Affiliation:
1. Laboratory of Chromatin Structure and Function, Institute for Quantitative Biosciences
2. Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan
Abstract
Abstract
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.
Funder
Japan Society for the Promotion of Science
JSPS
KAKENHI
Japan Science and Technology Agency
Precursory Research for Embryonic Science and Technology
PRESTO
Platform Project for Supporting Drug Discovery and Life Science Research
Japan Agency for Medical Research and Development
JST Exploratory Research for Advanced Technology
JSPS Research Fellowship for Young Scientists
Publisher
Oxford University Press (OUP)
Subject
Molecular Biology,Biochemistry,General Medicine
Cited by
18 articles.
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