Aspergillus nidulans as a biological system to detect the genotoxic effects of mercury fumes on eukaryotes

G.D. Sousa, T.D. Zucchi, F.D. Zucchi, R.G. Miller, R.M.A. Anjos, P. Poli, T.M.A.D. Zucchi
Published: April 07, 2009
Genet. Mol. Res. 8 (2) : 404-413
DOI: https://doi.org/10.4238/vol8-2gmr587

Cite this Article:
G.D. Sousa, T.D. Zucchi, F.D. Zucchi, R.G. Miller, R.M.A. Anjos, P. Poli, T.M.A.D. Zucchi (2009). Aspergillus nidulans as a biological system to detect the genotoxic effects of mercury fumes on eukaryotes. Genet. Mol. Res. 8(2): 404-413. https://doi.org/10.4238/vol8-2gmr587

About the Authors
G.D. Sousa, T.D. Zucchi, F.D. Zucchi, R.G. Miller, R.M.A. AnjosM, P. Poli, T.M.A.D. Zucchi

Corresponding author
T.M.A.D. Zucchi
E-mail: tzucchi@uol.com.br.

ABSTRACT

Mercury (Hg) pollution is one of the most serious environmental problems. Due to public concern prompted by the symptoms displayed by people who consumed contaminated fish in Minamata, Japan in 1956, Hg pollution has since been kept under constant surveillance. However, despite considerable accumulation of knowledge on the noxious effects of ingested or inhaled Hg, especially for humans, there is virtually nothing known about the genotoxic effects of Hg. Because increased mitotic crossing over is assumed to be the first step leading to carcinogenesis, we used a sensitive short-term test (homozygotization index) to look for DNA alterations induced by Hg fumes. In one Aspergillus nidulans diploid strain (UT448//UT184), the effects of the Hg fumes appeared scattered all over the DNA, causing 3.05 times more recombination frequencies than the mean for other strains. Another diploid (Dp II-I//UT184) was little affected by Hg. This led us to hypothesize that a genetic factor present in the UT184 master strain genome, close to the nicB8 genetic marker, is responsible for this behavior. These findings corroborate our previous findings that the homozygotization index can be used as a bioassay for rapid and efficient assessment of ecotoxicological hazards.

Key words: mitotic crossing-over, Mercury genotoxicity, Genotoxicity detection, Homozygotization index, Ecotoxicological hazards.

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