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Ubiquitin Ligase SYVN1/HRD1 Facilitates Degradation of the SERPINA1 Z Variant/α-1-antitrypsin Z Variant Via SQSTM1/p62-dependent Selective Autophagy

Overview
Journal Autophagy
Specialty Cell Biology
Date 2017 Jan 26
PMID 28121484
Citations 37
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Abstract

SERPINA1/AAT/α-1-antitrypsin (serpin family A member 1) deficiency (SERPINA1/ AAT-D) is an autosomal recessive disorder characterized by the retention of misfolded SERPINA1/AAT in the endoplasmic reticulum (ER) of hepatocytes and a significant reduction of serum SERPINA1/AAT level. The Z variant of SERPINA1/AAT, containing a Glu342Lys (E342K) mutation (SERPINA1/ATZ), the most common form of SERPINA1/AAT-D, is prone to misfolding and polymerization, which retains it in the ER of hepatocytes and leads to liver injury. Both proteasome and macroautophagy/autophagy pathways are responsible for disposal of SERPINA1/ATZ after it accumulates in the ER. However, the mechanisms by which SERPINA1/ATZ is selectively degraded by autophagy remain unknown. Here, we showed that ER membrane-spanning ubiquitin ligase (E3) SYVN1/HRD1 enhances the degradation of SERPINA1/ATZ through the autophagy-lysosome pathway. We found that SYVN1 promoted SERPINA1/ATZ, especially Triton X 100-insoluble SERPINA1/ATZ clearance. However, the effect of SYVN1 in SERPINA1/ATZ clearance was impaired after autophagy inhibition, as well as in autophagy-related 5 (atg5) knockout cells. On the contrary, autophagy induction enhanced SYVN1-mediated SERPINA1/ATZ degradation. Further study showed that SYVN1 mediated SERPINA1/ATZ ubiquitination, which is required for autophagic degradation of SERPINA1/ATZ by promoting the interaction between SERPINA1/ATZ and SQSTM1/p62 for formation of the autophagy complex. Interestingly, SYVN1-mediated lysine 48 (K48)-linked polyubiquitin chains that conjugated onto SERPINA1/ATZ might predominantly bind to the ubiquitin-associated (UBA) domain of SQSTM1 and couple the ubiquitinated SERPINA1/ATZ to the lysosome for degradation. In addition, autophagy inhibition attenuated the suppressive effect of SYVN1 on SERPINA1/ATZ cytotoxicity, and the autophagy inducer rapamycin enhanced the suppressive effect of SYVN1 on SERPINA1/ATZ-induced cell apoptosis. Therefore, this study proved that SYVN1 enhances SERPINA1/ATZ degradation through SQSTM1-dependent autophagy and attenuates SERPINA1/ATZ cytotoxicity.

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References
1.
Di X, Wang Y, Han D, Fu Y, Duerfeldt A, Blagg B . Grp94 Protein Delivers γ-Aminobutyric Acid Type A (GABAA) Receptors to Hrd1 Protein-mediated Endoplasmic Reticulum-associated Degradation. J Biol Chem. 2016; 291(18):9526-39. PMC: 4850292. DOI: 10.1074/jbc.M115.705004. View

2.
Teckman J, Burrows J, Hidvegi T, Schmidt B, Hale P, Perlmutter D . The proteasome participates in degradation of mutant alpha 1-antitrypsin Z in the endoplasmic reticulum of hepatoma-derived hepatocytes. J Biol Chem. 2001; 276(48):44865-72. DOI: 10.1074/jbc.M103703200. View

3.
Finley D . Recognition and processing of ubiquitin-protein conjugates by the proteasome. Annu Rev Biochem. 2009; 78:477-513. PMC: 3431160. DOI: 10.1146/annurev.biochem.78.081507.101607. View

4.
Liu Z, Chen P, Gao H, Gu Y, Yang J, Peng H . Ubiquitylation of autophagy receptor Optineurin by HACE1 activates selective autophagy for tumor suppression. Cancer Cell. 2014; 26(1):106-20. PMC: 4166492. DOI: 10.1016/j.ccr.2014.05.015. View

5.
Eriksson S, Carlson J, Velez R . Risk of cirrhosis and primary liver cancer in alpha 1-antitrypsin deficiency. N Engl J Med. 1986; 314(12):736-9. DOI: 10.1056/NEJM198603203141202. View