Počet záznamů: 1  

p73, like its p53 homolog, shows preference for inverted repeats forming cruciforms

  1. 1.
    SYSNO ASEP0492335
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    Názevp73, like its p53 homolog, shows preference for inverted repeats forming cruciforms
    Tvůrce(i) Čechová, Jana (BFU-R)
    Coufal, Jan (BFU-R) ORCID
    Jagelská, Eva (BFU-R)
    Fojta, Miroslav (BFU-R) RID, ORCID
    Brázda, Václav (BFU-R) RID, ORCID
    Celkový počet autorů5
    Číslo článkue0195835
    Zdroj.dok.PLoS ONE. - : Public Library of Science - ISSN 1932-6203
    Roč. 13, č. 4 (2018)
    Poč.str.13 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovasequence-specific binding ; dna-binding ; transcriptional activity ; supercoiled dna
    Vědní obor RIVCE - Biochemie
    Obor OECDBiochemistry and molecular biology
    CEPGA15-21855S GA ČR - Grantová agentura ČR
    EF15_003/0000477 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaBFU-R - RVO:68081707
    UT WOS000430290200060
    DOI10.1371/journal.pone.0195835
    Anotacep73 is a member of the p53 protein family and has essential functions in several signaling pathways involved in development, differentiation, DNA damage responses and cancer. As a transcription factor, p73 achieves these functions by binding to consensus DNA sequences and p73 shares at least partial target DNA binding sequence specificity with p53. Transcriptional activation by p73 has been demonstrated for more than fifty p53 targets in yeast and/or human cancer cell lines. It has also been shown previously that p53 binding to DNA is strongly dependent on DNA topology and the presence of inverted repeats that can form DNA cruciforms, but whether p73 transcriptional activity has similar dependence has not been investigated. Therefore, we evaluated p73 binding to a set of p53-response elements with identical theoretical binding affinity in their linear state, but different probabilities to form extra helical structures. We show by a yeast-based assay that transactivation in vivo correlated more with the relative propensity of a response element to form cruciforms than to its expected in vitro DNA binding affinity. Structural features of p73 target sites are therefore likely to be an important determinant of its transactivation function.
    PracovištěBiofyzikální ústav
    KontaktJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Rok sběru2019
Počet záznamů: 1  

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