HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail

The high mobility group box (HMGB) 1 protein is a very abundant and conserved protein that is implicated in many key cellular events but its functions within the nucleus remain elusive. The role of this protein in replication of closed circular DNA containing a eukaryotic origin of replication has b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The international journal of biochemistry & cell biology 2008, Vol.40 (8), p.1536-1542
Hauptverfasser: Topalova, Dessislava, Ugrinova, Iva, Pashev, Iliya G., Pasheva, Evdokia A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1542
container_issue 8
container_start_page 1536
container_title The international journal of biochemistry & cell biology
container_volume 40
creator Topalova, Dessislava
Ugrinova, Iva
Pashev, Iliya G.
Pasheva, Evdokia A.
description The high mobility group box (HMGB) 1 protein is a very abundant and conserved protein that is implicated in many key cellular events but its functions within the nucleus remain elusive. The role of this protein in replication of closed circular DNA containing a eukaryotic origin of replication has been studied in vitro by using native and recombinant HMGB1 as well as various modified HMGB1 preparations such as truncated protein, lacking its C-terminal tail, in vivo acetylated protein, and recombinant HMGB1 phosphorylated in vitro by protein kinase C (PKC). Native HMGB1 extracted from tumour cells inhibits replication and this effect is reduced upon acetylation and completely abolished upon removal of the acidic C-terminal tail. Recombinant HMGB1, however, fails to inhibit replication but it acquires such a property following in vitro phosphorylation by PKC.
doi_str_mv 10.1016/j.biocel.2007.11.014
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69174752</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1357272507003986</els_id><sourcerecordid>69174752</sourcerecordid><originalsourceid>FETCH-LOGICAL-c360t-adf71ac6ee02a126fd970a6c6c2e5858b18a64c728c034415f974c87220adfe33</originalsourceid><addsrcrecordid>eNp9kE9P3DAQxS1ExZ-l3wAhn7gl9TiJ7eWARCmFSrS90GstrzMRs8rGW9uLxLevV1mpt55mNPPejN6PsUsQNQhQn9b1ioLHsZZC6BqgFtAesTMw2lSd0d1x6ZtOV1LL7pSdp7QWQkAnmxN2CgaWoECesd9P3x8_A9_GkJEmTtMrrSgn_uXHHY-4Hcm7TGG_4G-UY7jhZR5G5GHg-RW585jfx1njpv4wo548z47GC_ZhcGPCj4e6YL--PrzcP1XPPx-_3d89V75RIleuHzQ4rxCFdCDV0C-1cMorL7EznVmBcar1WhovmraFbljq1hstpShWbJoFu57vliB_dpiy3VAqcEY3Ydglq5agW13CL1g7C30MKUUc7DbSxsV3C8Luudq1nbnaPVcLYAvXYrs63N-tNtj_Mx1AFsHtLMCS8o0w2uQJJ489RfTZ9oH-_-EvdaGJ_Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69174752</pqid></control><display><type>article</type><title>HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Topalova, Dessislava ; Ugrinova, Iva ; Pashev, Iliya G. ; Pasheva, Evdokia A.</creator><creatorcontrib>Topalova, Dessislava ; Ugrinova, Iva ; Pashev, Iliya G. ; Pasheva, Evdokia A.</creatorcontrib><description>The high mobility group box (HMGB) 1 protein is a very abundant and conserved protein that is implicated in many key cellular events but its functions within the nucleus remain elusive. The role of this protein in replication of closed circular DNA containing a eukaryotic origin of replication has been studied in vitro by using native and recombinant HMGB1 as well as various modified HMGB1 preparations such as truncated protein, lacking its C-terminal tail, in vivo acetylated protein, and recombinant HMGB1 phosphorylated in vitro by protein kinase C (PKC). Native HMGB1 extracted from tumour cells inhibits replication and this effect is reduced upon acetylation and completely abolished upon removal of the acidic C-terminal tail. Recombinant HMGB1, however, fails to inhibit replication but it acquires such a property following in vitro phosphorylation by PKC.</description><identifier>ISSN: 1357-2725</identifier><identifier>EISSN: 1878-5875</identifier><identifier>DOI: 10.1016/j.biocel.2007.11.014</identifier><identifier>PMID: 18191612</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Acetylation ; Acidic tail ; Animals ; Aphidicolin - pharmacology ; DNA replication ; DNA Replication - drug effects ; DNA, Circular - metabolism ; High Mobility Group Proteins - pharmacology ; HMGB1 Protein ; Humans ; Phosphorylation ; Protein Kinase C - metabolism ; Rats ; Recombinant Proteins - pharmacology ; Repressor Proteins - pharmacology ; Tumor Cells, Cultured</subject><ispartof>The international journal of biochemistry &amp; cell biology, 2008, Vol.40 (8), p.1536-1542</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-adf71ac6ee02a126fd970a6c6c2e5858b18a64c728c034415f974c87220adfe33</citedby><cites>FETCH-LOGICAL-c360t-adf71ac6ee02a126fd970a6c6c2e5858b18a64c728c034415f974c87220adfe33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biocel.2007.11.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,4010,27904,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18191612$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Topalova, Dessislava</creatorcontrib><creatorcontrib>Ugrinova, Iva</creatorcontrib><creatorcontrib>Pashev, Iliya G.</creatorcontrib><creatorcontrib>Pasheva, Evdokia A.</creatorcontrib><title>HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail</title><title>The international journal of biochemistry &amp; cell biology</title><addtitle>Int J Biochem Cell Biol</addtitle><description>The high mobility group box (HMGB) 1 protein is a very abundant and conserved protein that is implicated in many key cellular events but its functions within the nucleus remain elusive. The role of this protein in replication of closed circular DNA containing a eukaryotic origin of replication has been studied in vitro by using native and recombinant HMGB1 as well as various modified HMGB1 preparations such as truncated protein, lacking its C-terminal tail, in vivo acetylated protein, and recombinant HMGB1 phosphorylated in vitro by protein kinase C (PKC). Native HMGB1 extracted from tumour cells inhibits replication and this effect is reduced upon acetylation and completely abolished upon removal of the acidic C-terminal tail. Recombinant HMGB1, however, fails to inhibit replication but it acquires such a property following in vitro phosphorylation by PKC.</description><subject>Acetylation</subject><subject>Acidic tail</subject><subject>Animals</subject><subject>Aphidicolin - pharmacology</subject><subject>DNA replication</subject><subject>DNA Replication - drug effects</subject><subject>DNA, Circular - metabolism</subject><subject>High Mobility Group Proteins - pharmacology</subject><subject>HMGB1 Protein</subject><subject>Humans</subject><subject>Phosphorylation</subject><subject>Protein Kinase C - metabolism</subject><subject>Rats</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Repressor Proteins - pharmacology</subject><subject>Tumor Cells, Cultured</subject><issn>1357-2725</issn><issn>1878-5875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9P3DAQxS1ExZ-l3wAhn7gl9TiJ7eWARCmFSrS90GstrzMRs8rGW9uLxLevV1mpt55mNPPejN6PsUsQNQhQn9b1ioLHsZZC6BqgFtAesTMw2lSd0d1x6ZtOV1LL7pSdp7QWQkAnmxN2CgaWoECesd9P3x8_A9_GkJEmTtMrrSgn_uXHHY-4Hcm7TGG_4G-UY7jhZR5G5GHg-RW585jfx1njpv4wo548z47GC_ZhcGPCj4e6YL--PrzcP1XPPx-_3d89V75RIleuHzQ4rxCFdCDV0C-1cMorL7EznVmBcar1WhovmraFbljq1hstpShWbJoFu57vliB_dpiy3VAqcEY3Ydglq5agW13CL1g7C30MKUUc7DbSxsV3C8Luudq1nbnaPVcLYAvXYrs63N-tNtj_Mx1AFsHtLMCS8o0w2uQJJ489RfTZ9oH-_-EvdaGJ_Q</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Topalova, Dessislava</creator><creator>Ugrinova, Iva</creator><creator>Pashev, Iliya G.</creator><creator>Pasheva, Evdokia A.</creator><general>Elsevier Ltd</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></search><sort><creationdate>2008</creationdate><title>HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail</title><author>Topalova, Dessislava ; Ugrinova, Iva ; Pashev, Iliya G. ; Pasheva, Evdokia A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-adf71ac6ee02a126fd970a6c6c2e5858b18a64c728c034415f974c87220adfe33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acetylation</topic><topic>Acidic tail</topic><topic>Animals</topic><topic>Aphidicolin - pharmacology</topic><topic>DNA replication</topic><topic>DNA Replication - drug effects</topic><topic>DNA, Circular - metabolism</topic><topic>High Mobility Group Proteins - pharmacology</topic><topic>HMGB1 Protein</topic><topic>Humans</topic><topic>Phosphorylation</topic><topic>Protein Kinase C - metabolism</topic><topic>Rats</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Repressor Proteins - pharmacology</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Topalova, Dessislava</creatorcontrib><creatorcontrib>Ugrinova, Iva</creatorcontrib><creatorcontrib>Pashev, Iliya G.</creatorcontrib><creatorcontrib>Pasheva, Evdokia A.</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><jtitle>The international journal of biochemistry &amp; cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Topalova, Dessislava</au><au>Ugrinova, Iva</au><au>Pashev, Iliya G.</au><au>Pasheva, Evdokia A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail</atitle><jtitle>The international journal of biochemistry &amp; cell biology</jtitle><addtitle>Int J Biochem Cell Biol</addtitle><date>2008</date><risdate>2008</risdate><volume>40</volume><issue>8</issue><spage>1536</spage><epage>1542</epage><pages>1536-1542</pages><issn>1357-2725</issn><eissn>1878-5875</eissn><abstract>The high mobility group box (HMGB) 1 protein is a very abundant and conserved protein that is implicated in many key cellular events but its functions within the nucleus remain elusive. The role of this protein in replication of closed circular DNA containing a eukaryotic origin of replication has been studied in vitro by using native and recombinant HMGB1 as well as various modified HMGB1 preparations such as truncated protein, lacking its C-terminal tail, in vivo acetylated protein, and recombinant HMGB1 phosphorylated in vitro by protein kinase C (PKC). Native HMGB1 extracted from tumour cells inhibits replication and this effect is reduced upon acetylation and completely abolished upon removal of the acidic C-terminal tail. Recombinant HMGB1, however, fails to inhibit replication but it acquires such a property following in vitro phosphorylation by PKC.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>18191612</pmid><doi>10.1016/j.biocel.2007.11.014</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1357-2725
ispartof The international journal of biochemistry & cell biology, 2008, Vol.40 (8), p.1536-1542
issn 1357-2725
1878-5875
language eng
recordid cdi_proquest_miscellaneous_69174752
source MEDLINE; Elsevier ScienceDirect Journals
subjects Acetylation
Acidic tail
Animals
Aphidicolin - pharmacology
DNA replication
DNA Replication - drug effects
DNA, Circular - metabolism
High Mobility Group Proteins - pharmacology
HMGB1 Protein
Humans
Phosphorylation
Protein Kinase C - metabolism
Rats
Recombinant Proteins - pharmacology
Repressor Proteins - pharmacology
Tumor Cells, Cultured
title HMGB1 protein inhibits DNA replication in vitro: A role of the acetylation and the acidic tail
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T12%3A43%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=HMGB1%20protein%20inhibits%20DNA%20replication%20in%20vitro:%20A%20role%20of%20the%20acetylation%20and%20the%20acidic%20tail&rft.jtitle=The%20international%20journal%20of%20biochemistry%20&%20cell%20biology&rft.au=Topalova,%20Dessislava&rft.date=2008&rft.volume=40&rft.issue=8&rft.spage=1536&rft.epage=1542&rft.pages=1536-1542&rft.issn=1357-2725&rft.eissn=1878-5875&rft_id=info:doi/10.1016/j.biocel.2007.11.014&rft_dat=%3Cproquest_cross%3E69174752%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=69174752&rft_id=info:pmid/18191612&rft_els_id=S1357272507003986&rfr_iscdi=true