Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Tumor Immunology: New Perspectives
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 41, 3133-3136, August 1, 1981]
© 1981 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gupta, P. K.
Right arrow Articles by Sirover, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gupta, P. K.
Right arrow Articles by Sirover, M. A.

Stimulation of the Nuclear Uracil DNA Glycosylase in Proliferating Human Fibroblasts1

Pawan K. Gupta and Michael A. Sirover

Fels Research Institute and the Department of Pharmacology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140

The cell cycle stimulation of individual species of the uracil DNA glycosylase was examined in WI-38 normal diploid fibroblasts. The nuclear uracil DNA glycosylase was induced as WI-38 cells traversed the cell cycle. In contrast, the specific activity of the mitochondrial glycosylase remained constant during cell proliferation. The two enzyme activities can be further distinguished by their elution patterns on DNA-cellulose, by differential cation sensitivity, and by kinetic differences. The singular stimulation of the nuclear glycosylase in the cell cycle is a further suggestion that normal human cells actively regulate excision repair pathways.

1 This study was supported by grant from the NIH (ES-01735), by a grant from the National Science Foundation (PCM-77-20183), by grants to this Institute from the NIH (CA 12227), and by a grant from the American Cancer Society (Grant IN-88J).

Received 1/23/81. Accepted 5/13/81.




This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
N. Scaramozzino, G. Sanz, J. M. Crance, M. Saparbaev, R. Drillien, J. Laval, B. Kavli, and D. Garin
Characterisation of the substrate specificity of homogeneous vaccinia virus uracil-DNA glycosylase
Nucleic Acids Res., August 15, 2003; 31(16): 4950 - 4957.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1981 by the American Association for Cancer Research.