenchang Liang","doi":"10.1093/plcell/koae326","DOIUrl":null,"url":null,"abstract":"<p><p>Sugar transport plays a pivotal role in determining the productivity of plants and their capacity to act as carbon sinks. In the major fruit crop grapevine (Vitis vinifera L.), the transporter gene Vitis vinifera Sugars Will Eventually be Exported Transporter 15 (VvSWEET15)is strongly expressed during berry ripening. However, the specific functions of VvSWEET15 and the mechanisms governing its transcriptional regulation remain largely unresolved. Here, we demonstrate that VvSWEET15 functions as a hexose transporter whose expression is associated with the strong sugar accumulation that starts at the véraison stage. We also characterize VvERF105 as a repressor that binds to the LTR-binding element in the VvSWEET15 promoter, thereby down-regulating its expression and inhibiting hexose accumulation at the pre-véraison stage. In contrast, VvNAC72 is an activator that binds to the VvNAC72-binding domain (CACATG) and promotes VvSWEET15 expression and hexose accumulation at post-véraison stages. Both transcription factors and VvSWEET15 are preferentially expressed in phloem cells. These results demonstrate that the balance between transcriptional activators and repressors is critical in regulating VvSWEET15 expression in sink organs. Further understanding of these processes will help improve plant productivity and their potential to be used as carbon sinks.</p>","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plcell/koae326","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Sugar transport plays a pivotal role in determining the productivity of plants and their capacity to act as carbon sinks. In the major fruit crop grapevine (Vitis vinifera L.), the transporter gene Vitis vinifera Sugars Will Eventually be Exported Transporter 15 (VvSWEET15)is strongly expressed during berry ripening. However, the specific functions of VvSWEET15 and the mechanisms governing its transcriptional regulation remain largely unresolved. Here, we demonstrate that VvSWEET15 functions as a hexose transporter whose expression is associated with the strong sugar accumulation that starts at the véraison stage. We also characterize VvERF105 as a repressor that binds to the LTR-binding element in the VvSWEET15 promoter, thereby down-regulating its expression and inhibiting hexose accumulation at the pre-véraison stage. In contrast, VvNAC72 is an activator that binds to the VvNAC72-binding domain (CACATG) and promotes VvSWEET15 expression and hexose accumulation at post-véraison stages. Both transcription factors and VvSWEET15 are preferentially expressed in phloem cells. These results demonstrate that the balance between transcriptional activators and repressors is critical in regulating VvSWEET15 expression in sink organs. Further understanding of these processes will help improve plant productivity and their potential to be used as carbon sinks.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Plant Cell
Plant Cell 生物-生化与分子生物学
CiteScore
16.90
自引率
5.20%
发文量
337
审稿时长
2.4 months
期刊介绍: Title: Plant Cell Publisher: Published monthly by the American Society of Plant Biologists (ASPB) Produced by Sheridan Journal Services, Waterbury, VT History and Impact: Established in 1989 Within three years of publication, ranked first in impact among journals in plant sciences Maintains high standard of excellence Scope: Publishes novel research of special significance in plant biology Focus areas include cellular biology, molecular biology, biochemistry, genetics, development, and evolution Primary criteria: articles provide new insight of broad interest to plant biologists and are suitable for a wide audience Tenets: Publish the most exciting, cutting-edge research in plant cellular and molecular biology Provide rapid turnaround time for reviewing and publishing research papers Ensure highest quality reproduction of data Feature interactive format for commentaries, opinion pieces, and exchange of information in review articles, meeting reports, and insightful overviews.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信