MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.
J Cell Sci. 2024 Sep 1;137(17). doi: 10.1242/jcs.262160. Epub 2024 Sep 6.
Golgi-resident enzymes remain in place while their substrates flow through from the endoplasmic reticulum to elsewhere in the cell. COPI-coated vesicles bud from the Golgi to recycle Golgi residents to earlier cisternae. Different enzymes are present in different parts of the stack, and one COPI adaptor protein, GOLPH3, acts to recruit enzymes into vesicles in part of the stack. Here, we used proximity biotinylation to identify further components of intra-Golgi vesicles and found FAM114A2, a cytosolic protein. Affinity chromatography with FAM114A2, and its paralogue FAM114A1, showed that they bind to Golgi-resident membrane proteins, with membrane-proximal basic residues in the cytoplasmic tail being sufficient for the interaction. Deletion of both proteins from U2OS cells did not cause substantial defects in Golgi function. However, a Drosophila orthologue of these proteins (CG9590/FAM114A) is also localised to the Golgi and binds directly to COPI. Drosophila mutants lacking FAM114A have defects in glycosylation of glue proteins in the salivary gland. Thus, the FAM114A proteins bind Golgi enzymes and are candidate adaptors to contribute specificity to COPI vesicle recycling in the Golgi stack.
高尔基驻留酶在其底物从内质网流向细胞的其他部位时保持原位。COP1 包被小泡从高尔基体出芽,将高尔基体驻留蛋白重新循环到早期的潴泡。不同的酶存在于堆叠的不同部分,一种 COPI 衔接蛋白 GOLPH3 部分地作用于将酶募集到小泡中。在这里,我们使用邻近生物素化来鉴定高尔基体内小泡的其他成分,并发现了 FAM114A2,一种细胞质蛋白。FAM114A2 及其同源物 FAM114A1 的亲和层析表明,它们与高尔基体驻留膜蛋白结合,细胞质尾部的膜近端碱性残基足以进行相互作用。从 U2OS 细胞中删除这两种蛋白不会导致高尔基体功能的实质性缺陷。然而,这些蛋白质的果蝇同源物(CG9590/FAM114A)也定位在高尔基体上,并直接与 COPI 结合。缺乏 FAM114A 的果蝇突变体在唾液腺的粘性蛋白糖基化中存在缺陷。因此,FAM114A 蛋白结合高尔基体酶,是 COPI 小泡在高尔基体堆叠中再循环的特异性衔接子的候选蛋白。