Ye Hao, Ji Changyang, Guo Rongfang, Jiang Liwen
School of Life Sciences, Centre for Cell and Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong, China.
College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou, China.
Front Plant Sci. 2020 Apr 24;11:477. doi: 10.3389/fpls.2020.00477. eCollection 2020.
Autophagy is an intracellular trafficking and degradation system for recycling of damaged organelles, mis-folded proteins and cytoplasmic constituents. Autophagy can be divided into non-selective autophagy and selective autophagy according to the cargo specification. Key to the process is the timely formation of the autophagosome, a double-membrane structure which is responsible for the delivery of damaged organelles and proteins to lysosomes or vacuoles for their turnover. Autophagosomes are formed by the closure of cup-shaped phagophore which depends on the proper communication with membrane contributors. The endoplasmic reticulum (ER) is a major membrane source for autophagosome biogenesis whereby the ER connects with phagophore through membrane contact sites (MCSs). MCSs are closely apposed domains between organelle membranes where lipids and signals are exchanged. Lipid transfer proteins (LTPs) are a large family of proteins including Oxysterol-binding protein related proteins (ORP) which can be found at MCSs and mediate lipid transfer in mammals and yeast. In addition, interaction between autophagosomes and other organelles can also be detected in selective autophagy for selection and degradation of various damaged organelles. Selective autophagy is mediated by the binding of a receptor or an adaptor between a cargo and an autophagosome. Here we summarize what we know about the MCS between autophagosomes and other organelles in eukaryotes. We then discuss progress in our understanding about ORPs at MCSs in plants and the underlying mechanisms of selective autophagy in plants with a focus on receptors/adaptors that are involved in the interaction of the autophagosome with other cytoplasmic constituents, including the Neighbor of BRCA1 gene 1 (NBR1), ATG8-interacting protein 1 (ATI1), Regulatory Particle Non-ATPase 10 (RPN10), and Dominant Suppressor of KAR2 (DSK2).
自噬是一种细胞内运输和降解系统,用于回收受损细胞器、错误折叠的蛋白质和细胞质成分。根据货物规格,自噬可分为非选择性自噬和选择性自噬。该过程的关键是自噬体的及时形成,自噬体是一种双膜结构,负责将受损细胞器和蛋白质输送到溶酶体或液泡进行周转。自噬体由杯状吞噬泡的封闭形成,这取决于与膜供体的适当通讯。内质网(ER)是自噬体生物发生的主要膜来源,内质网通过膜接触位点(MCSs)与吞噬泡相连。MCSs是细胞器膜之间紧密相邻的区域,脂质和信号在其中交换。脂质转移蛋白(LTPs)是一大类蛋白质,包括氧化固醇结合蛋白相关蛋白(ORP),它们可在MCSs处发现,并介导哺乳动物和酵母中的脂质转移。此外,在选择性自噬中也可检测到自噬体与其他细胞器之间的相互作用,用于选择和降解各种受损细胞器。选择性自噬由货物与自噬体之间的受体或衔接子的结合介导。在这里,我们总结了我们对真核生物中自噬体与其他细胞器之间的MCS的了解。然后,我们讨论了我们对植物中MCSs处的ORPs的理解进展以及植物中选择性自噬的潜在机制,重点关注参与自噬体与其他细胞质成分相互作用的受体/衔接子,包括BRCA1基因1的邻居(NBR1)、与ATG8相互作用的蛋白1(ATI1)、调节颗粒非ATP酶1(RPN10)和KAR2的显性抑制因子(DSK2)。