Popa Stephanie, Villeneuve Julien, Stewart Sarah, Perez Garcia Esther, Petrunkina Harrison Anna, Moreau Kevin
University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, CB2 0QQ, UK.
NIHR Cambridge BRC Cell Phenotyping Hub, Department of Medicine, University of Cambridge, Cambridge, CB2 0QQ, UK.
Wellcome Open Res. 2019 Aug 9;4:119. doi: 10.12688/wellcomeopenres.15232.2. eCollection 2019.
The fundamental process of protein secretion from eukaryotic cells has been well described for many years, yet gaps in our understanding of how this process is regulated remain. With the aim of identifying novel genes involved in the secretion of glycoproteins, we used a screening pipeline consisting of a pooled genome-wide CRISPR screen, followed by secondary siRNA screening of the hits to identify and validate several novel regulators of protein secretion. We present approximately 50 novel genes not previously associated with protein secretion, many of which also had an effect on the structure of the Golgi apparatus. We further studied a small selection of hits to investigate their subcellular localisation. One of these, GPR161, is a novel Golgi-resident protein that we propose maintains Golgi structure via an interaction with golgin A5. This study has identified new factors for protein secretion involved in Golgi homeostasis.
多年来,真核细胞蛋白质分泌的基本过程已得到充分描述,但我们对该过程调控方式的理解仍存在空白。为了鉴定参与糖蛋白分泌的新基因,我们使用了一个筛选流程,包括全基因组CRISPR筛选库,随后对筛选出的命中基因进行二次siRNA筛选,以鉴定和验证几种蛋白质分泌的新型调节因子。我们展示了大约50个以前与蛋白质分泌无关的新基因,其中许多基因也对高尔基体的结构有影响。我们进一步研究了一小部分命中基因,以调查它们的亚细胞定位。其中一个基因GPR161是一种新的高尔基体驻留蛋白,我们认为它通过与高尔基体蛋白A5相互作用来维持高尔基体结构。这项研究确定了参与高尔基体稳态的蛋白质分泌新因子。