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Changes in the levels of DNA methylation in testis and liver of SD rats neonatally exposed to 5‐aza‐2′‐deoxycytidine and cadmium
Author(s) -
Zhu Hongyan,
Li Keyong,
Liang Jiren,
Zhang Jie,
Wu Qing
Publication year - 2011
Publication title -
journal of applied toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 87
eISSN - 1099-1263
pISSN - 0260-437X
DOI - 10.1002/jat.1673
Subject(s) - dna methylation , methylation , microbiology and biotechnology , biology , andrology , methyltransferase , epigenetics , dna damage , dna methyltransferase , dna , gene , gene expression , biochemistry , medicine
To investigate the changes in the levels of DNA methylation in the testis during development after neonatal transient exposure to DNA methyltransferase (DNMT) inhibitors, we orally administered Sprague–Dawley (SD) rats with 5‐aza‐2′‐deoxycytidine (5‐aza‐CdR; 0.025 or 0.25 mg kg −1 ) or cadmium (Cd; 1, 2 or 4 mg kg −1 ) daily from days 3–7 postpartum (pp). Sperm numbers decreased at day 70 pp in all exposure groups. We then used a PCR‐based assay, combined bisulfite restriction analysis (COBRA) and pyrosequencing to determine the degrees of DNA methylation. Both 5‐aza‐CdR and Cd reduced DNMT activity in vivo after 5 days' exposure at day 8 pp but not at day 70 pp. In contrast, the DNA methylation level of LINE‐1 was not changed in the testis, either at day 8 pp or at day 70 pp. We observed increased apoptosis and an increase in the p53 mRNA level, accompanied by a decreased DNA methylation level in the p53 gene promoter region, at day 8 pp in testis for the 5‐aza‐CdR–exposed groups but not in the Cd‐exposed group. The Cd‐exposed group exhibited a degradation of seminiferous tubules and inhibition of a stepwise change in methylation in the coding region of c‐fos in testis at day 70 pp. Because we observed toxic phenotype development accompanied by aberrant DNA methylation, DNA methylation may play a role in chemical induced testis damage, with different DNMT inhibitors affecting DNA methylation levels in gene‐ or stage‐specific manner. Copyright © 2011 John Wiley & Sons, Ltd.