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Pregled bibliografske jedinice broj: 387201

Genetic instability of FADD-deficient mouse cells


Matic, Igor; Furcic, Ivana; Nagy, Biserka
Genetic instability of FADD-deficient mouse cells // The European Journal of Cancer / Smyth, John (ur.).
Lyon, Francuska, 2008. str. 127-127 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Genetic instability of FADD-deficient mouse cells

Autori
Matic, Igor ; Furcic, Ivana ; Nagy, Biserka

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

Izvornik
The European Journal of Cancer / Smyth, John - , 2008, 127-127

Skup
20th European Association for Cancer Research conference

Mjesto i datum
Lyon, Francuska, 5.-8. 7. 2008

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
FADD; p53; Apoptosis; UV
(FADD; p53; Apoptoza; UV)

Sažetak
We used fibroblast cultures from the FADD-deficient mouse embryos, which were originally constructed by T.W. Mak (Toronto, Ont.) to assess directly the role of FADD, a death receptor-associated protein, in cells responses to UV radiation. These FADD-deficient fibroblasts showed much increased growth rate compared with the wild-type homozygous cells. However, the FADD - deficient fibroblasts showed the same sensitivity to UVC radiation as the wild type homozygous fibroblasts measured by MMT test. There was no difference between repair activity of UV-induced DNA damages products in the FADD - deficient and proficient cells, either. However, delay of entering S phase after UV-irradiation was reduced in the FADD-deficient cells, indicating some abnormality in the checkpoint function of the cell cycle in these deficient cells. We further analyzed changes of p53 sequences in the FADD-deficient and wild-type cells. Genomic DNA was analyzed by allele-specific polymerase chain reaction (AS-PCR) for CC to TT mutation at codons 154-155 and 175-176 in exon 5 and for C to T mutations at codons 270 and 275 in exon 8 0f the p53 gene. The mutant-specific forward primer was used for each mutation. The reverse primers for amplification of mutations were not mutant-specific. Allele-specific PCR detection of p53 in genomic DNA were analyzed by gel electrophoresis. The results showed the high frequency of changes in the mutant-specific primer for codon 270 amplified 134-base pair product from FADD deficient cell DNASs. Although frequencies of UV-induced mutations were not different between the FADD- deficient and wild-type cells, distributions and spectrum of base-substitution mutations at the p53 were different.

Izvorni jezik
Engleski

Znanstvena područja
Biologija



POVEZANOST RADA


Projekt / tema
119-0000000-1256 - Učinak ekspresije FADD-a na karcinogenezu izazvanu UV zračenjem (Inga Marijanović, )

Ustanove
Prirodoslovno-matematički fakultet, Zagreb