Literature DB >> 9095415

Carcinogen-induced de novo methylation in c-myc exon I.

G Okada1, K Ryoyama, T Nomura, T Momoi, H Tsuchiya, T Kameyama, K Yamaguchi.   

Abstract

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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Year:  1996        PMID: 9095415     DOI: 10.7883/yoken1952.49.209

Source DB:  PubMed          Journal:  Jpn J Med Sci Biol        ISSN: 0021-5112


  1 in total

1.  Nonrandom intragenic variations in patterns of codon bias implicate a sequential interplay between transitional genetic drift and functional amino acid selection.

Authors:  K Lin; S B Tan; P R Kolatkar; R J Epstein
Journal:  J Mol Evol       Date:  2003-11       Impact factor: 2.395

  1 in total

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