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Create and preserve: Proteostasis in development and aging is governed by Cdc48/p97/VCP
Authors:André   Franz,Leena Ackermann,Thorsten Hoppe
Affiliation:Institute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Zülpicher Straße 47a, 50674 Cologne, Germany
Abstract:The AAA-ATPase Cdc48 (also called p97 or VCP) acts as a key regulator in proteolytic pathways, coordinating recruitment and targeting of substrate proteins to the 26S proteasome or lysosomal degradation. However, in contrast to the well-known function in ubiquitin-dependent cellular processes, the physiological relevance of Cdc48 in organismic development and maintenance of protein homeostasis is less understood. Therefore, studies on multicellular model organisms help to decipher how Cdc48-dependent proteolysis is regulated in time and space to meet developmental requirements. Given the importance of developmental regulation and tissue maintenance, defects in Cdc48 activity have been linked to several human pathologies including protein aggregation diseases. Thus, addressing the underlying disease mechanisms not only contributes to our understanding on the organism-wide function of Cdc48 but also facilitates the design of specific medical therapies. In this review, we will portray the role of Cdc48 in the context of multicellular organisms, pointing out its importance for developmental processes, tissue surveillance, and disease prevention. This article is part of a Special Issue entitled: Ubiquitin–Proteasome System. Guest Editors: Thomas Sommer and Dieter H. Wolf.
Keywords:AAA, ATPase associated with diverse cellular activities   AD, Alzheimer's disease   ALS, amyotrophic lateral sclerosis   AMPK, adenosine monophosphate activated kinase   Cdc48/CDC-48, cell division cycle protein 48   DUB, de-ubiquitylating enzyme   ERAD, endoplasmic reticulum-associated degradation   HD, Huntington's disease   IBMPFD, inclusion body myopathy with Paget's disease of bone and frontotemporal dementia   MAD, mitochondria-associated degradation   MJD, Machado&ndash  Joseph disease   OMM, outer mitochondrial membrane   polyQ, extended poly-glutamine stretch   STUbL, SUMO-targeted ubiquitin ligase   TLS pol, translesional DNA polymerases   TOR, target of rapamycin   UBX, ubiquitin regulatory x   UPS, ubiquitin&ndash  proteasome system   VCP, valosin-containing protein
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