Pregled bibliografske jedinice broj: 154471
The sos response signaling mechanism: possible involvement of RecA loading activity
The sos response signaling mechanism: possible involvement of RecA loading activity // Conress of the Croatian Society of Biochemistry and Molecular Biology with international participation (HDBMB 2004) : Book of Abstracts / Dumić, Jerka (ur.).
Zagreb: Farmaceutsko-biokemijski fakultet Sveučilišta u Zagrebu, 2004. str. 87-87 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 154471 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The sos response signaling mechanism: possible involvement of RecA loading activity
Autori
Ivančić-Baće, Ivana ; Vlašić, Ignacija ; Mihaljević, Boris ; Imešek, Mirna ; Salaj-Šmic, Erika ; Brčić-Kostić, Krunoslav
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Conress of the Croatian Society of Biochemistry and Molecular Biology with international participation (HDBMB 2004) : Book of Abstracts
/ Dumić, Jerka - Zagreb : Farmaceutsko-biokemijski fakultet Sveučilišta u Zagrebu, 2004, 87-87
Skup
Conress of the Croatian Society of Biochemistry and Molecular Biology with international participation
Mjesto i datum
HOC Bjelolasica, Hrvatska, 30.09.2004. - 02.10.2004
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
SOS; RecA loading; Escherichia coli
Sažetak
The SOS response involves many bacterial functions that are induced in response to damage of chromosomal DNA. The SOS response is regulated by the LexA repressor and the RecA nucleofilament which is formed at single stranded DNA. Such RecA nucleofilaments display a coprotease activity that stimulates self-cleavage of the LexA repressor. This cleavage enables transcription of more that 20 genes in the SOS pathway. Genetic analyses have shown that RecA and RecBCD are essential for SOS induction in response to double strand DNA breaks. In addition, it was shown that the SOS response is delayed in recFOR mutants. Interestingly, both enzymes, RecBCD and RecFOR, are involved in initiation of homologous recombination and both can load RecA protein on single strand DNA. We wanted to test our hypothesis that RecA loading activity is essential step in creating the SOS inducing signal. In order to test this, we measured SOS response in a strain in which the lacZ gene (expressing beta-galactosidase) is fused with the regulatory region of a sfiA SOS gene. We introduced additional mutations into this strain that inhibit RecA loading. To test whether different types of DNA damage require different enzyme processing, we measured SOS induction after UV and gama irradiation, and introduction of double strand breaks by endonuclease.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
Napomena
Rad je kao poster prezentiran i na skupu: Second Congress of Croatian Geneticists with International Participation, održanom od 24.-27.09.2005.g., Spetar, Hrvatska ; objavljen u Knjizi sažetaka ; Jasna Franekić Čolić, Đurđica Ugarković (ur.) ; Zagreb : Croatian Genetic Society, 2005. ; 80-80.
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Boris Mihaljević
(autor)
Mirna Halasz
(autor)
Krunoslav Brčić-Kostić
(autor)
Ignacija Vlašić
(autor)
Erika Salaj-Šmic
(autor)
Ivana Ivančić Baće
(autor)