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