The biological functions of FtsH in plant organelle protein homeostasis.

IF 5.7 2区 生物学 Q1 PLANT SCIENCES
Fei Wang, Yafei Qi, Fei Yu
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引用次数: 0

Abstract

Both mitochondria and chloroplasts are capable of driving the electron transport chain reactions for ATP production that are essential for plant growth, development, and stress resilience. The maintenance of organelle protein homeostasis relies on the coordinated assembly of membrane protein complexes and the degradation of unassembled or damaged subunits. FtsH proteins, containing an ATPase domain and a protease domain, are a highly conserved ATP-dependent protease family in photosynthetic organisms. In plants, different FtsH family members are targeted to specific organelle membranes to orchestrate protein homeostasis. This review provides an updated overview of the functions of plant FtsHs in mitochondrial and chloroplastic protein homeostasis, focusing on their protease activity, chaperone-like functions, and substrate processing capabilities. Additionally, it highlights the regulatory mechanisms currently known to modulate the activity and stability of FtsH. Furthermore, we summarize the genetic modifier loci of AtFtsH2/VAR2 encoding the AtFtsH2 subunit of the thylakoid FtsH complex in Arabidopsis and also propose a potential role for the thylakoid FtsH in the degradation of unassembled photosynthetic proteins, particularly under conditions in which the chlorophyll biosynthetic pathway is disrupted.

FtsH在植物细胞器蛋白稳态中的生物学功能。
线粒体和叶绿体都能够驱动电子传递链反应,产生ATP,这对植物的生长、发育和抗逆性至关重要。细胞器蛋白稳态的维持依赖于膜蛋白复合物的协调组装和未组装或受损亚基的降解。FtsH包含一个atp酶结构域和一个蛋白酶结构域,是光合生物中高度保守的atp依赖性蛋白酶家族。在植物中,不同的FtsH家族成员靶向特定的细胞器膜来协调蛋白质稳态。本文综述了植物FtsH在线粒体和叶绿体蛋白稳态中的功能,重点介绍了其蛋白酶活性、伴侣样功能和底物处理能力。此外,它还强调了目前已知的调节FtsH活性和稳定性的调节机制。此外,我们总结了拟南芥中编码类囊体FtsH复合物AtFtsH2亚基的AtFtsH2/VAR2的遗传修饰位点,并提出了类囊体FtsH在降解未组装的光合作用蛋白中的潜在作用,特别是在叶绿素生物合成途径被破坏的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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