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STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation
The ATM (ataxia-telangiectasia mutated) kinase is rapidly activated following DNA damage and phosphorylates its downstream targets to launch DDR signaling. Recently, we and others showed that UFM1 signaling promotes ATM activation. We further discovered that monoufmylation of histone H4 at Lys(31) b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269669/ https://www.ncbi.nlm.nih.gov/pubmed/32537488 http://dx.doi.org/10.1126/sciadv.aax8214 |
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author | Qin, Bo Yu, Jia Nowsheen, Somaira Zhao, Fei Wang, Liewei Lou, Zhenkun |
author_facet | Qin, Bo Yu, Jia Nowsheen, Somaira Zhao, Fei Wang, Liewei Lou, Zhenkun |
author_sort | Qin, Bo |
collection | PubMed |
description | The ATM (ataxia-telangiectasia mutated) kinase is rapidly activated following DNA damage and phosphorylates its downstream targets to launch DDR signaling. Recently, we and others showed that UFM1 signaling promotes ATM activation. We further discovered that monoufmylation of histone H4 at Lys(31) by UFM1-specific ligase 1 (UFL1) is an important step in the amplification of ATM activation. However, how monoufmylated H4 enhances ATM activation is still unknown. Here, we report STK38, a kinase in the Hippo pathway, serves as a reader for histone H4 ufmylation to promote ATM activation in a kinase-independent manner. STK38 contains a potential UFM1 binding motif which recognizes ufmylated H4 and recruits the SUV39H1 to the double-strand breaks, resulting in H3K9 trimethylation and Tip60 activation to promote ATM activation. Together, STK38 is a previously unknown player in DNA damage signaling and functions as a reader of monoufmylated H4 at Lys(31) to promote ATM activation. |
format | Online Article Text |
id | pubmed-7269669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72696692020-06-11 STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation Qin, Bo Yu, Jia Nowsheen, Somaira Zhao, Fei Wang, Liewei Lou, Zhenkun Sci Adv Research Articles The ATM (ataxia-telangiectasia mutated) kinase is rapidly activated following DNA damage and phosphorylates its downstream targets to launch DDR signaling. Recently, we and others showed that UFM1 signaling promotes ATM activation. We further discovered that monoufmylation of histone H4 at Lys(31) by UFM1-specific ligase 1 (UFL1) is an important step in the amplification of ATM activation. However, how monoufmylated H4 enhances ATM activation is still unknown. Here, we report STK38, a kinase in the Hippo pathway, serves as a reader for histone H4 ufmylation to promote ATM activation in a kinase-independent manner. STK38 contains a potential UFM1 binding motif which recognizes ufmylated H4 and recruits the SUV39H1 to the double-strand breaks, resulting in H3K9 trimethylation and Tip60 activation to promote ATM activation. Together, STK38 is a previously unknown player in DNA damage signaling and functions as a reader of monoufmylated H4 at Lys(31) to promote ATM activation. American Association for the Advancement of Science 2020-06-03 /pmc/articles/PMC7269669/ /pubmed/32537488 http://dx.doi.org/10.1126/sciadv.aax8214 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Qin, Bo Yu, Jia Nowsheen, Somaira Zhao, Fei Wang, Liewei Lou, Zhenkun STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title | STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title_full | STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title_fullStr | STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title_full_unstemmed | STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title_short | STK38 promotes ATM activation by acting as a reader of histone H4 ufmylation |
title_sort | stk38 promotes atm activation by acting as a reader of histone h4 ufmylation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269669/ https://www.ncbi.nlm.nih.gov/pubmed/32537488 http://dx.doi.org/10.1126/sciadv.aax8214 |
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