Detailed Information on Publication Record
2020
The Influence of Quadruplex Structure in Proximity to P53 Target Sequences on the Transactivation Potential of P53 Alpha Isoforms
PORUBIAKOVÁ, Otília, Natália BOHÁLOVÁ, Alberto INGA, Natália VADOVIČOVÁ, Jan COUFAL et. al.Basic information
Original name
The Influence of Quadruplex Structure in Proximity to P53 Target Sequences on the Transactivation Potential of P53 Alpha Isoforms
Authors
PORUBIAKOVÁ, Otília (703 Slovakia), Natália BOHÁLOVÁ (703 Slovakia, belonging to the institution), Alberto INGA (380 Italy), Natália VADOVIČOVÁ (203 Czech Republic, belonging to the institution), Jan COUFAL (203 Czech Republic), Miroslav FOJTA (203 Czech Republic) and Václav BRÁZDA (203 Czech Republic, guarantor)
Edition
International Journal of Molecular Sciences, Basel, Molecular Diversity Preservation International, 2020, 1422-0067
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.923
RIV identification code
RIV/00216224:14310/20:00115260
Organization unit
Faculty of Science
UT WoS
000515378000127
Keywords in English
p53 protein; protein-DNA interaction; transactivation potential
Tags
International impact, Reviewed
Změněno: 31/8/2021 16:32, Mgr. Marie Šípková, DiS.
Abstract
V originále
p53 is one of the most studied tumor suppressor proteins that plays an important role in basic biological processes including cell cycle, DNA damage response, apoptosis, and senescence. The human TP53 gene contains alternative promoters that produce N-terminally truncated proteins and can produce several isoforms due to alternative splicing. p53 function is realized by binding to a specific DNA response element (RE), resulting in the transactivation of target genes. Here, we evaluated the influence of quadruplex DNA structure on the transactivation potential of full-length and N-terminal truncated p53 alpha isoforms in a panel of S. cerevisiae luciferase reporter strains. Our results show that a G-quadruplex prone sequence is not sufficient for transcription activation by p53 alpha isoforms, but the presence of this feature in proximity to a p53 RE leads to a significant reduction of transcriptional activity and changes the dynamics between co-expressed p53 alpha isoforms.