The Hsk1(Cdc7) replication kinase regulates origin efficiency
Origins of DNA replication are generally inefficient, with most firing in fewer than half of cell cycles. However, neither the mechanism nor the importance of the regulation of origin efficiency is clear. In fission yeast, origin firing is stochastic, leading us to hypothesize that origin inefficien...
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Veröffentlicht in: | Molecular biology of the cell 2008-12, Vol.19 (12), p.5550-5558 |
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creator | Patel, Prasanta K Kommajosyula, Naveen Rosebrock, Adam Bensimon, Aaron Leatherwood, Janet Bechhoefer, John Rhind, Nicholas |
description | Origins of DNA replication are generally inefficient, with most firing in fewer than half of cell cycles. However, neither the mechanism nor the importance of the regulation of origin efficiency is clear. In fission yeast, origin firing is stochastic, leading us to hypothesize that origin inefficiency and stochasticity are the result of a diffusible, rate-limiting activator. We show that the Hsk1-Dfp1 replication kinase (the fission yeast Cdc7-Dbf4 homologue) plays such a role. Increasing or decreasing Hsk1-Dfp1 levels correspondingly increases or decreases origin efficiency. Furthermore, tethering Hsk1-Dfp1 near an origin increases the efficiency of that origin, suggesting that the effective local concentration of Hsk1-Dfp1 regulates origin firing. Using photobleaching, we show that Hsk1-Dfp1 is freely diffusible in the nucleus. These results support a model in which the accessibility of replication origins to Hsk1-Dfp1 regulates origin efficiency and provides a potential mechanistic link between chromatin structure and replication timing. By manipulating Hsk1-Dfp1 levels, we show that increasing or decreasing origin firing rates leads to an increase in genomic instability, demonstrating the biological importance of appropriate origin efficiency. |
doi_str_mv | 10.1091/mbc.E08-06-0645 |
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However, neither the mechanism nor the importance of the regulation of origin efficiency is clear. In fission yeast, origin firing is stochastic, leading us to hypothesize that origin inefficiency and stochasticity are the result of a diffusible, rate-limiting activator. We show that the Hsk1-Dfp1 replication kinase (the fission yeast Cdc7-Dbf4 homologue) plays such a role. Increasing or decreasing Hsk1-Dfp1 levels correspondingly increases or decreases origin efficiency. Furthermore, tethering Hsk1-Dfp1 near an origin increases the efficiency of that origin, suggesting that the effective local concentration of Hsk1-Dfp1 regulates origin firing. Using photobleaching, we show that Hsk1-Dfp1 is freely diffusible in the nucleus. These results support a model in which the accessibility of replication origins to Hsk1-Dfp1 regulates origin efficiency and provides a potential mechanistic link between chromatin structure and replication timing. 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However, neither the mechanism nor the importance of the regulation of origin efficiency is clear. In fission yeast, origin firing is stochastic, leading us to hypothesize that origin inefficiency and stochasticity are the result of a diffusible, rate-limiting activator. We show that the Hsk1-Dfp1 replication kinase (the fission yeast Cdc7-Dbf4 homologue) plays such a role. Increasing or decreasing Hsk1-Dfp1 levels correspondingly increases or decreases origin efficiency. Furthermore, tethering Hsk1-Dfp1 near an origin increases the efficiency of that origin, suggesting that the effective local concentration of Hsk1-Dfp1 regulates origin firing. Using photobleaching, we show that Hsk1-Dfp1 is freely diffusible in the nucleus. These results support a model in which the accessibility of replication origins to Hsk1-Dfp1 regulates origin efficiency and provides a potential mechanistic link between chromatin structure and replication timing. By manipulating Hsk1-Dfp1 levels, we show that increasing or decreasing origin firing rates leads to an increase in genomic instability, demonstrating the biological importance of appropriate origin efficiency.</description><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Nucleus - metabolism</subject><subject>Chromosomal Instability</subject><subject>DNA Replication</subject><subject>Fluorescence Recovery After Photobleaching</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Plasmids - genetics</subject><subject>Plasmids - metabolism</subject><subject>Protein Kinases - genetics</subject><subject>Protein Kinases - metabolism</subject><subject>Protein Serine-Threonine Kinases - genetics</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Replication Origin</subject><subject>Schizosaccharomyces - cytology</subject><subject>Schizosaccharomyces - physiology</subject><subject>Schizosaccharomyces pombe Proteins - genetics</subject><subject>Schizosaccharomyces pombe Proteins - metabolism</subject><issn>1059-1524</issn><issn>1939-4586</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1LAzEQhoMotlbP3mRPoodtk2w-NgcFKdUKBS_1HJJ00sZud-tmV-i_d0uLHzAww8w77wwPQtcEDwlWZLSxbjjBeYpFF4yfoD5RmUoZz8VpV2OuUsIp66GLGD8wJowJeY56JJdKCUL76GG-gmQa1-RuvHDyPqlhWwRnmlCVyTqUJkLXWraFaSAmVR2WoUzA--AClG53ic68KSJcHfMAvT9P5uNpOnt7eR0_zVLHM96kTFoOsrvpKTBipDDe5pLm1hsJJANlsGWeKbcgFiymmFpJCAhOZM4AXDZAjwffbWs3sHBQNrUp9LYOG1PvdGWC_j8pw0ovqy9NuaKCic7g9mhQV58txEZvQnRQFKaEqo1aqJxlVNBOODoIXV3FWIP_OUKw3iPXHXINONdY6D3ybuPm72-_-iPj7Bt-g34N</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Patel, Prasanta K</creator><creator>Kommajosyula, Naveen</creator><creator>Rosebrock, Adam</creator><creator>Bensimon, Aaron</creator><creator>Leatherwood, Janet</creator><creator>Bechhoefer, John</creator><creator>Rhind, Nicholas</creator><general>The American Society for Cell Biology</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>200812</creationdate><title>The Hsk1(Cdc7) replication kinase regulates origin efficiency</title><author>Patel, Prasanta K ; 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However, neither the mechanism nor the importance of the regulation of origin efficiency is clear. In fission yeast, origin firing is stochastic, leading us to hypothesize that origin inefficiency and stochasticity are the result of a diffusible, rate-limiting activator. We show that the Hsk1-Dfp1 replication kinase (the fission yeast Cdc7-Dbf4 homologue) plays such a role. Increasing or decreasing Hsk1-Dfp1 levels correspondingly increases or decreases origin efficiency. Furthermore, tethering Hsk1-Dfp1 near an origin increases the efficiency of that origin, suggesting that the effective local concentration of Hsk1-Dfp1 regulates origin firing. Using photobleaching, we show that Hsk1-Dfp1 is freely diffusible in the nucleus. These results support a model in which the accessibility of replication origins to Hsk1-Dfp1 regulates origin efficiency and provides a potential mechanistic link between chromatin structure and replication timing. 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subjects | Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cell Nucleus - metabolism Chromosomal Instability DNA Replication Fluorescence Recovery After Photobleaching Gene Expression Regulation, Fungal Plasmids - genetics Plasmids - metabolism Protein Kinases - genetics Protein Kinases - metabolism Protein Serine-Threonine Kinases - genetics Protein Serine-Threonine Kinases - metabolism Replication Origin Schizosaccharomyces - cytology Schizosaccharomyces - physiology Schizosaccharomyces pombe Proteins - genetics Schizosaccharomyces pombe Proteins - metabolism |
title | The Hsk1(Cdc7) replication kinase regulates origin efficiency |
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