The E3 ubiquitin ligase MARCH2 regulates ERGIC3-dependent trafficking of secretory proteins

• Published in: The Journal of biological chemistry Vol. 294; no. 28; pp. 10900 - 10912
• Main Authors: Yoo, Wonjin, Cho, Eun-Bee, Kim, Sungjoo, Yoon, Jong-Bok
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 12.07.2019; American Society for Biochemistry and Molecular Biology
• Subjects: cargo receptor; Carrier Proteins - metabolism; Cell Movement - physiology; E3 ubiquitin ligase; Endoplasmic Reticulum - metabolism; endoplasmic reticulum-Golgi intermediate compartment protein 3 (ERGIC3); Golgi Apparatus - metabolism; haptoglobin; HeLa Cells; Humans; intracellular trafficking; Membrane Proteins - metabolism; membrane-associated ring-CH-type finger 2 (MARCH2); protein degradation; protein secretion; Protein Synthesis and Degradation; Protein Transport; Proteolysis; Secretory Pathway; Secretory Vesicles - metabolism; ubiquitin; Ubiquitin-Protein Ligases - metabolism; Ubiquitination; α1-antitrypsin; α1-antitrypsin; endoplasmic reticulum-Golgi intermediate compartment protein 3 (ERGIC3); intracellular trafficking; E3 ubiquitin ligase; membrane-associated ring-CH-type finger 2 (MARCH2); haptoglobin; protein degradation; ubiquitin; protein secretion; cargo receptor
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.RA119.007435

The E3 ubiquitin ligase membrane-associated ring-CH–type finger 2 (MARCH2) is known to be involved in intracellular vesicular trafficking, but its role in the early secretory pathway between the endoplasmic reticulum (ER) and Golgi compartments is largely unknown. Human ER–Golgi intermediate compartment protein 2 (ERGIC2) and ERGIC3 are orthologs of Erv41 and Erv46 in yeast, proteins that form a heteromeric complex, cycle between the ER and Golgi, and function as cargo receptors in both anterograde and retrograde protein trafficking. Here, we report that MARCH2 directs ubiquitination and subsequent degradation of ERGIC3 and that MARCH2 depletion increases endogenous ERGIC3 levels. We provide evidence that the lysine residues at positions 6 and 8 of ERGIC3 are the major sites of MARCH2-mediated ubiquitination. Of note, MARCH2 did not significantly decrease the levels of an ERGIC3 variant with lysine-to-arginine substitutions at residues 6 and 8. We also show that ERGIC3 binds to itself or to ERGIC2, whereas ERGIC2 is unable to interact with itself. Our results indicate that α1-antitrypsin and haptoglobin are likely to be cargo proteins of ERGIC3. We further observed that α1-antitrypsin and haptoglobin specifically bind to ERGIC3 and that ERGIC3 depletion decreases their secretion. Moreover, MARCH2 reduced secretion of α1-antitrypsin and haptoglobin, and coexpression of the ubiquitination-resistant ERGIC3 variant largely restored their secretion, suggesting that MARCH2-mediated ERGIC3 ubiquitination is the major cause of the decrease in trafficking of ERGIC3-binding secretory proteins. Our findings provide detailed insights into the regulation of the early secretory pathway by MARCH2 and into ERGIC3 function.