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The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP
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 reg...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541173/ https://www.ncbi.nlm.nih.gov/pubmed/37713320 http://dx.doi.org/10.7554/eLife.92409 |
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author | Körner, Maria Meyer, Susanne R Marincola, Gabriella Kern, Maximilian J Grimm, Clemens Schuelein-Voelk, Christina Fischer, Utz Hofmann, Kay Buchberger, Alexander |
author_facet | Körner, Maria Meyer, Susanne R Marincola, Gabriella Kern, Maximilian J Grimm, Clemens Schuelein-Voelk, Christina Fischer, Utz Hofmann, Kay Buchberger, Alexander |
author_sort | Körner, Maria |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10541173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-105411732023-10-01 The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP Körner, Maria Meyer, Susanne R Marincola, Gabriella Kern, Maximilian J Grimm, Clemens Schuelein-Voelk, Christina Fischer, Utz Hofmann, Kay Buchberger, Alexander eLife Biochemistry and Chemical Biology 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. eLife Sciences Publications, Ltd 2023-09-15 /pmc/articles/PMC10541173/ /pubmed/37713320 http://dx.doi.org/10.7554/eLife.92409 Text en © 2023, Körner, Meyer et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Körner, Maria Meyer, Susanne R Marincola, Gabriella Kern, Maximilian J Grimm, Clemens Schuelein-Voelk, Christina Fischer, Utz Hofmann, Kay Buchberger, Alexander The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title | The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title_full | The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title_fullStr | The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title_full_unstemmed | The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title_short | The FAM104 proteins VCF1/2 promote the nuclear localization of p97/VCP |
title_sort | fam104 proteins vcf1/2 promote the nuclear localization of p97/vcp |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541173/ https://www.ncbi.nlm.nih.gov/pubmed/37713320 http://dx.doi.org/10.7554/eLife.92409 |
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