|This article relies largely or entirely on a single source. (December 2014)|
6-Methoxyguanine; O6-Methylguanine; 2-Amino-6-methoxypurine
3D model (JSmol)
|Molar mass||165.16 g·mol−1|
|Melting point||>300 °C|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
6-O-Methylguanine is a derivative of the nucleobase guanine in which a methyl group is attached to the oxygen atom. It base-pairs to thymine rather than cytosine, causing a G:C to A:T transition in DNA.
6-O-methylguanine is formed in DNA by alkylation of the oxygen atom of guanine, most often by N-nitroso compounds (NOC) and sometimes due to methylation by other compounds such as endogenous S-adenosyl methionine. NOC are alkylating agents formed by the reaction of nitrite or other nitrogen oxides with secondary amines and N-alkylamides, yielding N-alkylnitrosamines and N-alkylnitrosamides.
NOC are found in some foods (bacon, sausages, cheese) and tobacco smoke, and are formed in the gastrointestinal tract, especially after consumption of red meat. In addition, endogenous nitric oxide levels were found to be enhanced under chronic inflammatory conditions, and this could favor NOC formation in the large intestine.
Repair and carcinogenicity
Repair of 6-O-methylguanine in DNA is primarily carried out by O-6-methylguanine-DNA methyltransferase (MGMT). Epigenetic reductions in MGMT expression are one of the most frequent DNA repair defects, associated with carcinogenesis. (Also see MGMT expression in cancer.)
In 1985 Yarosh summarized the early work that established 6-O-methylguanine as the alkylated base in DNA that was the most mutagenic and carcinogenic. In 1994 Rasouli-Nia et al. showed that about one mutation was induced for every eight unrepaired 6-O-Methylguanines in DNA.
About 1/3rd of the time 6-O-methylguanine mispairs during replication, leading to the incorporation of dTMP rather than dCMP. 6-O-methylguanine is therefore a mutagenic nucleobase. However, the mutagenicity of a particular 6-O-methylguanine base depends on the sequence in which it is embedded.
Unrepaired 6-O-methylguanine can also lead to cell cycle arrest, sister chromatid exchange, or apoptosis. These effects are due to interaction of the DNA mismatch repair pathway with 6-O-methylguanine, and also depend on signaling network activation, led by early ATM, H2AX, CHK1 and p53 phosphorylation.
- 6-O-Methylguanine at Sigma-Aldrich
- Fahrer J, Kaina B (2013). "O6-methylguanine-DNA methyltransferase in the defense against N-nitroso compounds and colorectal cancer". Carcinogenesis. 34 (11): 2435–42. PMID 23929436. doi:10.1093/carcin/bgt275.
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- Abbott PJ, Saffhill R (1979). "DNA synthesis with methylated poly(dC-dG) templates. Evidence for a competitive nature to miscoding by O(6)-methylguanine". Biochim. Biophys. Acta. 562 (1): 51–61. PMID 373805. doi:10.1016/0005-2787(79)90125-4.
- Georgiadis P, Smith CA, Swann PF (1991). "Nitrosamine-induced cancer: selective repair and conformational differences between O6-methylguanine residues in different positions in and around codon 12 of rat H-ras". Cancer Res. 51 (21): 5843–50. PMID 1933853.
- Noonan EM, Shah D, Yaffe MB, Lauffenburger DA, Samson LD (2012). "O6-Methylguanine DNA lesions induce an intra-S-phase arrest from which cells exit into apoptosis governed by early and late multi-pathway signaling network activation". Integr Biol (Camb). 4 (10): 1237–55. PMC . PMID 22892544. doi:10.1039/c2ib20091k.
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