Mechanistic insight into the regulation of SQSTM1/p62.

TitleMechanistic insight into the regulation of SQSTM1/p62.
Publication TypeJournal Article
Year of Publication2019
AuthorsZhang Y, Mun SRan, Linares JF, Towers CG, Thorburn A, Diaz-Meco MT, Kwon YTae, Kutateladze TG
JournalAutophagy
Volume15
Issue4
Pagination735-737
Date Published2019 04
ISSN1554-8635
KeywordsAutophagy, 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.

DOI10.1080/15548627.2019.1569935
Alternate JournalAutophagy
PubMed ID30653391
PubMed Central IDPMC6526835
Grant ListR01 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.

Pathology & Laboratory Medicine 1300 York Avenue New York, NY 10065 Phone: (212) 746-6464
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