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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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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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 |