Sequential genome-wide CRISPR-Cas9 screens identify genes regulating cell-surface expression of tetraspanins
Details
Publication Year 2023-02-28,Volume 42,Issue #2,Page 112065
Journal Title
Cell Reports
Abstract
Tetraspanins, a superfamily of membrane proteins, mediate diverse biological processes through tetraspanin-enriched microdomains in the plasma membrane. However, how their cell-surface presentation is controlled remains unclear. To identify the regulators of tetraspanin trafficking, we conduct sequential genome-wide loss-of-function CRISPR-Cas9 screens based on cell-surface expression of a tetraspanin member, TSPAN8. Several genes potentially involved in endoplasmic reticulum (ER) targeting, different biological processes in the Golgi apparatus, and protein trafficking are identified and functionally validated. Importantly, we find that biantennary N-glycans generated by MGAT1/2, but not more complex glycan structures, are important for cell-surface tetraspanin expression. Moreover, we unravel that SPPL3, a Golgi intramembrane-cleaving protease reported previously to act as a sheddase of multiple glycan-modifying enzymes, controls cell-surface tetraspanin expression through a mechanism associated with lacto-series glycolipid biosynthesis. Our study provides critical insights into the molecular regulation of cell-surface presentation of tetraspanins with implications for strategies to manipulate their functions, including cancer cell invasion.
Publisher
Cell Press
Keywords
Humans; *CRISPR-Cas Systems/genetics; Tetraspanins/genetics/metabolism; Cell Membrane/metabolism; Membrane Proteins/genetics/metabolism; *Neoplasms/genetics; CP: Cell biology; N-glycosylation; Sppl3; cancer cell invasion; endocytosis; glycosphingolipid; lacto-series glycolipid synthesis; liver cancer; protein trafficking; tetraspanin
Research Division(s)
Cancer Biology And Stem Cells
PubMed ID
36724073
Open Access at Publisher's Site
https://doi.org/10.1016/j.celrep.2023.112065
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2023-11-20 12:03:43
Last Modified: 2023-11-20 12:23:59
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