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SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection.

Authors :
Gassen NC
Niemeyer D
Muth D
Corman VM
Martinelli S
Gassen A
Hafner K
Papies J
Mösbauer K
Zellner A
Zannas AS
Herrmann A
Holsboer F
Brack-Werner R
Boshart M
Müller-Myhsok B
Drosten C
Müller MA
Rein T
Source :
Nature communications [Nat Commun] 2019 Dec 18; Vol. 10 (1), pp. 5770. Date of Electronic Publication: 2019 Dec 18.
Publication Year :
2019

Abstract

Autophagy is an essential cellular process affecting virus infections and other diseases and Beclin1 (BECN1) is one of its key regulators. Here, we identified S-phase kinase-associated protein 2 (SKP2) as E3 ligase that executes lysine-48-linked poly-ubiquitination of BECN1, thus promoting its proteasomal degradation. SKP2 activity is regulated by phosphorylation in a hetero-complex involving FKBP51, PHLPP, AKT1, and BECN1. Genetic or pharmacological inhibition of SKP2 decreases BECN1 ubiquitination, decreases BECN1 degradation and enhances autophagic flux. Middle East respiratory syndrome coronavirus (MERS-CoV) multiplication results in reduced BECN1 levels and blocks the fusion of autophagosomes and lysosomes. Inhibitors of SKP2 not only enhance autophagy but also reduce the replication of MERS-CoV up to 28,000-fold. The SKP2-BECN1 link constitutes a promising target for host-directed antiviral drugs and possibly other autophagy-sensitive conditions.

Details

Language :
English
ISSN :
2041-1723
Volume :
10
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
31852899
Full Text :
https://doi.org/10.1038/s41467-019-13659-4