Ubiquitination of UVRAG by SMURF1 promotes autophagosome maturation and inhibits hepatocellular carcinoma growth.

Abstract

UVRAG (UV radiation resistance associated) is an important regulator of mammalian macroautophagy/autophagy by interacting with BECN1, PIK3C3, and RUBCN. Phosphorylation of UVRAG by MTORC1 negatively regulates autophagosome maturation under nutrient-enriched conditions. However, how UVRAG ubiquitination is regulated is still unknown. Here we report that UVRAG is ubiquitinated by SMURF1 at lysine residues 517 and 559, which decreases the association of UVRAG with RUBCN and promotes autophagosome maturation. However, the deubiquitinase ZRANB1 specifically cleaves SMURF1-induced K29 and K33-linked polyubiquitin chains from UVRAG, thereby increasing the binding of UVRAG to RUBCN and inhibiting autophagy flux. We also demonstrate that CSNK1A1-mediated UVRAG phosphorylation at Ser522 disrupts the binding of SMURF1 to UVRAG through PPxY motif and blocks UVRAG ubiquitination-mediated autophagosome maturation. Interestingly, ZRANB1 is phosphorylated at Thr35, and Ser209 residues by CSNK1A1, and this phosphorylation activates its deubiquitinating activity. Importantly, we provide in vitro and in vivo evidence that UVRAG ubiquitination at lysine residues 517 and 559 or prevention of Ser522 phosphorylation by D4476, a CSNK1A1 inhibitor, enhances the lysosomal degradation of EGFR, which significantly inhibits hepatocellular carcinoma (HCC) growth. Furthermore, UVRAG S522 phosphorylation levels correlate with ZRANB1 T35/S209 phosphorylation levels and poor prognosis in HCC patients. These findings identify a novel molecular mechanism by which ubiquitination and phosphorylation of UVRAG regulate its function in autophagosome maturation and HCC growth, encouraging further study of their potential therapeutic implications. Abbreviations: ATG: autophagy related; BafA1: bafilomycin A1; BECN1: beclin 1; CHX: cycloheximide; CSNK1A1/CK1α: casein kinase 1 alpha 1; CQ: chloroquine; DUB: deubiquitinase; EBSS: Earle's balanced salt solution; EGF: epidermal growth factor; GFP: green fluorescent protein; GST: glutathione S-transferase; HBSS: Hanks balanced salts solution; HCC: hepatocellular carcinoma; MAP1LC3B/LC3: microtubule associated protein 1 light chain 3 beta; MEFs: mouse embryo fibroblasts; mRFP: monomeric red fluorescent protein; PIK3C3/VPS34: phosphatidylinositol 3-kinase catalytic subunit type 3; PTMs: post-translational modifications; RUBCN: rubicon autophagy regulator; siRNA: small interfering RNA; SMURF1: SMAD specific E3 ubiquitin protein ligase 1; SQSTM1: sequestosome 1; Ub-AMC: ubiquitin-7-amido-4-methylcoumarin: a fluorogenic substrate; UVRAG: UV radiation resistance associated; ZRANB1/TRABID: zinc finger RANBP2-type containing 1.

• Authors: Xing Feng, Yanyan Jia, Yuyu Zhang, Fei Ma, Yuekun Zhu, Xuehui Hong, Qingxin Zhou, Ruixing He, Heng Zhang, Junfei Jin, Daxun Piao, He Huang, Qinghua Li, Xingfeng Qiu, Zhiyong Zhang
• Journal: Autophagy (Autophagy) Vol. 15 Issue 7 Pg. 1130-1149 (07 2019) ISSN: 1554-8635 [Electronic] United States
• PMID: 30686098 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Tumor Suppressor Proteins
• UVRAG protein, human
• Ubiquitin
• SMURF1 protein, human
• Ubiquitin-Protein Ligases
• EGFR protein, human
• ErbB Receptors
• CSNK1A1 protein, human
• Casein Kinase Ialpha
• Endopeptidases
• ZRANB1 protein, human
• Deubiquitinating Enzymes
• Ubiquitin Thiolesterase
• Ubiquitin-Specific Proteases

Topics

• Amino Acid Motifs (genetics)
• Animals
• Autophagosomes (metabolism)
• Carcinoma, Hepatocellular (genetics, metabolism, mortality)
• Casein Kinase Ialpha (genetics, metabolism)
• Deubiquitinating Enzymes (metabolism)
• Endopeptidases
• ErbB Receptors (metabolism)
• HEK293 Cells
• Humans
• Liver Neoplasms (genetics, metabolism, mortality)
• Mice
• Mice, Inbred BALB C
• Mice, Nude
• Mutation
• Phosphorylation
• Prognosis
• Protein Processing, Post-Translational (genetics)
• Transplantation, Heterologous
• Tumor Suppressor Proteins (chemistry, genetics, metabolism)
• Ubiquitin (metabolism)
• Ubiquitin Thiolesterase (metabolism)
• Ubiquitin-Protein Ligases (antagonists & inhibitors, genetics, metabolism)
• Ubiquitin-Specific Proteases (metabolism)
• Ubiquitination (genetics)