Photoexcited CRY1 physically interacts with ATG8 to regulate selective autophagy of HY5 and photomorphogenesis in Arabidopsis.

Lu Jiang,Shilong Zhang,Yuting Niu,Guangqiong Yang,Jiachen Zhao,Huishan Liu,Minyu Xiong,Lingyi Xie,Zhilei Mao,Tongtong Guo,Hong-Quan Yang,Wenxiu Wang
{"title":"Photoexcited CRY1 physically interacts with ATG8 to regulate selective autophagy of HY5 and photomorphogenesis in Arabidopsis.","authors":"Lu Jiang,Shilong Zhang,Yuting Niu,Guangqiong Yang,Jiachen Zhao,Huishan Liu,Minyu Xiong,Lingyi Xie,Zhilei Mao,Tongtong Guo,Hong-Quan Yang,Wenxiu Wang","doi":"10.1093/plcell/koaf196","DOIUrl":null,"url":null,"abstract":"Cryptochromes (CRYs) are blue light photoreceptors that regulate various light responses in plants, including photomorphogenesis. Autophagy is a tightly controlled intracellular degradation pathway that plays a critical role in plant growth and development. CRY signaling inhibits the 26S proteasome-dependent degradation of LONG HYPOCOTYL 5 (HY5) through interactions with the CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1)-SUPPRESSOR OF PHYA-105 1 (SPA1) complex. However, whether CRY1 mediates the blue light-driven regulation of photomorphogenesis by regulating the autophagic degradation of HY5 remains unclear. Here, we show that CRY1 directly interacts with ATG8, a key player in selective autophagy, in a blue light-dependent manner in Arabidopsis (Arabidopsis thaliana). ATG8 and ATG5/ATG7 act genetically downstream of CRY1, but upstream of HY5, to regulate photomorphogenesis. In darkness, AUTOPHAGY-RELATED8 (ATG8) physically interacts with HY5 to facilitate its autophagic degradation and promote skotomorphogenesis. Under blue light, the CRY1-ATG8 interaction inhibits the ATG8-HY5 interaction, suppressing the nuclear export and co-localization of ATG8 and HY5 to the autophagosome, and HY5 degradation in the vacuole. This study reveals how CRY1-mediated blue light signaling regulates HY5 autophagy, which enables plants to fine-tune photomorphogenic development in response to light and nutrient availability.","PeriodicalId":501012,"journal":{"name":"The Plant Cell","volume":"193 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Cell","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/plcell/koaf196","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

Cryptochromes (CRYs) are blue light photoreceptors that regulate various light responses in plants, including photomorphogenesis. Autophagy is a tightly controlled intracellular degradation pathway that plays a critical role in plant growth and development. CRY signaling inhibits the 26S proteasome-dependent degradation of LONG HYPOCOTYL 5 (HY5) through interactions with the CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1)-SUPPRESSOR OF PHYA-105 1 (SPA1) complex. However, whether CRY1 mediates the blue light-driven regulation of photomorphogenesis by regulating the autophagic degradation of HY5 remains unclear. Here, we show that CRY1 directly interacts with ATG8, a key player in selective autophagy, in a blue light-dependent manner in Arabidopsis (Arabidopsis thaliana). ATG8 and ATG5/ATG7 act genetically downstream of CRY1, but upstream of HY5, to regulate photomorphogenesis. In darkness, AUTOPHAGY-RELATED8 (ATG8) physically interacts with HY5 to facilitate its autophagic degradation and promote skotomorphogenesis. Under blue light, the CRY1-ATG8 interaction inhibits the ATG8-HY5 interaction, suppressing the nuclear export and co-localization of ATG8 and HY5 to the autophagosome, and HY5 degradation in the vacuole. This study reveals how CRY1-mediated blue light signaling regulates HY5 autophagy, which enables plants to fine-tune photomorphogenic development in response to light and nutrient availability.
光激发CRY1与ATG8物理相互作用调节拟南芥中HY5的选择性自噬和光形态发生。
隐色素是一种蓝光感受器,调节植物的各种光反应,包括光形态发生。自噬是一种受到严格控制的细胞内降解途径,在植物生长发育中起着至关重要的作用。CRY信号通过与phya - 1051 (SPA1)复合体的组成型光形态形成1 (COP1)-抑制因子相互作用,抑制26S蛋白酶体依赖的长下胚轴5 (HY5)降解。然而,CRY1是否通过调节HY5的自噬降解介导蓝光驱动的光形态发生调控尚不清楚。在这里,我们发现CRY1直接与拟南芥(拟南芥)中选择性自噬的关键角色ATG8以蓝光依赖的方式相互作用。ATG8和ATG5/ATG7基因作用于CRY1的下游,但在HY5的上游,调节光形态发生。在黑暗中,AUTOPHAGY-RELATED8 (ATG8)与HY5发生物理相互作用,促进其自噬降解,促进大脑形态形成。在蓝光下,CRY1-ATG8相互作用抑制ATG8-HY5相互作用,抑制ATG8和HY5向自噬体的核输出和共定位,抑制HY5在液泡中的降解。该研究揭示了cry1介导的蓝光信号如何调节HY5自噬,使植物能够根据光和养分的可用性微调光形态形成的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信