2021
Evaluating the Influence of a G-Quadruplex Prone Sequence on the Transactivation Potential by Wild-Type and/or Mutant P53 Family Proteins through a Yeast-Based Functional Assay
MONTI, Paola; Vaclav BRAZDA; Natália BOHÁLOVÁ; Otília PORUBIAKOVÁ; Paola MENICHINI et al.Základní údaje
Originální název
Evaluating the Influence of a G-Quadruplex Prone Sequence on the Transactivation Potential by Wild-Type and/or Mutant P53 Family Proteins through a Yeast-Based Functional Assay
Autoři
MONTI, Paola; Vaclav BRAZDA; Natália BOHÁLOVÁ; Otília PORUBIAKOVÁ; Paola MENICHINI; Andrea SPECIALE; Renata BOCCIARDI; Alberto INGA a Gilberto FRONZA
Vydání
Genes, Basel, MDPI, 2021, 2073-4425
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10603 Genetics and heredity
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.141
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/21:00121141
Organizační jednotka
Přírodovědecká fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
P53 family; yeast; G-quadruplex (G4) prone sequence; wild-type and mutant P53/P63 proteins; transactivation potential
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 19. 4. 2021 17:27, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
P53, P63, and P73 proteins belong to the P53 family of transcription factors, sharing a common gene organization that, from the P1 and P2 promoters, produces two groups of mRNAs encoding proteins with different N-terminal regions; moreover, alternative splicing events at C-terminus further contribute to the generation of multiple isoforms. P53 family proteins can influence a plethora of cellular pathways mainly through the direct binding to specific DNA sequences known as response elements (REs), and the transactivation of the corresponding target genes. However, the transcriptional activation by P53 family members can be regulated at multiple levels, including the DNA topology at responsive promoters. Here, by using a yeast-based functional assay, we evaluated the influence that a G-quadruplex (G4) prone sequence adjacent to the p53 RE derived from the apoptotic PUMA target gene can exert on the transactivation potential of full-length and N-terminal truncated P53 family alpha isoforms (wild-type and mutant). Our results show that the presence of a G4 prone sequence upstream or downstream of the P53 RE leads to significant changes in the relative activity of P53 family proteins, emphasizing the potential role of structural DNA features as modifiers of P53 family functions at target promoter sites.