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拟南芥叶绿素酶 1 通过促进 FtsH 介导的光系统 II 修复中 D1 的降解来保护幼叶免受长期光损伤。

Arabidopsis CHLOROPHYLLASE 1 protects young leaves from long-term photodamage by facilitating FtsH-mediated D1 degradation in photosystem II repair.

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources/Guangdong Provincial Key Laboratory of Postharvest Science of Fruits and Vegetables, South China Agricultural University, Guangzhou 510642, People's Republic of China; College of Life Sciences, South China Agricultural University, Guangzhou 510642, People's Republic of China.

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources/Guangdong Provincial Key Laboratory of Postharvest Science of Fruits and Vegetables, South China Agricultural University, Guangzhou 510642, People's Republic of China; College of Horticulture, South China Agricultural University, Guangzhou 510642, People's Republic of China.

出版信息

Mol Plant. 2021 Jul 5;14(7):1149-1167. doi: 10.1016/j.molp.2021.04.006. Epub 2021 Apr 20.

Abstract

The proteolytic degradation of the photodamaged D1 core subunit during the photosystem II (PSII) repair cycle is well understood, but chlorophyll turnover during D1 degradation remains unclear. Here, we report that Arabidopsis thaliana CHLOROPHYLLASE 1 (CLH1) plays important roles in the PSII repair process. The abundance of CLH1 and CLH2 peaks in young leaves and is induced by high-light exposure. Seedlings of clh1 single and clh1-1/2-2 double mutants display increased photoinhibition after long-term high-light exposure, whereas seedlings overexpressing CLH1 have enhanced light tolerance compared with the wild type. CLH1 is localized in the developing chloroplasts of young leaves and associates with the PSII-dismantling complexes RCC1 and RC47, with a preference for the latter upon exposure to high light. Furthermore, degradation of damaged D1 protein is retarded in young clh1-1/2-2 leaves after 18-h high-light exposure but is rescued by the addition of recombinant CLH1 in vitro. Moreover, overexpression of CLH1 in a variegated mutant (var2-2) that lacks thylakoid protease FtsH2, with which CLH1 interacts, suppresses the variegation and restores D1 degradation. A var2-2 clh1-1/2-2 triple mutant shows more severe variegation and seedling death. Taken together, these results establish CLH1 as a long-sought chlorophyll dephytylation enzyme that is involved in PSII repair and functions in long-term adaptation of young leaves to high-light exposure by facilitating FtsH-mediated D1 degradation.

摘要

在光系统 II (PSII) 修复循环中,光损伤的 D1 核心亚基的蛋白水解降解过程已经得到很好的理解,但 D1 降解过程中的叶绿素周转仍不清楚。在这里,我们报告说拟南芥叶绿素酶 1 (CLH1) 在 PSII 修复过程中发挥重要作用。CLH1 和 CLH2 的丰度在幼叶中达到峰值,并受高光暴露诱导。clh1 单突变体和 clh1-1/2-2 双突变体的幼苗在长期高光暴露后表现出增加的光抑制,而过表达 CLH1 的幼苗与野生型相比具有增强的耐光性。CLH1 定位于幼叶发育中的叶绿体,并与 PSII 解体复合物 RCC1 和 RC47 相关联,在暴露于高光下时,后者优先结合。此外,在 18 小时高光暴露后,年轻 clh1-1/2-2 叶片中受损 D1 蛋白的降解被延迟,但在体外添加重组 CLH1 后得到挽救。此外,CLH1 在缺乏与 CLH1 相互作用的类囊体蛋白酶 FtsH2 的斑驳突变体 (var2-2) 中的过表达,抑制了斑驳,并恢复了 D1 的降解。var2-2 clh1-1/2-2 三重突变体表现出更严重的斑驳和幼苗死亡。总之,这些结果确立了 CLH1 作为一种长期以来被寻找的叶绿素脱植基酶,它参与 PSII 修复,并通过促进 FtsH 介导的 D1 降解,在幼叶对高光暴露的长期适应中发挥作用。

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