ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.

DNA polymerase η (polη) belongs to the Y-family of DNA polymerases and facilitates translesion synthesis past UV damage. We show that, after UV irradiation, polη becomes phosphorylated at Ser601 by the ataxia-telangiectasia mutated and Rad3-related (ATR) kinase. DNA damage-induced phosphorylation of...

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Main Authors: Göhler, T, Sabbioneda, S, Green, C, Lehmann, A
Format: Journal article
Language:English
Published: 2011
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author Göhler, T
Sabbioneda, S
Green, C
Lehmann, A
author_facet Göhler, T
Sabbioneda, S
Green, C
Lehmann, A
author_sort Göhler, T
collection OXFORD
description DNA polymerase η (polη) belongs to the Y-family of DNA polymerases and facilitates translesion synthesis past UV damage. We show that, after UV irradiation, polη becomes phosphorylated at Ser601 by the ataxia-telangiectasia mutated and Rad3-related (ATR) kinase. DNA damage-induced phosphorylation of polη depends on its physical interaction with Rad18 but is independent of PCNA monoubiquitination. It requires the ubiquitin-binding domain of polη but not its PCNA-interacting motif. ATR-dependent phosphorylation of polη is necessary to restore normal survival and postreplication repair after ultraviolet irradiation in xeroderma pigmentosum variant fibroblasts, and is involved in the checkpoint response to UV damage. Taken together, our results provide evidence for a link between DNA damage-induced checkpoint activation and translesion synthesis in mammalian cells.
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spelling oxford-uuid:3298d8d5-69d1-4a3a-ba4a-0d601b6c12182022-03-26T13:15:06ZATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3298d8d5-69d1-4a3a-ba4a-0d601b6c1218EnglishSymplectic Elements at Oxford2011Göhler, TSabbioneda, SGreen, CLehmann, ADNA polymerase η (polη) belongs to the Y-family of DNA polymerases and facilitates translesion synthesis past UV damage. We show that, after UV irradiation, polη becomes phosphorylated at Ser601 by the ataxia-telangiectasia mutated and Rad3-related (ATR) kinase. DNA damage-induced phosphorylation of polη depends on its physical interaction with Rad18 but is independent of PCNA monoubiquitination. It requires the ubiquitin-binding domain of polη but not its PCNA-interacting motif. ATR-dependent phosphorylation of polη is necessary to restore normal survival and postreplication repair after ultraviolet irradiation in xeroderma pigmentosum variant fibroblasts, and is involved in the checkpoint response to UV damage. Taken together, our results provide evidence for a link between DNA damage-induced checkpoint activation and translesion synthesis in mammalian cells.
spellingShingle Göhler, T
Sabbioneda, S
Green, C
Lehmann, A
ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title_full ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title_fullStr ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title_full_unstemmed ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title_short ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage.
title_sort atr mediated phosphorylation of dna polymerase η is needed for efficient recovery from uv damage
work_keys_str_mv AT gohlert atrmediatedphosphorylationofdnapolymeraseēisneededforefficientrecoveryfromuvdamage
AT sabbionedas atrmediatedphosphorylationofdnapolymeraseēisneededforefficientrecoveryfromuvdamage
AT greenc atrmediatedphosphorylationofdnapolymeraseēisneededforefficientrecoveryfromuvdamage
AT lehmanna atrmediatedphosphorylationofdnapolymeraseēisneededforefficientrecoveryfromuvdamage