The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP

被引:2
|
作者
Koerner, Maria [1 ]
Meyer, Susanne R. [1 ]
Marincola, Gabriella [1 ,5 ]
Kern, Maximilian J. [2 ,6 ]
Grimm, Clemens [1 ]
Schuelein-Voelk, Christina [3 ]
Fischer, Utz [1 ]
Hofmann, Kay [4 ]
Buchberger, Alexander [1 ]
机构
[1] Univ Wurzburg, Chair Biochem 1, Bioctr, Wurzburg, Germany
[2] Max Planck Inst Biochem, Dept Mol Cell Biol, Martinsried, Germany
[3] Univ Wurzburg, Core Unit High Content Microscopy, Bioctr, Wurzburg, Germany
[4] Univ Cologne, Inst Genet, Cologne, Germany
[5] Lab Dr Brunner, Constance, Germany
[6] Roche Diagnost GmbH, Penzberg, Germany
来源
ELIFE | 2023年 / 12卷
关键词
p97 VCP Cdc48; ubiquitin proteasome system; nuclear import; DNA damage repair; FAM104A FLJ14775; FAM104B FLJ20434 CXorf44; Human; S; cerevisiae; HUMAN INTERACTOME; QUALITY-CONTROL; DVC1; C1ORF124; IN-VITRO; P97; UBIQUITIN; VCP; ER; DEGRADATION; CLEARANCE;
D O I
10.7554/eLife.92409
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ATPase p97 (also known as VCP, Cdc48) has crucial functions in a variety of important cellular processes such as protein quality control, organellar homeostasis, and DNA damage repair, and its de-regulation is linked to neuromuscular diseases and cancer. p97 is tightly controlled by numerous regulatory cofactors, but the full range and function of the p97-cofactor network is unknown. Here, we identify the hitherto uncharacterized FAM104 proteins as a conserved family of p97 interactors. The two human family members VCP nuclear cofactor family member 1 and 2 (VCF1/2) bind p97 directly via a novel, alpha-helical motif and associate with p97-UFD1-NPL4 and p97-UBXN2B complexes in cells. VCF1/2 localize to the nucleus and promote the nuclear import of p97. Loss of VCF1/2 results in reduced nuclear p97 levels, slow growth, and hypersensitivity to chemical inhibition of p97 in the absence and presence of DNA damage, suggesting that FAM104 proteins are critical regulators of nuclear p97 functions.
引用
收藏
页数:31
相关论文
共 23 条
  • [1] VCF1 is a p97/VCP cofactor promoting recognition of ubiquitylated p97-UFD1-NPL4 substrates
    Ann Schirin Mirsanaye
    Saskia Hoffmann
    Melanie Weisser
    Andreas Mund
    Blanca Lopez Mendez
    Dimitris Typas
    Johannes van den Boom
    Bente Benedict
    Ivo A. Hendriks
    Michael Lund Nielsen
    Hemmo Meyer
    Julien P. Duxin
    Guillermo Montoya
    Niels Mailand
    Nature Communications, 15
  • [2] VCF1 is a p97/VCP cofactor promoting recognition of ubiquitylated p97-UFD1-NPL4 substrates
    Mirsanaye, Ann Schirin
    Hoffmann, Saskia
    Weisser, Melanie
    Mund, Andreas
    Mendez, Blanca Lopez
    Typas, Dimitris
    van den Boom, Johannes
    Benedict, Bente
    Hendriks, Ivo A.
    Nielsen, Michael Lund
    Meyer, Hemmo
    Duxin, Julien P.
    Montoya, Guillermo
    Mailand, Niels
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [3] Hereditary Inclusion Body Myopathy-Linked p97/VCP Mutations in the NH2 Domain and the D1 Ring Modulate p97/VCP ATPase Activity and D2 Ring Conformation
    Halawani, Dalia
    LeBlanc, Andrea C.
    Rouiller, Isabelle
    Michnick, Stephen W.
    Servant, Marc J.
    Latterich, Martin
    MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (16) : 4484 - 4494
  • [4] VCP/p97 targets the nuclear export and degradation of p27Kip1 during G1 to S phase transition
    Shi, Xianli
    Zhu, Kaiyuan
    Ye, Zuodong
    Yue, Jianbo
    FASEB JOURNAL, 2020, 34 (04): : 5193 - 5207
  • [5] PINK1 Interacts with VCP/p97 and Activates PKA to Promote NSFL1C/p47 Phosphorylation and Dendritic Arborization in Neurons
    Wang, Kent Z. Q.
    Steer, Erin
    Otero, P. Anthony
    Bateman, Nicholas W.
    Cheng, Mary Hongying
    Scott, Ana Ligia
    Wu, Christine
    Bahar, Ivet
    Shih, Yu-Tzu
    Hsueh, Yi-Ping
    Chu, Charleen T.
    ENEURO, 2018, 5 (06)
  • [6] Specific mutations in the D1-D2 linker region of VCP/p97 enhance ATPase activity and confer resistance to VCP inhibitors
    Bastola, Prabhakar
    Wang, Feng
    Schaich, Matthew A.
    Gan, Taiping
    Freudenthal, Bret D.
    Chou, Tsui-Fen
    Chien, Jeremy
    CELL DEATH DISCOVERY, 2017, 3
  • [7] Specific mutations in the D1–D2 linker region of VCP/p97 enhance ATPase activity and confer resistance to VCP inhibitors
    Prabhakar Bastola
    Feng Wang
    Matthew A Schaich
    Taiping Gan
    Bret D Freudenthal
    Tsui-Fen Chou
    Jeremy Chien
    Cell Death Discovery, 3
  • [8] Specific mutations in the D1-D2 linker region of VCP/p97 enhance ATPase activity and confer resistance to VCP inhibitors.
    Bastola, Prabhakar
    Freudenthal, Bret
    Schaich, Matthew
    Chou, Tsui-Fen
    Gan, Taiping
    Wang, Feng
    Chien, Jeremy
    CLINICAL CANCER RESEARCH, 2018, 24 (15) : 59 - 60
  • [9] ULK1 and ULK2 Regulate Stress Granule Disassembly Through Phosphorylation and Activation of VCP/p97
    Wang, Bo
    Maxwell, Brian A.
    Joo, Joung Hyuck
    Gwon, Youngdae
    Messing, James
    Mishra, Ashutosh
    Shaw, Timothy I.
    Ward, Amber L.
    Quan, Honghu
    Sakurada, Sadie Miki
    Pruett-Miller, Shondra M.
    Bertorini, Tulio
    Vogel, Peter
    Kim, Hong Joo
    Peng, Junmin
    Taylor, J. Paul
    Kundu, Mondira
    MOLECULAR CELL, 2019, 74 (04) : 742 - +
  • [10] Role of the D1-D2 Linker of Human VCP/p97 in the Asymmetry and ATPase Activity of the D1-domain
    Tang, Wai Kwan
    Xia, Di
    SCIENTIFIC REPORTS, 2016, 6