Relationship of DNA degradation by Saccharomyces cerevisiae Exonuclease 1 and its stimulation by RPA and Mre11-Rad50-Xrs2 to DNA end resection
Significance The repair of double-strand DNA breaks by homologous recombination is initiated by the nucleolytic resection of the 5′-terminated strand at the DNA break. Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2013-04, Vol.110 (18), p.E1661-E1668 |
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creator | Cannavo, Elda Cejka, Petr Kowalczykowski, Stephen C |
description | Significance The repair of double-strand DNA breaks by homologous recombination is initiated by the nucleolytic resection of the 5′-terminated strand at the DNA break. Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo1. Here we investigated the relationship between the three nucleolytic complexes in vitro. With a focus on Exo1, we show that it is stimulated by the single-strand DNA-binding protein, RPA, and also by the Mre11-Rad50-Xrs2 complex. Furthermore, our analysis provides biochemical evidence for the view that Exo1 and Dna2-Sgs1-Top3-Rmi1 function downstream of Mre11-Rad50-Xrs2 as independent and mutually exclusive DNA end-processing pathways. |
doi_str_mv | 10.1073/pnas.1305166110 |
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Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo1. Here we investigated the relationship between the three nucleolytic complexes in vitro. With a focus on Exo1, we show that it is stimulated by the single-strand DNA-binding protein, RPA, and also by the Mre11-Rad50-Xrs2 complex. Furthermore, our analysis provides biochemical evidence for the view that Exo1 and Dna2-Sgs1-Top3-Rmi1 function downstream of Mre11-Rad50-Xrs2 as independent and mutually exclusive DNA end-processing pathways.</description><subject>Biological Sciences</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Breaks, Single-Stranded</subject><subject>DNA, Fungal - metabolism</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Endodeoxyribonucleases - metabolism</subject><subject>Exodeoxyribonucleases - metabolism</subject><subject>Mutation</subject><subject>PNAS Plus</subject><subject>Proteins</subject><subject>Replication Protein A - metabolism</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Yeast</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtv1DAUhSMEokNhzQ4ssWGT9t7EcZwN0qhMAak8NKUSO8txbmZcJfHUTqrOn-A3k8wMw2Nlyec75_r6RNFLhDOEPD3fdDqcYQoZCoEIj6IZQoGx4AU8jmYASR5LnvCT6FkItwBQZBKeRidJmslCZnIW_VxSo3vrurC2G-Zq9v7LnFW08rraXbNyy661MWvtXbs1FJghT_c2WE1s8eC6wTSkAzFkuquY7QMLvW2H5uhefpvvpM-eEOOlrjKIf_iQsN7thtGoeQpkJsPz6Emtm0AvDudpdHO5-H7xMb76-uHTxfwqNjyHPk7BFAZEbZKES6nrtK4IM0ilzGtTSkA0SYZG5CgIihLyXJqqxJqj1KUUMj2N3u1zN0PZUmWo671u1MbbVvutctqqf5XOrtXK3atU8CzjyRjw9hDg3d1AoVetDYaaRnfkhqAw5ePQgiMf0Tf_obdu8N243kRJFBnHKfB8TxnvQvBUHx-DoKau1dS1-tP16Hj19w5H_ne5I8AOwOQ8xk15Ui2mlBF5vUdq7ZReeRvUzXUCKAAwzcX4pb8A58u4oQ</recordid><startdate>20130430</startdate><enddate>20130430</enddate><creator>Cannavo, Elda</creator><creator>Cejka, Petr</creator><creator>Kowalczykowski, Stephen C</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130430</creationdate><title>Relationship of DNA degradation by Saccharomyces cerevisiae Exonuclease 1 and its stimulation by RPA and Mre11-Rad50-Xrs2 to DNA end resection</title><author>Cannavo, Elda ; 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Genetic work in Saccharomyces cerevisiae identified three DNA end resection pathways: Mre11-Rad50-Xrs2, Dna2-Sgs1-Top3-Rmi1, and Exo1. Here we investigated the relationship between the three nucleolytic complexes in vitro. With a focus on Exo1, we show that it is stimulated by the single-strand DNA-binding protein, RPA, and also by the Mre11-Rad50-Xrs2 complex. Furthermore, our analysis provides biochemical evidence for the view that Exo1 and Dna2-Sgs1-Top3-Rmi1 function downstream of Mre11-Rad50-Xrs2 as independent and mutually exclusive DNA end-processing pathways.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>23589858</pmid><doi>10.1073/pnas.1305166110</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biological Sciences Deoxyribonucleic acid DNA DNA Breaks, Single-Stranded DNA, Fungal - metabolism DNA-Binding Proteins - metabolism Endodeoxyribonucleases - metabolism Exodeoxyribonucleases - metabolism Mutation PNAS Plus Proteins Replication Protein A - metabolism Saccharomyces cerevisiae - enzymology Saccharomyces cerevisiae Proteins - metabolism Yeast |
title | Relationship of DNA degradation by Saccharomyces cerevisiae Exonuclease 1 and its stimulation by RPA and Mre11-Rad50-Xrs2 to DNA end resection |
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