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Hydrogen peroxide and sequence‐specific DNA damage in human cells
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Zeitschriftentitel: | FEBS Letters |
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Personen und Körperschaften: | , , , |
In: | FEBS Letters, 383, 1996, 3, S. 150-154 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Wiley
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Schlagwörter: |
author_facet |
Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul |
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author |
Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul |
spellingShingle |
Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul FEBS Letters Hydrogen peroxide and sequence‐specific DNA damage in human cells Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics |
author_sort |
burdon, r.h. |
spelling |
Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul 0014-5793 1873-3468 Wiley Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics http://dx.doi.org/10.1016/0014-5793(96)00230-x <jats:p>Exposure of HeLa cells in monolayer culture to increasing concentrations of exogenously added H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> causes damage to cellular DNA. When the DNA is subsequently isolated from the non‐apoptotic cells remaining in such cultures, evidence was obtained to suggest that the DNA damage elicited in intact cells was non‐random and that certain nucleotide sequences associated with, or related to, the genes for heat shock protein 60 and catalase were more susceptible to damage than others. In contrast, these particular sequences were not specifically susceptible to damage when naked human DNA was exposed directly to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vitro. On an overall comparative basis, sequences in the genes encoding catalase, α‐1 antitrypsin and β‐actin appear more vulnerable to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vivo, than sequences in <jats:italic>H‐ras</jats:italic> and the p53 gene which seem surprisingly resistant.</jats:p> Hydrogen peroxide and sequence‐specific DNA damage in human cells FEBS Letters |
doi_str_mv |
10.1016/0014-5793(96)00230-x |
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Biologie Chemie und Pharmazie Physik |
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Wiley, 1996 |
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Wiley, 1996 |
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1996 |
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Wiley |
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FEBS Letters |
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49 |
title |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_unstemmed |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_full |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_fullStr |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_full_unstemmed |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_short |
Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_sort |
hydrogen peroxide and sequence‐specific dna damage in human cells |
topic |
Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics |
url |
http://dx.doi.org/10.1016/0014-5793(96)00230-x |
publishDate |
1996 |
physical |
150-154 |
description |
<jats:p>Exposure of HeLa cells in monolayer culture to increasing concentrations of exogenously added H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> causes damage to cellular DNA. When the DNA is subsequently isolated from the non‐apoptotic cells remaining in such cultures, evidence was obtained to suggest that the DNA damage elicited in intact cells was non‐random and that certain nucleotide sequences associated with, or related to, the genes for heat shock protein 60 and catalase were more susceptible to damage than others. In contrast, these particular sequences were not specifically susceptible to damage when naked human DNA was exposed directly to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vitro. On an overall comparative basis, sequences in the genes encoding catalase, α‐1 antitrypsin and β‐actin appear more vulnerable to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vivo, than sequences in <jats:italic>H‐ras</jats:italic> and the p53 gene which seem surprisingly resistant.</jats:p> |
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author | Burdon, R.H., Gill, Vera, Boyd, Patricia A., Rahim, Raha Abdul |
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description | <jats:p>Exposure of HeLa cells in monolayer culture to increasing concentrations of exogenously added H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> causes damage to cellular DNA. When the DNA is subsequently isolated from the non‐apoptotic cells remaining in such cultures, evidence was obtained to suggest that the DNA damage elicited in intact cells was non‐random and that certain nucleotide sequences associated with, or related to, the genes for heat shock protein 60 and catalase were more susceptible to damage than others. In contrast, these particular sequences were not specifically susceptible to damage when naked human DNA was exposed directly to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vitro. On an overall comparative basis, sequences in the genes encoding catalase, α‐1 antitrypsin and β‐actin appear more vulnerable to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vivo, than sequences in <jats:italic>H‐ras</jats:italic> and the p53 gene which seem surprisingly resistant.</jats:p> |
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imprint | Wiley, 1996 |
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series | FEBS Letters |
source_id | 49 |
spelling | Burdon, R.H. Gill, Vera Boyd, Patricia A. Rahim, Raha Abdul 0014-5793 1873-3468 Wiley Cell Biology Genetics Molecular Biology Biochemistry Structural Biology Biophysics http://dx.doi.org/10.1016/0014-5793(96)00230-x <jats:p>Exposure of HeLa cells in monolayer culture to increasing concentrations of exogenously added H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> causes damage to cellular DNA. When the DNA is subsequently isolated from the non‐apoptotic cells remaining in such cultures, evidence was obtained to suggest that the DNA damage elicited in intact cells was non‐random and that certain nucleotide sequences associated with, or related to, the genes for heat shock protein 60 and catalase were more susceptible to damage than others. In contrast, these particular sequences were not specifically susceptible to damage when naked human DNA was exposed directly to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vitro. On an overall comparative basis, sequences in the genes encoding catalase, α‐1 antitrypsin and β‐actin appear more vulnerable to H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> in vivo, than sequences in <jats:italic>H‐ras</jats:italic> and the p53 gene which seem surprisingly resistant.</jats:p> Hydrogen peroxide and sequence‐specific DNA damage in human cells FEBS Letters |
spellingShingle | Burdon, R.H., Gill, Vera, Boyd, Patricia A., Rahim, Raha Abdul, FEBS Letters, Hydrogen peroxide and sequence‐specific DNA damage in human cells, Cell Biology, Genetics, Molecular Biology, Biochemistry, Structural Biology, Biophysics |
title | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_full | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_fullStr | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_full_unstemmed | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_short | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
title_sort | hydrogen peroxide and sequence‐specific dna damage in human cells |
title_unstemmed | Hydrogen peroxide and sequence‐specific DNA damage in human cells |
topic | Cell Biology, Genetics, Molecular Biology, Biochemistry, Structural Biology, Biophysics |
url | http://dx.doi.org/10.1016/0014-5793(96)00230-x |