School of Life Sciences, Centre for Cell & Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
School of Life Sciences, East China Normal University, Shanghai 200062, China.
Plant Cell. 2023 Nov 30;35(12):4217-4237. doi: 10.1093/plcell/koad227.
Membrane protein homeostasis is fine-tuned by the cellular pathways for vacuolar degradation and recycling, which ultimately facilitate plant growth and cell-environment interactions. The endosomal sorting complex required for transport (ESCRT) machinery plays important roles in regulating intraluminal vesicle (ILV) formation and membrane protein sorting to vacuoles. We previously showed that the plant-specific ESCRT component FYVE DOMAIN PROTEIN REQUIRED FOR ENDOSOMAL SORTING1 (FREE1) performs multiple functions in plants, although the underlying mechanisms remain elusive. In this study, we performed a suppressor screen of the FREE1-RNAi mutant and identified and characterized 2 suppressor of free1 (sof) mutants in Arabidopsis (Arabidopsis thaliana). These mutants, sof10 and sof641, result in a premature stop codon or a missense mutation in AT5G10370, respectively. This gene was named DEAH and RING domain-containing protein as FREE1 suppressor 1 (DRIF1). DRIF1 has a homologous gene, DRIF2, in the Arabidopsis genome with 95% identity to DRIF1. The embryos of drif1 drif2 mutants arrested at the globular stage and formed enlarged multivesicular bodies (MVBs) with an increased number of ILVs. DRIF1 is a membrane-associated protein that coordinates with retromer component sorting nexin 1 to regulate PIN-FORMED2 recycling to the plasma membrane. Altogether, our data demonstrate that DRIF1 is a unique retromer interactor that orchestrates FREE1-mediated ILV formation of MVBs and vacuolar sorting of membrane proteins for degradation in plants.
膜蛋白稳态是通过液泡降解和回收的细胞途径精细调节的,这最终促进了植物的生长和细胞与环境的相互作用。内体分选复合物所需的运输(ESCRT)机制在调节腔内囊泡(ILV)形成和膜蛋白分选到液泡中发挥重要作用。我们之前表明,植物特异性 ESCRT 成分 FYVE 结构域蛋白需要进行内体分选 1(FREE1)在植物中具有多种功能,尽管其潜在机制仍不清楚。在这项研究中,我们对 FREE1-RNAi 突变体进行了抑制子筛选,并在拟南芥中鉴定和表征了 2 个 FREE1 的抑制子突变体(sof)。这些突变体 sof10 和 sof641 分别导致 AT5G10370 中的提前终止密码子或错义突变。该基因被命名为 DEAH 和 RING 结构域蛋白作为 FREE1 抑制子 1(DRIF1)。DRIF1 在拟南芥基因组中有一个同源基因 DRIF2,与 DRIF1 具有 95%的同一性。driF1 driF2 突变体的胚胎在球形阶段停滞,并形成具有增加数量的 ILVs 的增大的多泡体(MVBs)。DRIF1 是一种膜相关蛋白,与逆行成分分选连接蛋白 1 协调,以调节 PIN 形成蛋白 2 向质膜的再循环。总之,我们的数据表明,DRIF1 是一种独特的逆行相互作用因子,协调 FREE1 介导的 MVBs 的 ILV 形成和质膜的膜蛋白降解的液泡分选。