Back to Search Start Over

O-methylguanine repair in liver cells in vivo: Comparison between G- and S-phase of the cell cycle.

Authors :
Rabes, H.
Kerler, R.
Rode, G.
Schuster, C.
Wilhelm, R.
Source :
Journal of Cancer Research & Clinical Oncology; 1984, Vol. 108 Issue 1, p36-45, 10p
Publication Year :
1984

Abstract

To compare the formation and persistance of alkylated DNA bases in the G- and S-phase compartments in liver in vivo, regnerating rat liver was exposed to [C]dimethylnitrosamine (0.57 mg/kg, IP injection) or N-[methyl C]- N-nitrosourea (3.3 mg/kg, intraportal injection) during the G phase of the cell cyle (12 h after partial hepatectomy), or at 24 h after partial hepatectomy with 30% hepatocytes in DNA synthesis, or at 43 h after partial hepatectomy, 4 h after an hydroxyurea block from 14 to 39 h after operation with 80% hepatocytes in DNA synthesis. At 120 min after dimethylnitrosamine and 90 s, 5, 10, or 60 min after the intraportal pulse of N-methyl- N-nitrosourea the molar fractions of 7-methylguanine (7megua), O-methylguanine (Omegua), and 3-methyladenine (3mead) and of metabolically labeled guanine were determined from DNA hydrolysates by Sephadex-G10 radiochromatography. After dimethylnitrosamine only minor differences were observed for 7megua formation in the three groups; the 3mead/7megua ratio remained constant irrespective of the number of cells in S phase. In contrast, the Omegua/7megua ratio revealed a loss of Omegua, the extent of which appeared proportional to the fraction of DNA-synthesizing cells in the liver. The rapid loss of Omegua in S-phase cells was confirmed after intraportal administration of N-methyl- N-nitrosourea. During the first 10 min after the methylnitrosourea pulse the Omegua/7megua ratio was constant in G cells and dropped from 90 s to 10 min by about 15% in liver containing 30% S-phase cells and by about 40% with 80% cells in DNA synthesis. DNA-synthesizing hepatocytes are apparently endowed with a higher Omegua DNA transferase activity than nonproliferating liver cells. The rapid, though exhaustible elimination of Omegua during S-phase might result in partial protection of DNA-synthesizing cells from base-mispairing and/or from hypomethylation at G-C sites. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01715216
Volume :
108
Issue :
1
Database :
Complementary Index
Journal :
Journal of Cancer Research & Clinical Oncology
Publication Type :
Academic Journal
Accession number :
73336308
Full Text :
https://doi.org/10.1007/BF00390971