Title | Mechanistic insight into the regulation of SQSTM1/p62. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Zhang Y, Mun SRan, Linares JF, Towers CG, Thorburn A, Diaz-Meco MT, Kwon YTae, Kutateladze TG |
Journal | Autophagy |
Volume | 15 |
Issue | 4 |
Pagination | 735-737 |
Date Published | 2019 04 |
ISSN | 1554-8635 |
Keywords | Autophagy, Humans, Sequestosome-1 Protein, Signal Transduction |
Abstract | SQSTM1/p62 facilitates responses to various cellular stresses and has been implicated in human diseases. This protein functions as a major cytoplasmic signaling hub and has multiple binding partners, including arginylated (Nt-R) proteins that are recognized by the ZZ domain of SQSTM1/p62 (SQSTM1/p62). We have determined the molecular mechanism of Nt-R recognition using a combination of biochemical and NMR approaches and obtained the crystal structure of SQSTM1/p62 in complex with Nt-R. We found that binding of SQSTM1/p62 to Nt-R induces SQSTM1/p62 puncta formation and macroautophagy/autophagy and identified a regulatory linker (RL) region of SQSTM1/p62 that associates with SQSTM1/p62 in vitro. Our findings suggest a mechanism for SQSTM1/p62 autoregulation that can be essential in mediating autophagy. |
DOI | 10.1080/15548627.2019.1569935 |
Alternate Journal | Autophagy |
PubMed ID | 30653391 |
PubMed Central ID | PMC6526835 |
Grant List | R01 GM125195 / GM / NIGMS NIH HHS / United States R01 GM100907 / GM / NIGMS NIH HHS / United States R01 GM106416 / GM / NIGMS NIH HHS / United States R01 CA190170 / CA / NCI NIH HHS / United States R01 CA192642 / CA / NCI NIH HHS / United States T32 CA190216 / CA / NCI NIH HHS / United States R01 CA218254 / CA / NCI NIH HHS / United States R01 CA150925 / CA / NCI NIH HHS / United States R01 GM101664 / GM / NIGMS NIH HHS / United States |
Related Faculty:
Juan Francisco Linares Rodriguez, Ph.D. Maria Diaz-Meco Conde, Ph.D.