Pregled bibliografske jedinice broj: 807423
Arabidopsis thaliana MRE11 is essential for activation of cell cycle arrest, transcriptional regulation and DNA repair upon the induction of double-stranded DNA breaks
Arabidopsis thaliana MRE11 is essential for activation of cell cycle arrest, transcriptional regulation and DNA repair upon the induction of double-stranded DNA breaks // Plant biology, 18 (2016), 4; 681-694 doi:10.1111/plb.12453 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 807423 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Arabidopsis thaliana MRE11 is essential for activation of cell cycle arrest, transcriptional regulation and DNA repair upon the induction of double-stranded DNA breaks
Autori
Šamanić, Ivica ; Cvitanić, Ratko ; Simunić, Juraj ; Puizina, Jasna
Izvornik
Plant biology (1435-8603) 18
(2016), 4;
681-694
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
MRE11 ; Arabidopsis thaliana ; ATM ; double-stranded DNA breaks ; DNA damage response ; genome instability
Sažetak
Given the fundamental role of the MRE11 in many aspects of DNA metabolism and signaling in eukaryotes, we analyzed the impact of several MRE11 mutations on DNA damage response (DDR) and DNA repair in Arabidopsis thaliana. Three different atmre11 and an atatm-2 mutant lines, along with the wild-type (WT), were compared by a new -Arabidopsis genotoxic assay for in situ evaluation of the genome integrity and DNA damage repair efficiency after double strand break (DSB) induction. The results showed that, despite the phenotypic differences and the different lengths of the putative truncated AtMRE11 proteins, all three atmre11 and the atatm-2 mutant lines, exhibited common hypersensitivity to the bleomycin-treatment, upon which they reduced mitotic activities only slightly, indicating a G2/M checkpoint abrogation. In contrast to the WT which reduced the frequency of chromosomal aberrations through the recovery period after treatment, all three atmre11 and atatm-2 mutants did not recover. Moreover, atmre11-3 mutants, similarly to atatm-2 mutants, failed to transcriptionally induce several DDR genes and had altered expression of the CYCB1 ; 1::GUS protein. Nevertheless, numerous chromosomal fusions in the atmre11 mutants, observed after DNA damage induction, suggest intensive DNA repair activities. These results indicate that the functional and full-length AtMRE11 is essential for the activation of the cell cycle arrest, transcriptional regulation and the DNA repair upon the induction of DSBs.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
MZOS-177-1191196-0829 - Mehanizmi očuvanja stabilnosti genoma u viših biljaka (Puizina, Jasna, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Split
Poveznice na cjeloviti tekst rada:
doi onlinelibrary.wiley.com onlinelibrary.wiley.com pubmed.ncbi.nlm.nih.govCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE