TEMPERATURE-SENSITIVE DNA MUTANT OF CHINESE-HAMSTER OVARY CELLS WITH A THERMOLABILE RIBONUCLEOTIDE REDUCTASE-ACTIVITY

被引:5
作者
WOJCIK, BE
DERMODY, JJ
OZER, HL
MUN, B
MATHEWS, CK
机构
[1] CUNY HUNTER COLL,DEPT BIOL SCI,NEW YORK,NY 10021
[2] UNIV MED & DENT NEW JERSEY,NEW JERSEY MED SCH,DEPT MICROBIOL & MOLEC GENET,NEWARK,NJ 07103
[3] OREGON STATE UNIV,DEPT BIOCHEM & BIOPHYS,CORVALLIS,OR 97331
关键词
D O I
10.1128/MCB.10.11.5688
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
JB3-B is a Chinese hamster ovary cell mutant previously shown to be temperature sensitive for DNA replication (J.J. Dermody, B.E. Wojcik, H. Du, and H.L. Ozer, Mol. Cell. Biol. 6: 4594-4601, 1986). It was chosen for detailed study because of its novel property of inhibiting both polyomavirus and adenovirus DNA synthesis in a temperature-dependent manner. Pulse-labeling studies demonstrated a defect in the rate of adenovirus DNA synthesis. Measurement of deoxyribonucleoside triphosphate (dNTP) pools as a function of time after shift of uninfected cultures from 33 to 39°C revealed that all four dNTP pools declined at similar rates in extracts prepared either from whole cells or from rapidly isolated nuclei. Ribonucleoside triphosphate pools were unaffected by a temperature shift, ruling out the possibility that the mutation affects nucleoside diphosphokinase. However, ribonucleotide reductase activity, as measured in extracts, declined after cell cultures underwent a temperature shift, in parallel with the decline in dNTP pool sizes. Moreover, the activity of cell extracts was thermolabile in vitro, consistent with the model that the JB3-B mutation affects the structural gene for one of the ribonucleotide reductase subunits. The kinetics of dNTP pool size changes after temperature shift are quite distinct from those reported after inhibition of ribonucleotide reductase with hydroxyurea. An indirect effect on ribonucleotide reductase activity in JB3-B has not been excluded since human sequences other than those encoding the enzyme subunits can correct the temperature-sensitive growth defect in the mutant.
引用
收藏
页码:5688 / 5699
页数:12
相关论文
共 48 条
[11]   INSITU ENZYMOLOGY OF DNA-REPLICATION AND ULTRAVIOLET-INDUCED DNA-REPAIR SYNTHESIS IN PERMEABLE HUMAN-CELLS [J].
DRESLER, SL ;
FRATTINI, MG ;
ROBINSONHILL, RM .
BIOCHEMISTRY, 1988, 27 (19) :7247-7254
[12]  
EKI T, 1990, J BIOL CHEM, V265, P26
[13]   DEOXYRIBONUCLEOSIDE TRIPHOSPHATE METABOLISM AND THE MAMMALIAN-CELL CYCLE - EFFECTS OF HYDROXYUREA ON MUTANT AND WILD-TYPE MOUSE S49 T-LYMPHOMA CELLS [J].
ERIKSSON, S ;
SKOG, S ;
TRIBUKAIT, B ;
WALLSTROM, B .
EXPERIMENTAL CELL RESEARCH, 1987, 168 (01) :79-88
[14]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[15]   RAPID AND SENSITIVE HIGH-PRESSURE LIQUID-CHROMATOGRAPHY ASSAY FOR DEOXYRIBONUCLEOSIDE TRIPHOSPHATES IN CELL-EXTRACTS [J].
GARRETT, C ;
SANTI, DV .
ANALYTICAL BIOCHEMISTRY, 1979, 99 (02) :268-273
[16]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467
[17]  
GRINDEY GB, 1980, MOL PHARMACOL, V17, P256
[18]   UBIQUITOUS, INTERSPERSED REPEATED SEQUENCES IN MAMMALIAN GENOMES [J].
JELINEK, WR ;
TOOMEY, TP ;
LEINWAND, L ;
DUNCAN, CH ;
BIRO, PA ;
CHOUDARY, PV ;
WEISSMAN, SM ;
RUBIN, CM ;
HOUCK, CM ;
DEININGER, PL ;
SCHMID, CW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (03) :1398-1402
[19]   TEMPERATURE-SENSITIVE MUTANTS OF BALB-3T3 CELLS .3. HYBRIDS BETWEEN TS2 AND OTHER MOUSE MUTANT-CELLS AFFECTED IN DNA-SYNTHESIS AND CORRECTION OF TS2 DEFECT BY HUMAN X-CHROMOSOME [J].
JHA, KK ;
SINISCALCO, M ;
OZER, HL .
SOMATIC CELL GENETICS, 1980, 6 (05) :603-614
[20]   A TRANSFORMATION-ASSOCIATED 130-KD CELL-SURFACE GLYCOPROTEIN IS GROWTH CONTROLLED IN NORMAL HUMAN-CELLS [J].
KLEIN, CE ;
OZER, HL ;
TRAGANOS, F ;
ATZPODIEN, J ;
OETTGEN, HF ;
OLD, LJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (05) :1684-1696