The Rich World of p53 DNA Binding Targets: The Role of DNA Structure
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F19%3A00520478" target="_blank" >RIV/68081707:_____/19:00520478 - isvavai.cz</a>
Result on the web
<a href="https://www.mdpi.com/1422-0067/20/22/5605/pdf" target="_blank" >https://www.mdpi.com/1422-0067/20/22/5605/pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/ijms20225605" target="_blank" >10.3390/ijms20225605</a>
Alternative languages
Result language
angličtina
Original language name
The Rich World of p53 DNA Binding Targets: The Role of DNA Structure
Original language description
The tumor suppressor functions of p53 and its roles in regulating the cell cycle, apoptosis, senescence, and metabolism are accomplished mainly by its interactions with DNA. p53 works as a transcription factor for a significant number of genes. Most p53 target genes contain so-called p53 response elements in their promoters, consisting of 20 bp long canonical consensus sequences. Compared to other transcription factors, which usually bind to one concrete and clearly defined DNA target, the p53 consensus sequence is not strict, but contains two repeats of a 5 ' RRRCWWGYYY3 ' sequence, therefore it varies remarkably among target genes. Moreover, p53 binds also to DNA fragments that at least partially and often completely lack this consensus sequence. p53 also binds with high affinity to a variety of non-B DNA structures including Holliday junctions, cruciform structures, quadruplex DNA, triplex DNA, DNA loops, bulged DNA, and hemicatenane DNA. In this review, we summarize information of the interactions of p53 with various DNA targets and discuss the functional consequences of the rich world of p53 DNA binding targets for its complex regulatory functions.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Molecular Sciences
ISSN
1422-0067
e-ISSN
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Volume of the periodical
20
Issue of the periodical within the volume
22
Country of publishing house
CH - SWITZERLAND
Number of pages
18
Pages from-to
5605
UT code for WoS article
000502786800087
EID of the result in the Scopus database
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