溶酶体
生物
高尔基体
组织蛋白酶D
组织蛋白酶
磷酸转移酶
粘脂病
表型
细胞生物学
组织蛋白酶C
转运蛋白
酶
基因
生物化学
内质网
作者
Christopher M. Richards,Sabrina Jabs,Wenjie Qiao,Lauren D. Varanese,Michaela Schweizer,Peter Mosen,Nicholas M. Riley,Malte Klüssendorf,James Zengel,Ryan A. Flynn,Arjun Rustagi,John C. Widen,Christine E. Peters,Yaw Shin Ooi,Xuping Xie,Pei‐Yong Shi,Ralf Bartenschlager,Andreas S. Puschnik,Matthew Bogyo,Carolyn R. Bertozzi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2022-09-08
卷期号:378 (6615)
被引量:57
标识
DOI:10.1126/science.abn5648
摘要
Lysosomes are key degradative compartments of the cell. Transport to lysosomes relies on GlcNAc-1-phosphotransferase-mediated tagging of soluble enzymes with mannose 6-phosphate (M6P). GlcNAc-1-phosphotransferase deficiency leads to the severe lysosomal storage disorder mucolipidosis II (MLII). Several viruses require lysosomal cathepsins to cleave structural proteins and thus depend on functional GlcNAc-1-phosphotransferase. We used genome-scale CRISPR screens to identify lysosomal enzyme trafficking factor (LYSET, also named TMEM251) as essential for infection by cathepsin-dependent viruses including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). LYSET deficiency resulted in global loss of M6P tagging and mislocalization of GlcNAc-1-phosphotransferase from the Golgi complex to lysosomes.
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