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

Koerner, M., Meyer, S. R., Marincola, G., Kern, M., Grimm, C., Schuelein-Voelk, C., et al. (2023). The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP. eLife, 12: e92409. doi:10.7554/eLife.92409.

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 Creators:
Koerner, Maria1, Author
Meyer, Susanne R.1, Author
Marincola, Gabriella1, Author
Kern, Maximilian2, Author           
Grimm, Clemens1, Author
Schuelein-Voelk, Christina1, Author
Fischer, Utz1, Author
Hofmann, Kay1, Author
Buchberger, Alexander1, Author
Affiliations:
1external, ou_persistent22              
2Jentsch, Stefan / Molecular Cell Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565156              

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Free keywords: HUMAN INTERACTOME; QUALITY-CONTROL; DVC1 C1ORF124; IN-VITRO; P97; UBIQUITIN; VCP; ER; DEGRADATION; CLEARANCELife Sciences & Biomedicine - Other Topics; p97 VCP Cdc48; ubiquitin proteasome system; nuclear import; DNA damage repair; FAM104A FLJ14775; FAM104B FLJ20434 CXorf44; Human; S; cerevisiae;
 Abstract: 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.

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Language(s): eng - English
 Dates: 2023-09-15
 Publication Status: Published online
 Pages: 31
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 001078232900001
DOI: 10.7554/eLife.92409
 Degree: -

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Title: eLife
Source Genre: Journal
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Publ. Info: Cambridge : eLife Sciences Publications
Pages: - Volume / Issue: 12 Sequence Number: e92409 Start / End Page: - Identifier: Other: URL
ISSN: 2050-084X
CoNE: https://pure.mpg.de/cone/journals/resource/2050-084X