Pregled bibliografske jedinice broj: 547667
Toxicity of thallium(I) acetate in Arabidopsis thaliana, L.
Toxicity of thallium(I) acetate in Arabidopsis thaliana, L. // 21st International Conference on Arabidopsis research, "2010 and beyond"
Yokohama, Japan, 2010. str. 100-100 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 547667 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Toxicity of thallium(I) acetate in Arabidopsis thaliana, L.
Autori
Cvjetko, Petra ; Malenica, Nenad ; Vidan, Nikolina ; Pavlica, Mirjana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
21st International Conference on Arabidopsis research, "2010 and beyond"
/ - , 2010, 100-100
Skup
21st ICAR 2010
Mjesto i datum
Yokohama, Japan, 06.06.2010. - 10.06.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Arabidopsis; thallium; genotoxicity
Sažetak
Thallium is naturally occurring trace element widely distributed in earth’s crust but at very low concentration. Due to its high toxicity to all living organisms, thallium pollution and its impact on food chain quality have become increasing environmental concerns. Increasing use in emerging new technologies and demanding high-tech industry constantly raise the concern about exposure risk to all living organisms. However, it has not been studied extensively and published toxicity studies are scarce. In order to study the toxicity effect of thallium(I) acetate, seeds of <I> Arabidopsis thaliana</I> were allowed to germinate on agar plates containing different thallium(I) acetate concentration. Following a three week dose-response assay, the inhibition of seedlings growth was proportional to the increase of thallium concentration. A random amplified polymorphic DNA (RAPD) assay was employed to detect DNA damage in response to thallium toxicity. For the DNA polymorphism analysis, sixty 10-base pair random primers with 60-70% GC content were screened. Among them, ten RAPD primers, that gave uniformly reproducible bands were chosen for further evaluation of thallium genotoxicity. Since the major drawback of the RAPD technique as a PCR-based method, is the reproducibility of the fingerprints banding, different concentration of DNA template were tested. In conclusion, after suitable optimization of PCR procedure as well as primer choice, the RAPD assay could detect DNA alteration in response to thallium exposure. These results show changes in intensity, gain and loss of bands due to thallium exposure.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
119-0982934-3110 - UČINAK ONEČIŠĆENJA NA GENETIČKU STRUKTURU ORGANIZAMA U VODENOM OKOLIŠU (Klobučar, Goran, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb