BROMODEOXYURIDINE MUTAGENESIS, RIBONUCLEOTIDE REDUCTASE-ACTIVITY, AND DEOXYRIBONUCLEOTIDE POOLS IN HYDROXYUREA-RESISTANT MUTANTS

被引:21
作者
ASHMAN, CR
REDDY, GPV
DAVIDSON, RL
机构
[1] CHILDRENS HOSP MED CTR, DIV HUMAN GENET, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT MICROBIOL & MOLEC GENET, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, DEPT PHARMACOL, BOSTON, MA 02115 USA
[4] SIDNEY FARBER CANC INST, TUMOR BIOL LAB, BOSTON, MA 02115 USA
来源
SOMATIC CELL GENETICS | 1981年 / 7卷 / 06期
关键词
D O I
10.1007/BF01538762
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ribonucleotide reductase activity and deoxyribonucleoside triphosphate (dNTP) pools were examined in several Syrian hamster melanoma cell mutants which are resistant to hydroxyurea (HU), an inhibitor of ribonucleotide reductase, and which also show increased resistance to bromodeoxyuridine (BrdU) mutagenesis. For most of the mutants, resistance to HU and BrdU mutagenesis is associated with increased levels of ribonucleotide reductase activity. No evidence was found for qualitative alterations in the ribonucleotide reductase in the mutant cells. The dNTP pools in the mutants are somewhat resistant to the perturbations produced in wild-type cells by the addition of BrdU, although significant perturbations can be produced in the mutants by higher concentrations of BrdU. The decrease in BrdU-induced nucleotide pool perturbations may account for the resistance of the mutants to BrdU mutagenesis.
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页码:751 / 768
页数:18
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