Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle
We characterized changes of nucleosome assembly activity, intracellular localization, and reversible phosphorylation of the human chromatin assembly factor CAF-1 during the somatic cell division cycle. HeLa cells were synchronized in the G1, S, G2, and M phases of the cell cycle. All three subunits...
Gespeichert in:
Veröffentlicht in: | The Journal of biological chemistry 1998-06, Vol.273 (24), p.15279-15286 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15286 |
---|---|
container_issue | 24 |
container_start_page | 15279 |
container_title | The Journal of biological chemistry |
container_volume | 273 |
creator | Marheineke, Kathrin Krude, Torsten |
description | We characterized changes of nucleosome assembly activity, intracellular localization, and reversible phosphorylation of the human chromatin assembly factor CAF-1 during the somatic cell division cycle. HeLa cells were synchronized in the G1, S, G2, and M phases of the cell cycle. All three subunits of human CAF-1 (p150, p60, and p48) are present during the entire cell cycle. In interphase, p150 and p60 are bound to the nucleus, but they predominantly dissociate from chromatin during mitosis. During S phase, p150 and p60 are concentrated at sites of intranuclear DNA replication. Only a fraction of total p48 is associated with p150 and p60, and the majority is present in other high molecular weight complexes. The other nucleosome assembly protein, NAP-1, is predominantly cytosolic throughout the cell cycle. Human CAF-1 efficiently mediates nucleosome assembly during complementary DNA strand synthesis in G1, S, and G2 phase cytosolic extracts. Active CAF-1 can be isolated as a 6.5 S complex from G1, S, and G2phase nuclei. In contrast, CAF-1 isolated from mitotic cytosol does not support nucleosome assembly during DNA synthesis. In mitosis, the p60 subunit of inactive CAF-1 is hyperphosphorylated, whereas active CAF-1 in interphase contains hypophosphorylated and/or phosphorylated forms of p60. |
doi_str_mv | 10.1074/jbc.273.24.15279 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79922730</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925819654190</els_id><sourcerecordid>79922730</sourcerecordid><originalsourceid>FETCH-LOGICAL-c513t-fe5bdac64bebbee0da752f094d5e457c555b86b8eb5f41c0c5d9a440d4b8275c3</originalsourceid><addsrcrecordid>eNqFkb1v2zAUxImiQeq42bsU4FB0k0NSpCV1M9SmCWAkSwpkI_jxZNGQxISUErh_feja6BAgCBcO73fHxzuEvlCyoKTgF1ttFqzIF4wvqGBF9QHNKCnzLBf0_iOaEcJoVjFRfkJnMW5JOryip-i0WlJOOZ-hx5vJdOCj7wGvYoRedzu8MqN7cuMOq8Hi62EMykDXTZ0KeO2N6txfNTo_YN_gq6lXA65XlxnFdauGDURsp-CGDR5bwHXS4Z_JLO75epfe-oxOGtVFOD_ec_Tn8tddfZWtb39f16t1ZgTNx6wBoa0yS65BawBiVSFYQypuBXBRGCGELpe6BC0aTg0xwlaKc2K5LlkhTD5H3w--D8E_ThBH2bu4_4cawE9RFlXFUnTkXZAuhchZyRNIDqAJPsYAjXwIrldhJymR-zpkqkMmT8m4_FdHknw9ek-6B_tfcMw_zb8d5q3btM8ugNTOmxb61zY_DhikwJ4cBBmNg8GATRIzSuvd2zu8ANHGpnQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16553284</pqid></control><display><type>article</type><title>Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Marheineke, Kathrin ; Krude, Torsten</creator><creatorcontrib>Marheineke, Kathrin ; Krude, Torsten</creatorcontrib><description>We characterized changes of nucleosome assembly activity, intracellular localization, and reversible phosphorylation of the human chromatin assembly factor CAF-1 during the somatic cell division cycle. HeLa cells were synchronized in the G1, S, G2, and M phases of the cell cycle. All three subunits of human CAF-1 (p150, p60, and p48) are present during the entire cell cycle. In interphase, p150 and p60 are bound to the nucleus, but they predominantly dissociate from chromatin during mitosis. During S phase, p150 and p60 are concentrated at sites of intranuclear DNA replication. Only a fraction of total p48 is associated with p150 and p60, and the majority is present in other high molecular weight complexes. The other nucleosome assembly protein, NAP-1, is predominantly cytosolic throughout the cell cycle. Human CAF-1 efficiently mediates nucleosome assembly during complementary DNA strand synthesis in G1, S, and G2 phase cytosolic extracts. Active CAF-1 can be isolated as a 6.5 S complex from G1, S, and G2phase nuclei. In contrast, CAF-1 isolated from mitotic cytosol does not support nucleosome assembly during DNA synthesis. In mitosis, the p60 subunit of inactive CAF-1 is hyperphosphorylated, whereas active CAF-1 in interphase contains hypophosphorylated and/or phosphorylated forms of p60.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.273.24.15279</identifier><identifier>PMID: 9614144</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cell Cycle - physiology ; Cell Cycle Proteins ; Chromatin - metabolism ; Chromatin Assembly Factor-1 ; Chromosomal Proteins, Non-Histone ; DNA Replication - physiology ; DNA-Binding Proteins - chemistry ; Flow Cytometry ; HeLa Cells ; Humans ; Micrococcal Nuclease - metabolism ; Mitosis - physiology ; Nuclear Proteins - analysis ; Nucleosome Assembly Protein 1 ; Nucleosomes - metabolism ; Phosphorylation ; Proteins - metabolism ; Transcription Factors</subject><ispartof>The Journal of biological chemistry, 1998-06, Vol.273 (24), p.15279-15286</ispartof><rights>1998 © 1998 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-fe5bdac64bebbee0da752f094d5e457c555b86b8eb5f41c0c5d9a440d4b8275c3</citedby><cites>FETCH-LOGICAL-c513t-fe5bdac64bebbee0da752f094d5e457c555b86b8eb5f41c0c5d9a440d4b8275c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9614144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marheineke, Kathrin</creatorcontrib><creatorcontrib>Krude, Torsten</creatorcontrib><title>Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>We characterized changes of nucleosome assembly activity, intracellular localization, and reversible phosphorylation of the human chromatin assembly factor CAF-1 during the somatic cell division cycle. HeLa cells were synchronized in the G1, S, G2, and M phases of the cell cycle. All three subunits of human CAF-1 (p150, p60, and p48) are present during the entire cell cycle. In interphase, p150 and p60 are bound to the nucleus, but they predominantly dissociate from chromatin during mitosis. During S phase, p150 and p60 are concentrated at sites of intranuclear DNA replication. Only a fraction of total p48 is associated with p150 and p60, and the majority is present in other high molecular weight complexes. The other nucleosome assembly protein, NAP-1, is predominantly cytosolic throughout the cell cycle. Human CAF-1 efficiently mediates nucleosome assembly during complementary DNA strand synthesis in G1, S, and G2 phase cytosolic extracts. Active CAF-1 can be isolated as a 6.5 S complex from G1, S, and G2phase nuclei. In contrast, CAF-1 isolated from mitotic cytosol does not support nucleosome assembly during DNA synthesis. In mitosis, the p60 subunit of inactive CAF-1 is hyperphosphorylated, whereas active CAF-1 in interphase contains hypophosphorylated and/or phosphorylated forms of p60.</description><subject>Cell Cycle - physiology</subject><subject>Cell Cycle Proteins</subject><subject>Chromatin - metabolism</subject><subject>Chromatin Assembly Factor-1</subject><subject>Chromosomal Proteins, Non-Histone</subject><subject>DNA Replication - physiology</subject><subject>DNA-Binding Proteins - chemistry</subject><subject>Flow Cytometry</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Micrococcal Nuclease - metabolism</subject><subject>Mitosis - physiology</subject><subject>Nuclear Proteins - analysis</subject><subject>Nucleosome Assembly Protein 1</subject><subject>Nucleosomes - metabolism</subject><subject>Phosphorylation</subject><subject>Proteins - metabolism</subject><subject>Transcription Factors</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb1v2zAUxImiQeq42bsU4FB0k0NSpCV1M9SmCWAkSwpkI_jxZNGQxISUErh_feja6BAgCBcO73fHxzuEvlCyoKTgF1ttFqzIF4wvqGBF9QHNKCnzLBf0_iOaEcJoVjFRfkJnMW5JOryip-i0WlJOOZ-hx5vJdOCj7wGvYoRedzu8MqN7cuMOq8Hi62EMykDXTZ0KeO2N6txfNTo_YN_gq6lXA65XlxnFdauGDURsp-CGDR5bwHXS4Z_JLO75epfe-oxOGtVFOD_ec_Tn8tddfZWtb39f16t1ZgTNx6wBoa0yS65BawBiVSFYQypuBXBRGCGELpe6BC0aTg0xwlaKc2K5LlkhTD5H3w--D8E_ThBH2bu4_4cawE9RFlXFUnTkXZAuhchZyRNIDqAJPsYAjXwIrldhJymR-zpkqkMmT8m4_FdHknw9ek-6B_tfcMw_zb8d5q3btM8ugNTOmxb61zY_DhikwJ4cBBmNg8GATRIzSuvd2zu8ANHGpnQ</recordid><startdate>19980612</startdate><enddate>19980612</enddate><creator>Marheineke, Kathrin</creator><creator>Krude, Torsten</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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>7X8</scope></search><sort><creationdate>19980612</creationdate><title>Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle</title><author>Marheineke, Kathrin ; Krude, Torsten</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-fe5bdac64bebbee0da752f094d5e457c555b86b8eb5f41c0c5d9a440d4b8275c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Cell Cycle - physiology</topic><topic>Cell Cycle Proteins</topic><topic>Chromatin - metabolism</topic><topic>Chromatin Assembly Factor-1</topic><topic>Chromosomal Proteins, Non-Histone</topic><topic>DNA Replication - physiology</topic><topic>DNA-Binding Proteins - chemistry</topic><topic>Flow Cytometry</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Micrococcal Nuclease - metabolism</topic><topic>Mitosis - physiology</topic><topic>Nuclear Proteins - analysis</topic><topic>Nucleosome Assembly Protein 1</topic><topic>Nucleosomes - metabolism</topic><topic>Phosphorylation</topic><topic>Proteins - metabolism</topic><topic>Transcription Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marheineke, Kathrin</creatorcontrib><creatorcontrib>Krude, Torsten</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marheineke, Kathrin</au><au>Krude, Torsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1998-06-12</date><risdate>1998</risdate><volume>273</volume><issue>24</issue><spage>15279</spage><epage>15286</epage><pages>15279-15286</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>We characterized changes of nucleosome assembly activity, intracellular localization, and reversible phosphorylation of the human chromatin assembly factor CAF-1 during the somatic cell division cycle. HeLa cells were synchronized in the G1, S, G2, and M phases of the cell cycle. All three subunits of human CAF-1 (p150, p60, and p48) are present during the entire cell cycle. In interphase, p150 and p60 are bound to the nucleus, but they predominantly dissociate from chromatin during mitosis. During S phase, p150 and p60 are concentrated at sites of intranuclear DNA replication. Only a fraction of total p48 is associated with p150 and p60, and the majority is present in other high molecular weight complexes. The other nucleosome assembly protein, NAP-1, is predominantly cytosolic throughout the cell cycle. Human CAF-1 efficiently mediates nucleosome assembly during complementary DNA strand synthesis in G1, S, and G2 phase cytosolic extracts. Active CAF-1 can be isolated as a 6.5 S complex from G1, S, and G2phase nuclei. In contrast, CAF-1 isolated from mitotic cytosol does not support nucleosome assembly during DNA synthesis. In mitosis, the p60 subunit of inactive CAF-1 is hyperphosphorylated, whereas active CAF-1 in interphase contains hypophosphorylated and/or phosphorylated forms of p60.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9614144</pmid><doi>10.1074/jbc.273.24.15279</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9258 |
ispartof | The Journal of biological chemistry, 1998-06, Vol.273 (24), p.15279-15286 |
issn | 0021-9258 1083-351X |
language | eng |
recordid | cdi_proquest_miscellaneous_79922730 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Cell Cycle - physiology Cell Cycle Proteins Chromatin - metabolism Chromatin Assembly Factor-1 Chromosomal Proteins, Non-Histone DNA Replication - physiology DNA-Binding Proteins - chemistry Flow Cytometry HeLa Cells Humans Micrococcal Nuclease - metabolism Mitosis - physiology Nuclear Proteins - analysis Nucleosome Assembly Protein 1 Nucleosomes - metabolism Phosphorylation Proteins - metabolism Transcription Factors |
title | Nucleosome Assembly Activity and Intracellular Localization of Human CAF-1 Changes during the Cell Division Cycle |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T00%3A28%3A58IST&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=Nucleosome%20Assembly%20Activity%20and%20Intracellular%20Localization%20of%20Human%20CAF-1%20Changes%20during%20the%20Cell%20Division%20Cycle&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Marheineke,%20Kathrin&rft.date=1998-06-12&rft.volume=273&rft.issue=24&rft.spage=15279&rft.epage=15286&rft.pages=15279-15286&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.273.24.15279&rft_dat=%3Cproquest_cross%3E79922730%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=16553284&rft_id=info:pmid/9614144&rft_els_id=S0021925819654190&rfr_iscdi=true |