Increment of DNA topoisomerases in chemically and virally transformed cells

The activities of topoisomerases I and II were assayed in subcellular extracts obtained from nontumorigenic BALB/c 3T3 A31 and normal rat kidney (NRK) cell lines and from the same cells transformed by benzo[a]pyrene (BP-A31), Moloney (M-MSV-A31) and Kirsten (K-A31) sarcoma viruses, and simian virus...

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Publicado: 1988
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00144827_v175_n1_p206_Crespi
http://hdl.handle.net/20.500.12110/paper_00144827_v175_n1_p206_Crespi
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spelling paper:paper_00144827_v175_n1_p206_Crespi2023-06-08T14:37:14Z Increment of DNA topoisomerases in chemically and virally transformed cells benzo[a]pyrene isomerase radioisotope animal cell cell culture kidney mouse nonhuman rat sarcoma virus simian virus Animal Benzo(a)pyrene Cell Adhesion Cell Nucleus Cell Transformation, Neoplastic Cell Transformation, Viral DNA Topoisomerases, Type I Mice Novobiocin Rats Support, Non-U.S. Gov't The activities of topoisomerases I and II were assayed in subcellular extracts obtained from nontumorigenic BALB/c 3T3 A31 and normal rat kidney (NRK) cell lines and from the same cells transformed by benzo[a]pyrene (BP-A31), Moloney (M-MSV-A31) and Kirsten (K-A31) sarcoma viruses, and simian virus 40 (SV-NRK). The enzymatic activity of topoisomerase I was monitored by the relaxation of negatively supercoiled pBR322 DNA and by the formation of covalent complexes between 32P-labeled DNA and topoisomerase I. Topoisomerase II activity was determined by decatenation of kinetoplast DNA (k-DNA). It was found that nuclear and cytoplasmic type I topoisomerase specific activities were higher in every transformed cell line than in the normal counterparts. These differences cannot be attributed to an inhibitory factor present in A31 cells. When chromatin was treated at increasing ionic strengths, the 0.4 M NaCl extract showed the highest topoisomerase I specific activity. Moreover, in this fraction the transformed cells exhibited the most significant increment in the enzymatic activity as compared with nontransformed cultures. Spontaneously transformed A31 cells showed topoisomerase I activity similar to that of extracts of cells transformed by benzo[a]pyrene. Topoisomerase II specific activity was also increased in SV-NRK cells, as judged by the assay for decatenation of k-DNA to yield minicircle DNA. © 1988. 1988 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00144827_v175_n1_p206_Crespi http://hdl.handle.net/20.500.12110/paper_00144827_v175_n1_p206_Crespi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic benzo[a]pyrene
isomerase
radioisotope
animal cell
cell culture
kidney
mouse
nonhuman
rat
sarcoma virus
simian virus
Animal
Benzo(a)pyrene
Cell Adhesion
Cell Nucleus
Cell Transformation, Neoplastic
Cell Transformation, Viral
DNA Topoisomerases, Type I
Mice
Novobiocin
Rats
Support, Non-U.S. Gov't
spellingShingle benzo[a]pyrene
isomerase
radioisotope
animal cell
cell culture
kidney
mouse
nonhuman
rat
sarcoma virus
simian virus
Animal
Benzo(a)pyrene
Cell Adhesion
Cell Nucleus
Cell Transformation, Neoplastic
Cell Transformation, Viral
DNA Topoisomerases, Type I
Mice
Novobiocin
Rats
Support, Non-U.S. Gov't
Increment of DNA topoisomerases in chemically and virally transformed cells
topic_facet benzo[a]pyrene
isomerase
radioisotope
animal cell
cell culture
kidney
mouse
nonhuman
rat
sarcoma virus
simian virus
Animal
Benzo(a)pyrene
Cell Adhesion
Cell Nucleus
Cell Transformation, Neoplastic
Cell Transformation, Viral
DNA Topoisomerases, Type I
Mice
Novobiocin
Rats
Support, Non-U.S. Gov't
description The activities of topoisomerases I and II were assayed in subcellular extracts obtained from nontumorigenic BALB/c 3T3 A31 and normal rat kidney (NRK) cell lines and from the same cells transformed by benzo[a]pyrene (BP-A31), Moloney (M-MSV-A31) and Kirsten (K-A31) sarcoma viruses, and simian virus 40 (SV-NRK). The enzymatic activity of topoisomerase I was monitored by the relaxation of negatively supercoiled pBR322 DNA and by the formation of covalent complexes between 32P-labeled DNA and topoisomerase I. Topoisomerase II activity was determined by decatenation of kinetoplast DNA (k-DNA). It was found that nuclear and cytoplasmic type I topoisomerase specific activities were higher in every transformed cell line than in the normal counterparts. These differences cannot be attributed to an inhibitory factor present in A31 cells. When chromatin was treated at increasing ionic strengths, the 0.4 M NaCl extract showed the highest topoisomerase I specific activity. Moreover, in this fraction the transformed cells exhibited the most significant increment in the enzymatic activity as compared with nontransformed cultures. Spontaneously transformed A31 cells showed topoisomerase I activity similar to that of extracts of cells transformed by benzo[a]pyrene. Topoisomerase II specific activity was also increased in SV-NRK cells, as judged by the assay for decatenation of k-DNA to yield minicircle DNA. © 1988.
title Increment of DNA topoisomerases in chemically and virally transformed cells
title_short Increment of DNA topoisomerases in chemically and virally transformed cells
title_full Increment of DNA topoisomerases in chemically and virally transformed cells
title_fullStr Increment of DNA topoisomerases in chemically and virally transformed cells
title_full_unstemmed Increment of DNA topoisomerases in chemically and virally transformed cells
title_sort increment of dna topoisomerases in chemically and virally transformed cells
publishDate 1988
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00144827_v175_n1_p206_Crespi
http://hdl.handle.net/20.500.12110/paper_00144827_v175_n1_p206_Crespi
_version_ 1768544805031247872