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Linker DNA and histone contributions in nucleosome binding by p53

The tumour suppressor protein p53 regulates various genes involved in cell-cycle arrest, apoptosis and DNA repair in response to cellular stress, and apparently functions as a pioneer transcription factor. The pioneer transcription factors can bind nucleosomal DNA, where many transcription factors a...

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Autores principales: Nishimura, Masahiro, Arimura, Yasuhiro, Nozawa, Kayo, Kurumizaka, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763433/
https://www.ncbi.nlm.nih.gov/pubmed/32702132
http://dx.doi.org/10.1093/jb/mvaa081
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author Nishimura, Masahiro
Arimura, Yasuhiro
Nozawa, Kayo
Kurumizaka, Hitoshi
author_facet Nishimura, Masahiro
Arimura, Yasuhiro
Nozawa, Kayo
Kurumizaka, Hitoshi
author_sort Nishimura, Masahiro
collection PubMed
description The tumour suppressor protein p53 regulates various genes involved in cell-cycle arrest, apoptosis and DNA repair in response to cellular stress, and apparently functions as a pioneer transcription factor. The pioneer transcription factors can bind nucleosomal DNA, where many transcription factors are largely restricted. However, the mechanisms by which p53 recognizes the nucleosomal DNA are poorly understood. In the present study, we found that p53 requires linker DNAs for the efficient formation of p53-nucleosome complexes. p53 forms an additional specific complex with the nucleosome, when the p53 binding sequence is located around the entry/exit region of the nucleosomal DNA. We also showed that p53 directly binds to the histone H3-H4 complex via its N-terminal 1–93 amino acid region. These results shed light on the mechanism of nucleosome recognition by p53.
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spelling pubmed-77634332020-12-31 Linker DNA and histone contributions in nucleosome binding by p53 Nishimura, Masahiro Arimura, Yasuhiro Nozawa, Kayo Kurumizaka, Hitoshi J Biochem Regular Papers The tumour suppressor protein p53 regulates various genes involved in cell-cycle arrest, apoptosis and DNA repair in response to cellular stress, and apparently functions as a pioneer transcription factor. The pioneer transcription factors can bind nucleosomal DNA, where many transcription factors are largely restricted. However, the mechanisms by which p53 recognizes the nucleosomal DNA are poorly understood. In the present study, we found that p53 requires linker DNAs for the efficient formation of p53-nucleosome complexes. p53 forms an additional specific complex with the nucleosome, when the p53 binding sequence is located around the entry/exit region of the nucleosomal DNA. We also showed that p53 directly binds to the histone H3-H4 complex via its N-terminal 1–93 amino acid region. These results shed light on the mechanism of nucleosome recognition by p53. Oxford University Press 2020-07-23 /pmc/articles/PMC7763433/ /pubmed/32702132 http://dx.doi.org/10.1093/jb/mvaa081 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Japanese Biochemical Society. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Papers
Nishimura, Masahiro
Arimura, Yasuhiro
Nozawa, Kayo
Kurumizaka, Hitoshi
Linker DNA and histone contributions in nucleosome binding by p53
title Linker DNA and histone contributions in nucleosome binding by p53
title_full Linker DNA and histone contributions in nucleosome binding by p53
title_fullStr Linker DNA and histone contributions in nucleosome binding by p53
title_full_unstemmed Linker DNA and histone contributions in nucleosome binding by p53
title_short Linker DNA and histone contributions in nucleosome binding by p53
title_sort linker dna and histone contributions in nucleosome binding by p53
topic Regular Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763433/
https://www.ncbi.nlm.nih.gov/pubmed/32702132
http://dx.doi.org/10.1093/jb/mvaa081
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