Pregled bibliografske jedinice broj: 256910
The role of the RecC subunit of the RecBCD enzyme in recombination and DNA repair
The role of the RecC subunit of the RecBCD enzyme in recombination and DNA repair // Abstracts of the 1st MedILS Summer School, Structure and Evolution : from Bench to Terminal
Split: Mediterranean Institute for Life Sciences, 2006. str. 43-43 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 256910 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The role of the RecC subunit of the RecBCD enzyme in recombination and DNA repair
Autori
Vlašić, Ignacija ; Ivančić-Baće, Ivana ; Salaj-Šmic, Erika ; Jeličić, Branka ; Sopta, Mary ; Brčić-Kostić, Krunoslav
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts of the 1st MedILS Summer School, Structure and Evolution : from Bench to Terminal
/ - Split : Mediterranean Institute for Life Sciences, 2006, 43-43
Skup
MedILS Summer School, Structure and Evolution : from Bench to Terminal (1 ; 2006)
Mjesto i datum
Split, Hrvatska, 18.07.2006. - 22.07.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
RecC subunit; RecBCD enzyme; recombination; DNA repair
Sažetak
The crystal structure of the RecBCD enzyme has been recently solved, which enables more precise research of the least known RecC subunit. It is already known that the N-terminal domain of the RecC subunit is required for Chi activity while the C-terminal domain is important for RecD assembly in RecBCD. To gain further insight into the importance of the RecC subunit several recC mutants have been constructed and characterized. Typical nonsense or missense mutants in the C-terminal domain of the recC gene are recombination proficient but nuclease deficient, a phenotype which mimics that of recD deletion mutations. In this study, we focused on the previously characterized recC73 mutant that has a nonfunctional C-terminal domain (deletion of T on 1938 position). In addition, we also made five new point-missense recC mutants using PCR site directed mutagenesis. According to the literature, the recC73 mutant is considered a null mutant. In contrast, we showed that the recC73 mutant is recombination proficient but only when some of the gene products from the RecF pathway are present (RecFOR and RecJ). The characterization of five additional missense recC mutants is underway.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
0098070
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Marija-Mary Sopta
(autor)
Branka Jeličić
(autor)
Krunoslav Brčić-Kostić
(autor)
Erika Salaj-Šmic
(autor)
Ignacija Vlašić
(autor)
Ivana Ivančić Baće
(autor)