Comparative analyses of the two proliferating cell nuclear antigens from the hyperthermophilic archaeon, Thermococcus kodakarensis
The DNA sliding clamp is a multifunctional protein involved in cellular DNA transactions. In Archaea and Eukaryota, proliferating cell nuclear antigen (PCNA) is the sliding clamp. The ring‐shaped PCNA encircles double‐stranded DNA within its central hole and tethers other proteins on DNA. The majori...
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Veröffentlicht in: | Genes to cells : devoted to molecular & cellular mechanisms 2012-11, Vol.17 (11), p.923-937 |
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creator | Kuba, Yumani Ishino, Sonoko Yamagami, Takeshi Tokuhara, Masahiro Kanai, Tamotsu Fujikane, Ryosuke Daiyasu, Hiromi Atomi, Haruyuki Ishino, Yoshizumi |
description | The DNA sliding clamp is a multifunctional protein involved in cellular DNA transactions. In Archaea and Eukaryota, proliferating cell nuclear antigen (PCNA) is the sliding clamp. The ring‐shaped PCNA encircles double‐stranded DNA within its central hole and tethers other proteins on DNA. The majority of Crenarchaeota, a subdomain of Archaea, have multiple PCNA homologues, and they are capable of forming heterotrimeric rings for their functions. In contrast, most organisms in Euryarchaeota, the other major subdomain, have a single PCNA forming a homotrimeric ring structure. Among the Euryarchaeota whose genome is sequenced, Thermococcus kodakarensis is the only species with two genes encoding PCNA homologues on its genome. We cloned the two genes from the T. kodakarensis genome, and the gene products, PCNA1 and PCNA2, were characterized. PCNA1 stimulated the DNA synthesis reactions of the two DNA polymerases, PolB and PolD, from T. kodakarensis in vitro. PCNA2, however, only had an effect on PolB. We were able to disrupt the gene for PCNA2, whereas gene disruption for PCNA1 was not possible, suggesting that PCNA1 is essential for DNA replication. The sensitivities of the Δpcna2 mutant strain to ultraviolet irradiation (UV), methyl methanesulfonate (MMS) and mitomycin C (MMC) were indistinguishable from those of the wild‐type strain. |
doi_str_mv | 10.1111/gtc.12007 |
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In Archaea and Eukaryota, proliferating cell nuclear antigen (PCNA) is the sliding clamp. The ring‐shaped PCNA encircles double‐stranded DNA within its central hole and tethers other proteins on DNA. The majority of Crenarchaeota, a subdomain of Archaea, have multiple PCNA homologues, and they are capable of forming heterotrimeric rings for their functions. In contrast, most organisms in Euryarchaeota, the other major subdomain, have a single PCNA forming a homotrimeric ring structure. Among the Euryarchaeota whose genome is sequenced, Thermococcus kodakarensis is the only species with two genes encoding PCNA homologues on its genome. We cloned the two genes from the T. kodakarensis genome, and the gene products, PCNA1 and PCNA2, were characterized. PCNA1 stimulated the DNA synthesis reactions of the two DNA polymerases, PolB and PolD, from T. kodakarensis in vitro. PCNA2, however, only had an effect on PolB. We were able to disrupt the gene for PCNA2, whereas gene disruption for PCNA1 was not possible, suggesting that PCNA1 is essential for DNA replication. The sensitivities of the Δpcna2 mutant strain to ultraviolet irradiation (UV), methyl methanesulfonate (MMS) and mitomycin C (MMC) were indistinguishable from those of the wild‐type strain.</description><identifier>ISSN: 1356-9597</identifier><identifier>EISSN: 1365-2443</identifier><identifier>DOI: 10.1111/gtc.12007</identifier><identifier>PMID: 23078585</identifier><language>eng</language><publisher>England</publisher><subject><![CDATA[Adenosine Triphosphatases - chemistry ; Adenosine Triphosphatases - isolation & purification ; Adenosine Triphosphatases - metabolism ; Archaea ; Archaeal Proteins - chemistry ; Archaeal Proteins - genetics ; Archaeal Proteins - isolation & purification ; Archaeal Proteins - metabolism ; Crenarchaeota ; DNA Damage ; DNA Polymerase beta - chemistry ; DNA Polymerase III - chemistry ; DNA Repair ; DNA Replication ; DNA, Archaeal - chemistry ; DNA, Archaeal - metabolism ; Euryarchaeota ; Gene Knockout Techniques ; Proliferating Cell Nuclear Antigen - chemistry ; Proliferating Cell Nuclear Antigen - genetics ; Proliferating Cell Nuclear Antigen - isolation & purification ; Proliferating Cell Nuclear Antigen - metabolism ; Protein Binding ; Protein Subunits - chemistry ; Protein Subunits - isolation & purification ; Protein Subunits - metabolism ; Replication Protein C - chemistry ; Replication Protein C - isolation & purification ; Replication Protein C - metabolism ; Thermococcus ; Thermococcus - genetics ; Thermococcus - growth & development ; Thermococcus - metabolism]]></subject><ispartof>Genes to cells : devoted to molecular & cellular mechanisms, 2012-11, Vol.17 (11), p.923-937</ispartof><rights>2012 The Authors Genes to Cells © 2012 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd</rights><rights>2012 The Authors Genes to Cells © 2012 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3937-39e20fb80c7b8b9bf9799d8342d940dd68faf73a8299804c4eeefd6e8c3a48883</citedby><cites>FETCH-LOGICAL-c3937-39e20fb80c7b8b9bf9799d8342d940dd68faf73a8299804c4eeefd6e8c3a48883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgtc.12007$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgtc.12007$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23078585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuba, Yumani</creatorcontrib><creatorcontrib>Ishino, Sonoko</creatorcontrib><creatorcontrib>Yamagami, Takeshi</creatorcontrib><creatorcontrib>Tokuhara, Masahiro</creatorcontrib><creatorcontrib>Kanai, Tamotsu</creatorcontrib><creatorcontrib>Fujikane, Ryosuke</creatorcontrib><creatorcontrib>Daiyasu, Hiromi</creatorcontrib><creatorcontrib>Atomi, Haruyuki</creatorcontrib><creatorcontrib>Ishino, Yoshizumi</creatorcontrib><title>Comparative analyses of the two proliferating cell nuclear antigens from the hyperthermophilic archaeon, Thermococcus kodakarensis</title><title>Genes to cells : devoted to molecular & cellular mechanisms</title><addtitle>Genes Cells</addtitle><description>The DNA sliding clamp is a multifunctional protein involved in cellular DNA transactions. In Archaea and Eukaryota, proliferating cell nuclear antigen (PCNA) is the sliding clamp. The ring‐shaped PCNA encircles double‐stranded DNA within its central hole and tethers other proteins on DNA. The majority of Crenarchaeota, a subdomain of Archaea, have multiple PCNA homologues, and they are capable of forming heterotrimeric rings for their functions. In contrast, most organisms in Euryarchaeota, the other major subdomain, have a single PCNA forming a homotrimeric ring structure. Among the Euryarchaeota whose genome is sequenced, Thermococcus kodakarensis is the only species with two genes encoding PCNA homologues on its genome. We cloned the two genes from the T. kodakarensis genome, and the gene products, PCNA1 and PCNA2, were characterized. PCNA1 stimulated the DNA synthesis reactions of the two DNA polymerases, PolB and PolD, from T. kodakarensis in vitro. PCNA2, however, only had an effect on PolB. We were able to disrupt the gene for PCNA2, whereas gene disruption for PCNA1 was not possible, suggesting that PCNA1 is essential for DNA replication. The sensitivities of the Δpcna2 mutant strain to ultraviolet irradiation (UV), methyl methanesulfonate (MMS) and mitomycin C (MMC) were indistinguishable from those of the wild‐type strain.</description><subject>Adenosine Triphosphatases - chemistry</subject><subject>Adenosine Triphosphatases - isolation & purification</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Archaea</subject><subject>Archaeal Proteins - chemistry</subject><subject>Archaeal Proteins - genetics</subject><subject>Archaeal Proteins - isolation & purification</subject><subject>Archaeal Proteins - metabolism</subject><subject>Crenarchaeota</subject><subject>DNA Damage</subject><subject>DNA Polymerase beta - chemistry</subject><subject>DNA Polymerase III - chemistry</subject><subject>DNA Repair</subject><subject>DNA Replication</subject><subject>DNA, Archaeal - chemistry</subject><subject>DNA, Archaeal - metabolism</subject><subject>Euryarchaeota</subject><subject>Gene Knockout Techniques</subject><subject>Proliferating Cell Nuclear Antigen - chemistry</subject><subject>Proliferating Cell Nuclear Antigen - genetics</subject><subject>Proliferating Cell Nuclear Antigen - isolation & purification</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Protein Binding</subject><subject>Protein Subunits - chemistry</subject><subject>Protein Subunits - isolation & purification</subject><subject>Protein Subunits - metabolism</subject><subject>Replication Protein C - chemistry</subject><subject>Replication Protein C - isolation & purification</subject><subject>Replication Protein C - metabolism</subject><subject>Thermococcus</subject><subject>Thermococcus - genetics</subject><subject>Thermococcus - growth & development</subject><subject>Thermococcus - metabolism</subject><issn>1356-9597</issn><issn>1365-2443</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0U1LxDAQBuAgit8H_4DkqGA1adpNcpTFLxC8rOeSppPduG1Tk1bZq7_cdHf1JphLhuGZF4ZB6IySaxrfzbzX1zQlhO-gQ8omeZJmGdsd63ySyFzyA3QUwhshlKUk30cHKSNc5CI_RF9T13TKq95-AFatqlcBAnYG9wvA_afDnXe1NTCKdo411DVuB12D8pH3dg5twMa7Zj2wWHXgY-Eb1y1sbTVWXi8UuPYKz9Zt7bQeAl66Si2Vj8M2nKA9o-oAp9v_GL3e382mj8nzy8PT9PY50UwynjAJKTGlIJqXopSlkVzKSrAsrWRGqmoijDKcKZFKKUimMwAw1QSEZioTQrBjdLHJjSu9DxD6orFhXEi14IZQUMqp4JwI9g9K8zwdeaSXG6q9C8GDKTpvG-VXBSWjo0W8TrG-TrTn29ihbKD6lT_niOBmAz5tDau_k4qH2XQT-Q0wM5wE</recordid><startdate>201211</startdate><enddate>201211</enddate><creator>Kuba, Yumani</creator><creator>Ishino, Sonoko</creator><creator>Yamagami, Takeshi</creator><creator>Tokuhara, Masahiro</creator><creator>Kanai, Tamotsu</creator><creator>Fujikane, Ryosuke</creator><creator>Daiyasu, Hiromi</creator><creator>Atomi, Haruyuki</creator><creator>Ishino, Yoshizumi</creator><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201211</creationdate><title>Comparative analyses of the two proliferating cell nuclear antigens from the hyperthermophilic archaeon, Thermococcus kodakarensis</title><author>Kuba, Yumani ; Ishino, Sonoko ; Yamagami, Takeshi ; Tokuhara, Masahiro ; Kanai, Tamotsu ; Fujikane, Ryosuke ; Daiyasu, Hiromi ; Atomi, Haruyuki ; Ishino, Yoshizumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3937-39e20fb80c7b8b9bf9799d8342d940dd68faf73a8299804c4eeefd6e8c3a48883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenosine Triphosphatases - chemistry</topic><topic>Adenosine Triphosphatases - isolation & purification</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Archaea</topic><topic>Archaeal Proteins - chemistry</topic><topic>Archaeal Proteins - genetics</topic><topic>Archaeal Proteins - isolation & purification</topic><topic>Archaeal Proteins - metabolism</topic><topic>Crenarchaeota</topic><topic>DNA Damage</topic><topic>DNA Polymerase beta - chemistry</topic><topic>DNA Polymerase III - chemistry</topic><topic>DNA Repair</topic><topic>DNA Replication</topic><topic>DNA, Archaeal - chemistry</topic><topic>DNA, Archaeal - metabolism</topic><topic>Euryarchaeota</topic><topic>Gene Knockout Techniques</topic><topic>Proliferating Cell Nuclear Antigen - chemistry</topic><topic>Proliferating Cell Nuclear Antigen - genetics</topic><topic>Proliferating Cell Nuclear Antigen - isolation & purification</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Protein Binding</topic><topic>Protein Subunits - chemistry</topic><topic>Protein Subunits - isolation & purification</topic><topic>Protein Subunits - metabolism</topic><topic>Replication Protein C - chemistry</topic><topic>Replication Protein C - isolation & purification</topic><topic>Replication Protein C - metabolism</topic><topic>Thermococcus</topic><topic>Thermococcus - genetics</topic><topic>Thermococcus - growth & development</topic><topic>Thermococcus - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuba, Yumani</creatorcontrib><creatorcontrib>Ishino, Sonoko</creatorcontrib><creatorcontrib>Yamagami, Takeshi</creatorcontrib><creatorcontrib>Tokuhara, Masahiro</creatorcontrib><creatorcontrib>Kanai, Tamotsu</creatorcontrib><creatorcontrib>Fujikane, Ryosuke</creatorcontrib><creatorcontrib>Daiyasu, Hiromi</creatorcontrib><creatorcontrib>Atomi, Haruyuki</creatorcontrib><creatorcontrib>Ishino, Yoshizumi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuba, Yumani</au><au>Ishino, Sonoko</au><au>Yamagami, Takeshi</au><au>Tokuhara, Masahiro</au><au>Kanai, Tamotsu</au><au>Fujikane, Ryosuke</au><au>Daiyasu, Hiromi</au><au>Atomi, Haruyuki</au><au>Ishino, Yoshizumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative analyses of the two proliferating cell nuclear antigens from the hyperthermophilic archaeon, Thermococcus kodakarensis</atitle><jtitle>Genes to cells : devoted to molecular & cellular mechanisms</jtitle><addtitle>Genes Cells</addtitle><date>2012-11</date><risdate>2012</risdate><volume>17</volume><issue>11</issue><spage>923</spage><epage>937</epage><pages>923-937</pages><issn>1356-9597</issn><eissn>1365-2443</eissn><abstract>The DNA sliding clamp is a multifunctional protein involved in cellular DNA transactions. In Archaea and Eukaryota, proliferating cell nuclear antigen (PCNA) is the sliding clamp. The ring‐shaped PCNA encircles double‐stranded DNA within its central hole and tethers other proteins on DNA. The majority of Crenarchaeota, a subdomain of Archaea, have multiple PCNA homologues, and they are capable of forming heterotrimeric rings for their functions. In contrast, most organisms in Euryarchaeota, the other major subdomain, have a single PCNA forming a homotrimeric ring structure. Among the Euryarchaeota whose genome is sequenced, Thermococcus kodakarensis is the only species with two genes encoding PCNA homologues on its genome. We cloned the two genes from the T. kodakarensis genome, and the gene products, PCNA1 and PCNA2, were characterized. PCNA1 stimulated the DNA synthesis reactions of the two DNA polymerases, PolB and PolD, from T. kodakarensis in vitro. PCNA2, however, only had an effect on PolB. We were able to disrupt the gene for PCNA2, whereas gene disruption for PCNA1 was not possible, suggesting that PCNA1 is essential for DNA replication. The sensitivities of the Δpcna2 mutant strain to ultraviolet irradiation (UV), methyl methanesulfonate (MMS) and mitomycin C (MMC) were indistinguishable from those of the wild‐type strain.</abstract><cop>England</cop><pmid>23078585</pmid><doi>10.1111/gtc.12007</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphatases - chemistry Adenosine Triphosphatases - isolation & purification Adenosine Triphosphatases - metabolism Archaea Archaeal Proteins - chemistry Archaeal Proteins - genetics Archaeal Proteins - isolation & purification Archaeal Proteins - metabolism Crenarchaeota DNA Damage DNA Polymerase beta - chemistry DNA Polymerase III - chemistry DNA Repair DNA Replication DNA, Archaeal - chemistry DNA, Archaeal - metabolism Euryarchaeota Gene Knockout Techniques Proliferating Cell Nuclear Antigen - chemistry Proliferating Cell Nuclear Antigen - genetics Proliferating Cell Nuclear Antigen - isolation & purification Proliferating Cell Nuclear Antigen - metabolism Protein Binding Protein Subunits - chemistry Protein Subunits - isolation & purification Protein Subunits - metabolism Replication Protein C - chemistry Replication Protein C - isolation & purification Replication Protein C - metabolism Thermococcus Thermococcus - genetics Thermococcus - growth & development Thermococcus - metabolism |
title | Comparative analyses of the two proliferating cell nuclear antigens from the hyperthermophilic archaeon, Thermococcus kodakarensis |
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