TY - JOUR
T1 - Ames test-negative carcinogen, ortho-phenyl phenol, binds tubulin and causes aneuploidy in budding yeast
AU - Nunoshiba, Tatsuo
AU - Watanabe, Eri
AU - Takahashi, Teruhisa
AU - Daigaku, Yasukazu
AU - Ishikawa, Satoko
AU - Mochizuki, Masataka
AU - Ui, Ayako
AU - Enomoto, Takemi
AU - Yamamoto, Kazuo
N1 - Funding Information:
This work was supported by a grant-in-aid from the Japanese Ministry of Education, Science, Culture, Sport and Technology, by a Research Grant from the Graduate School of Life Sciences, Tohoku University and by a Research Proposal for Long-Range Research Initiatives from the Japan Chemical Industry Association.
PY - 2007/4/1
Y1 - 2007/4/1
N2 - Ortho-phenyl phenol (OPP) is broad-spectrum of fungicides and antibacterial agents. OPP tested negative in an Ames system and positive with respect to the formation of tumors in the urinary bladder in rats when administered in diet, showing attributes of an Ames test-negative carcinogen. It has also been demonstrated that OPP does not bind or cleave DNA in vivo or in vitro, rather dose-dependent protein binding in OPP-treated rats was observed. OPP, however, generates chromosomal aberrations including aneuploidy. Thus, the steps by which Ames test-negative carcinogens exert their effects need to be elucidated. Here, we used an assay of loss of heterozygosity (LOH) in Saccharomyces cerevisiae to determine the biological effects of OPP and its hepatic metabolite phenyl hydroquinone (PHQ). LOH was found to be induced by OPP and PHQ because of a functional chromosome loss: aneuploidy. PHQ bound to and interfered with the depolymerization of tubulin in vitro and arrested the cell-cycle at M and G1. These results indicate that OPP and PHQ damaged tubulin to cause mis-segregation of chromosome by delaying cell-cycle progression through mitosis, and as a consequence caused aneuploidy.
AB - Ortho-phenyl phenol (OPP) is broad-spectrum of fungicides and antibacterial agents. OPP tested negative in an Ames system and positive with respect to the formation of tumors in the urinary bladder in rats when administered in diet, showing attributes of an Ames test-negative carcinogen. It has also been demonstrated that OPP does not bind or cleave DNA in vivo or in vitro, rather dose-dependent protein binding in OPP-treated rats was observed. OPP, however, generates chromosomal aberrations including aneuploidy. Thus, the steps by which Ames test-negative carcinogens exert their effects need to be elucidated. Here, we used an assay of loss of heterozygosity (LOH) in Saccharomyces cerevisiae to determine the biological effects of OPP and its hepatic metabolite phenyl hydroquinone (PHQ). LOH was found to be induced by OPP and PHQ because of a functional chromosome loss: aneuploidy. PHQ bound to and interfered with the depolymerization of tubulin in vitro and arrested the cell-cycle at M and G1. These results indicate that OPP and PHQ damaged tubulin to cause mis-segregation of chromosome by delaying cell-cycle progression through mitosis, and as a consequence caused aneuploidy.
KW - Ames test-negative carcinogen
KW - Aneuploidy
KW - O-phenyl phenol
KW - Phenyl hydroquinone
KW - Yeast
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U2 - 10.1016/j.mrfmmm.2007.01.002
DO - 10.1016/j.mrfmmm.2007.01.002
M3 - Article
C2 - 17289091
AN - SCOPUS:33847711832
SN - 0027-5107
VL - 617
SP - 90
EP - 97
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 1-2
ER -