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DNA Polymerases α and β Are Required for DNA Repair in an Efficient Nuclear Extract from Xenopus Oocytes
Xenopus oocytes and an oocyte nuclear extract efficiently repair the bulky DNA lesions cyclobutane pyrimidine dimers, (6-4) photoproducts, and N-acetoxy-2-aminofluorene (AAF) adducts by an excision repair mechanism. Nearly all (>95%) of the input damaged DNA was repaired within 5 h in both inject...
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Published in: | The Journal of biological chemistry 1996-06, Vol.271 (23), p.13816-13820 |
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container_end_page | 13820 |
container_issue | 23 |
container_start_page | 13816 |
container_title | The Journal of biological chemistry |
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creator | Oda, Naoko Saxena, Jitendra K. Jenkins, Timothy M. Prasad, Rajendra Wilson, Samuel H. Ackerman, Eric J. |
description | Xenopus oocytes and an oocyte nuclear extract efficiently repair the bulky DNA lesions cyclobutane pyrimidine dimers, (6-4) photoproducts, and N-acetoxy-2-aminofluorene (AAF) adducts by an excision repair mechanism. Nearly all (>95%) of the input damaged DNA was repaired within 5 h in both injected cells and extracts with no significant incorporation of label into control undamaged DNA. Remarkably, more than 1010 cyclobutane pyrimidine dimers or (6-4) photoproducts are repaired/nuclei. The extracts are free from nuclease activity, and repair is independent of exogenous light. Both the high efficiency and DNA polymerase requirements of this system appear to be different from extracts derived from human cells. We demonstrated a requirement for DNA polymerases α and β in repair of both photoproducts and AAF by inhibiting repair with several independent antibodies specific to either DNA polymerases α or β and then restoring repair by adding the appropriate purified polymerase. Repair is inhibited by aphidicolin at concentrations specific for blocking DNA polymerase α and dideoxynucleotide triphosphates at concentrations specific for inhibiting DNA polymerase β. |
doi_str_mv | 10.1074/jbc.271.23.13816 |
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Nearly all (>95%) of the input damaged DNA was repaired within 5 h in both injected cells and extracts with no significant incorporation of label into control undamaged DNA. Remarkably, more than 1010 cyclobutane pyrimidine dimers or (6-4) photoproducts are repaired/nuclei. The extracts are free from nuclease activity, and repair is independent of exogenous light. Both the high efficiency and DNA polymerase requirements of this system appear to be different from extracts derived from human cells. We demonstrated a requirement for DNA polymerases α and β in repair of both photoproducts and AAF by inhibiting repair with several independent antibodies specific to either DNA polymerases α or β and then restoring repair by adding the appropriate purified polymerase. Repair is inhibited by aphidicolin at concentrations specific for blocking DNA polymerase α and dideoxynucleotide triphosphates at concentrations specific for inhibiting DNA polymerase β.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.271.23.13816</identifier><identifier>PMID: 8662731</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antibodies - pharmacology ; Aphidicolin - pharmacology ; Cell Nucleus - metabolism ; DNA Polymerase I - antagonists & inhibitors ; DNA Polymerase I - metabolism ; DNA Polymerase II - antagonists & inhibitors ; DNA Polymerase II - metabolism ; DNA Repair - physiology ; Enzyme Inhibitors - pharmacology ; Female ; Freshwater ; Humans ; In Vitro Techniques ; Oocytes - metabolism ; Pyrimidine Dimers - metabolism ; Pyrimidine Dimers - radiation effects ; Ultraviolet Rays ; Xenopus</subject><ispartof>The Journal of biological chemistry, 1996-06, Vol.271 (23), p.13816-13820</ispartof><rights>1996 © 1996 ASBMB. 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Repair is inhibited by aphidicolin at concentrations specific for blocking DNA polymerase α and dideoxynucleotide triphosphates at concentrations specific for inhibiting DNA polymerase β.</description><subject>Animals</subject><subject>Antibodies - pharmacology</subject><subject>Aphidicolin - pharmacology</subject><subject>Cell Nucleus - metabolism</subject><subject>DNA Polymerase I - antagonists & inhibitors</subject><subject>DNA Polymerase I - metabolism</subject><subject>DNA Polymerase II - antagonists & inhibitors</subject><subject>DNA Polymerase II - metabolism</subject><subject>DNA Repair - physiology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Freshwater</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Oocytes - metabolism</subject><subject>Pyrimidine Dimers - metabolism</subject><subject>Pyrimidine Dimers - radiation effects</subject><subject>Ultraviolet Rays</subject><subject>Xenopus</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkUFr3DAQhUVJSbdp770UdMrNG41kraXelmTTBEJSQgu5CVkegxbb2kh2yP6s9ofkN0XbXXIrncsc5nsP5j1CvgCbA6vKs3Xt5ryCORdzEAoW78gMmBKFkPBwRGaMcSg0l-oD-ZjSmuUpNRyTY7VY8ErAjKwvbpf0R-i2PUabMNGX39QODX35Q5cR6T0-Tj5iQ9sQ6Q69x431kfohU3TVtt55HEZ6O7kObaSr5zFaN9I2hp4-4BA2U6J3wW1HTJ_I-9Z2CT8f9gn5dbn6eX5V3Nx9vz5f3hSuBDUWVjpseKWlrARCXTMrULVKobSlVKyWoK1CFJZX1sqGgWZWlaKtNa-h1JU4Iad7300MjxOm0fQ-Oew6O2CYkqkUiBK4_C8IcsG0KHUG2R50MaQUsTWb6HsbtwaY2fVgcg8m92C4MH97yJKvB--p7rF5ExyCz_dv-zvmJJ48RpN2SebXc9xuNE3w_zZ_BfjPl4A</recordid><startdate>19960607</startdate><enddate>19960607</enddate><creator>Oda, Naoko</creator><creator>Saxena, Jitendra K.</creator><creator>Jenkins, Timothy M.</creator><creator>Prasad, Rajendra</creator><creator>Wilson, Samuel H.</creator><creator>Ackerman, Eric J.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>19960607</creationdate><title>DNA Polymerases α and β Are Required for DNA Repair in an Efficient Nuclear Extract from Xenopus Oocytes</title><author>Oda, Naoko ; 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subjects | Animals Antibodies - pharmacology Aphidicolin - pharmacology Cell Nucleus - metabolism DNA Polymerase I - antagonists & inhibitors DNA Polymerase I - metabolism DNA Polymerase II - antagonists & inhibitors DNA Polymerase II - metabolism DNA Repair - physiology Enzyme Inhibitors - pharmacology Female Freshwater Humans In Vitro Techniques Oocytes - metabolism Pyrimidine Dimers - metabolism Pyrimidine Dimers - radiation effects Ultraviolet Rays Xenopus |
title | DNA Polymerases α and β Are Required for DNA Repair in an Efficient Nuclear Extract from Xenopus Oocytes |
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