致癌物质诱导的c-myc外显子I的从头甲基化。

G Okada, K Ryoyama, T Nomura, T Momoi, H Tsuchiya, T Kameyama, K Yamaguchi
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引用次数: 2

摘要

在n -甲基-n '-硝基-n -亚硝基胍(MNNG)的响应过程中,甲基化发生在c-myc外显子I的Hpa II位点,位于P1起始位点的下游,Hpa II- pcr检测证实了这一点。Hpa II虽然位于5'侧区,但未发生甲基化。紫外线照射也导致外显子1的甲基化,甲基化程度随MNNG和紫外线剂量的增加而增加。结果表明,甲基化发生在负责致癌物的转录活性c-myc中,其机制不同于特定CpG位点的烷基化。讨论了甲基化对c-myc中发现的较少修复的可能贡献。
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Carcinogen-induced de novo methylation in c-myc exon I.

During the response of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), methylation occurred at the Hpa II site of c-myc exon I, which is located downstream of the P1 initiation site, as evidenced by the assays of Hpa II-PCR. The Hpa II spite of the 5' flanking region did not undergo methylation. UV-irradiation also led to methylation in exon I. The extent of methylation increased depending on the dose of MNNG and UV. The results suggested that methylation takes place in transcriptionally active c-myc responsible for carcinogens and is caused by mechanisms different from that of alkylation in a specific CpG site. Possible contribution of methylation to less repair found in c-myc is discussed.

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