SPRTN patient variants cause global-genome DNA-protein crosslink repair defects

DNA-protein crosslinks (DPCs) are toxic DNA lesions which threaten genome stability. Here, the authors develop a method to track the fate of DPCs in cells and identify a role for the SPRTN protease in replication-independent DPC repair.

Bibliographic Details
Main Authors: Pedro Weickert, Hao-Yi Li, Maximilian J. Götz, Sophie Dürauer, Denitsa Yaneva, Shubo Zhao, Jacqueline Cordes, Aleida C. Acampora, Ignasi Forne, Axel Imhof, Julian Stingele
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-35988-1
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author Pedro Weickert
Hao-Yi Li
Maximilian J. Götz
Sophie Dürauer
Denitsa Yaneva
Shubo Zhao
Jacqueline Cordes
Aleida C. Acampora
Ignasi Forne
Axel Imhof
Julian Stingele
author_facet Pedro Weickert
Hao-Yi Li
Maximilian J. Götz
Sophie Dürauer
Denitsa Yaneva
Shubo Zhao
Jacqueline Cordes
Aleida C. Acampora
Ignasi Forne
Axel Imhof
Julian Stingele
author_sort Pedro Weickert
collection DOAJ
description DNA-protein crosslinks (DPCs) are toxic DNA lesions which threaten genome stability. Here, the authors develop a method to track the fate of DPCs in cells and identify a role for the SPRTN protease in replication-independent DPC repair.
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spelling doaj.art-dc7e3a77ff704d98b30b8ecc3d84505f2023-01-22T12:19:21ZengNature PortfolioNature Communications2041-17232023-01-0114111410.1038/s41467-023-35988-1SPRTN patient variants cause global-genome DNA-protein crosslink repair defectsPedro Weickert0Hao-Yi Li1Maximilian J. Götz2Sophie Dürauer3Denitsa Yaneva4Shubo Zhao5Jacqueline Cordes6Aleida C. Acampora7Ignasi Forne8Axel Imhof9Julian Stingele10Department of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityProtein Analysis Unit (ZfP), BioMedical Center (BMC), Ludwig-Maximilians-UniversityProtein Analysis Unit (ZfP), BioMedical Center (BMC), Ludwig-Maximilians-UniversityDepartment of Biochemistry, Ludwig-Maximilians-UniversityDNA-protein crosslinks (DPCs) are toxic DNA lesions which threaten genome stability. Here, the authors develop a method to track the fate of DPCs in cells and identify a role for the SPRTN protease in replication-independent DPC repair.https://doi.org/10.1038/s41467-023-35988-1
spellingShingle Pedro Weickert
Hao-Yi Li
Maximilian J. Götz
Sophie Dürauer
Denitsa Yaneva
Shubo Zhao
Jacqueline Cordes
Aleida C. Acampora
Ignasi Forne
Axel Imhof
Julian Stingele
SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
Nature Communications
title SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
title_full SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
title_fullStr SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
title_full_unstemmed SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
title_short SPRTN patient variants cause global-genome DNA-protein crosslink repair defects
title_sort sprtn patient variants cause global genome dna protein crosslink repair defects
url https://doi.org/10.1038/s41467-023-35988-1
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