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Pregled bibliografske jedinice broj: 678857

Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis


Zorić, Arijana; Horvat, Anđela; Slade, Neda.
Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis // 6th p63/p73 International Workshop / Nakagawara, Akira (ur.).
Chiba, 2013. str. 57-57 (poster, nije recenziran, sažetak, ostalo)


CROSBI ID: 678857 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis

Autori
Zorić, Arijana ; Horvat, Anđela ; Slade, Neda.

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Izvornik
6th p63/p73 International Workshop / Nakagawara, Akira - Chiba, 2013, 57-57

Skup
6th p63/p73 International Workshop at Kasuza Akademia Park in Chiba, Japan

Mjesto i datum
Chiba, Japan, 15.09.2013. - 18.09.2013

Vrsta sudjelovanja
Poster

Vrsta recenzije
Nije recenziran

Ključne riječi
mutant p53; p63; p73

Sažetak
The p53 activities are due, at least in part, to its ability to form oligomers that bind to specific DNA sequences and activate transcription. Since some mutant p53 proteins and ΔNp73 isoforms form heterocomplexes with TAp73, we asked whether p53 isoforms can do the same and potentially act as dominant- negative inhibitors of TAp73. Moreover, it has already been found that some isoforms form complex with wtp53 and some of them inhibit p53 tumor-suppressor functions. Therefore, we studied the complex formation and co- immunoprecipitation assays show that all six p53 isoforms examined can form complexes with TAp73β, whereas only Δ133p53α/β/γ isoforms form complex with TAp73α. All p53 isoforms counteract TAp73β transactivation function but with different efficiency and in a promoter- dependent manner. Furthermore, apoptotic activity of TAp73β was augmented by coexpression of p53β, whereas Δ133p53α and β inhibit its apoptotic activity most efficiently. We have determined the half-life of different p53 isoforms: p53γ isoform has the shortest half-life, whereas Δ133p53γ has the longest half-life. Inhibitory interactions of two proteins in complex often lead to their stabilization. However, only three isoforms (Δ133p53α, Δ133p53β and Δ40p53α) stabilize TAp73β. We are convinced that defining the interactions between p53/p73 would give a new insight into how the p53 isoforms modulate the p73 functions in tumorigenesis.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
098-0982464-2391 - Uloga mreže proteina p53/p73 u sarkomima mekih tkiva čovjeka (Slade, Neda, MZOS ) ( CroRIS)

Ustanove:
Institut "Ruđer Bošković", Zagreb

Profili:

Avatar Url Neda Slade (autor)

Avatar Url Arijana Zorić (autor)

Avatar Url Anđela Horvat (autor)


Citiraj ovu publikaciju:

Zorić, Arijana; Horvat, Anđela; Slade, Neda.
Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis // 6th p63/p73 International Workshop / Nakagawara, Akira (ur.).
Chiba, 2013. str. 57-57 (poster, nije recenziran, sažetak, ostalo)
Zorić, A., Horvat, A. & Slade, N. (2013) Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis. U: Nakagawara, A. (ur.)6th p63/p73 International Workshop.
@article{article, author = {Zori\'{c}, Arijana and Horvat, An\djela and Slade, Neda.}, editor = {Nakagawara, A.}, year = {2013}, pages = {57-57}, keywords = {mutant p53, p63, p73}, title = {Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis}, keyword = {mutant p53, p63, p73}, publisherplace = {Chiba, Japan} }
@article{article, author = {Zori\'{c}, Arijana and Horvat, An\djela and Slade, Neda.}, editor = {Nakagawara, A.}, year = {2013}, pages = {57-57}, keywords = {mutant p53, p63, p73}, title = {Mutant p53 impact TAp73beta and TAp63alpha transcriptional activity and apoptosis}, keyword = {mutant p53, p63, p73}, publisherplace = {Chiba, Japan} }




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