Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase
The fluctuations in the expression of two forms of DNA topoisomerase II, p170 and p180, were examined by immunoblotting during the transition of the growth state and the cell cycle in Swiss 3T3 cells. The level of p170 expression was higher during the exponentially growing phase than in the stationa...
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Veröffentlicht in: | The Journal of biological chemistry 1994-01, Vol.269 (2), p.1173-1176 |
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description | The fluctuations in the expression of two forms of DNA topoisomerase II, p170 and p180, were examined by immunoblotting during
the transition of the growth state and the cell cycle in Swiss 3T3 cells. The level of p170 expression was higher during the
exponentially growing phase than in the stationary phase, and the level of p180 did not appear to change when the cells changed
the growth state. When quiescent cells were stimulated with serum, the p170 level began to increase at 12 h and reached a
maximal level at 24-28 h, corresponding to the G2 phase. In contrast, the level of p180 was almost constant during the cell
cycle, and the p180 band became obscure when the number of mitotic cells increased. Immunoblotting of the samples prepared
from metaphase-synchronized HeLa cells did not have a p180 band, but did exhibit a band with a higher molecular weight. This
band increased and p180 decreased in parallel with the increase in the number of mitotic cells. When the cells exited from
the M phase, p180 reappeared and the higher molecular weight band disappeared. |
doi_str_mv | 10.1016/S0021-9258(17)42238-1 |
format | Article |
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the transition of the growth state and the cell cycle in Swiss 3T3 cells. The level of p170 expression was higher during the
exponentially growing phase than in the stationary phase, and the level of p180 did not appear to change when the cells changed
the growth state. When quiescent cells were stimulated with serum, the p170 level began to increase at 12 h and reached a
maximal level at 24-28 h, corresponding to the G2 phase. In contrast, the level of p180 was almost constant during the cell
cycle, and the p180 band became obscure when the number of mitotic cells increased. Immunoblotting of the samples prepared
from metaphase-synchronized HeLa cells did not have a p180 band, but did exhibit a band with a higher molecular weight. This
band increased and p180 decreased in parallel with the increase in the number of mitotic cells. When the cells exited from
the M phase, p180 reappeared and the higher molecular weight band disappeared.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(17)42238-1</identifier><identifier>PMID: 8288578</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Biochemistry and Molecular Biology</publisher><subject>3T3 Cells ; Analytical, structural and metabolic biochemistry ; Animals ; Aphidicolin - pharmacology ; Biological and medical sciences ; Cell Compartmentation ; Cell Cycle - drug effects ; DNA Topoisomerases, Type II - chemistry ; DNA Topoisomerases, Type II - metabolism ; Enzymes and enzyme inhibitors ; Fundamental and applied biological sciences. Psychology ; HeLa Cells ; Humans ; Isoenzymes - metabolism ; Isomerases ; Mice ; Mitosis ; Molecular Weight</subject><ispartof>The Journal of biological chemistry, 1994-01, Vol.269 (2), p.1173-1176</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3531-5d2732e73822f698e907b59e704c3a324aedc7a5fc6028b329bd0943eabb15873</citedby><cites>FETCH-LOGICAL-c3531-5d2732e73822f698e907b59e704c3a324aedc7a5fc6028b329bd0943eabb15873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3953530$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8288578$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KIMURA, K</creatorcontrib><creatorcontrib>SAIJO, M</creatorcontrib><creatorcontrib>UI, M</creatorcontrib><creatorcontrib>ENOMOTO, T</creatorcontrib><title>Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The fluctuations in the expression of two forms of DNA topoisomerase II, p170 and p180, were examined by immunoblotting during
the transition of the growth state and the cell cycle in Swiss 3T3 cells. The level of p170 expression was higher during the
exponentially growing phase than in the stationary phase, and the level of p180 did not appear to change when the cells changed
the growth state. When quiescent cells were stimulated with serum, the p170 level began to increase at 12 h and reached a
maximal level at 24-28 h, corresponding to the G2 phase. In contrast, the level of p180 was almost constant during the cell
cycle, and the p180 band became obscure when the number of mitotic cells increased. Immunoblotting of the samples prepared
from metaphase-synchronized HeLa cells did not have a p180 band, but did exhibit a band with a higher molecular weight. This
band increased and p180 decreased in parallel with the increase in the number of mitotic cells. When the cells exited from
the M phase, p180 reappeared and the higher molecular weight band disappeared.</description><subject>3T3 Cells</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Aphidicolin - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell Compartmentation</subject><subject>Cell Cycle - drug effects</subject><subject>DNA Topoisomerases, Type II - chemistry</subject><subject>DNA Topoisomerases, Type II - metabolism</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Isoenzymes - metabolism</subject><subject>Isomerases</subject><subject>Mice</subject><subject>Mitosis</subject><subject>Molecular Weight</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2O1DAQhS0EGpqGI4xkIYRgEfBPHDvL0QBDSwMsAImd5TgVYpTEGdtRM6fjajjdTW_xpuSqV19J7yF0SckbSmj19ishjBY1E-oVla9Lxrgq6AO0oUTxggv64yHanCWP0ZMYf5H8yppeoAvFlBJSbdCfm-D3qccxmQQFNlOLLQwDtvd2gKKFGaYWpoS7YbFpMcn5CbsJpx4w_J4DxLh2fIfT3uPOhzGun3efr3Dys3fRjxBMBLzbHdizzwvNADjOYF3nLB59u9YjeeVkcu9-9hDyaAC7DCbgPeROOvD_Xf-E5z6Dn6JHnRkiPDvVLfr-4f2364_F7Zeb3fXVbWG54LQQLZOcgeSKsa6qFdRENqIGSUrLDWelgdZKIzpbEaYazuqmJXXJwTQNFUryLXp55M7B3y0Qkx5dXJ0yE_glallxLjkR_xXSSlaKZ_kWiaPQhmxKgE7PwY0m3GtK9JqwPiSs1_g0lfqQsKZ57_J0YGlGaM9bp0jz_MVpbqI1QxfMZF08y3gtsiMky54fZavZexdAN87bHkbNqlozTank_C9xebw7</recordid><startdate>19940114</startdate><enddate>19940114</enddate><creator>KIMURA, K</creator><creator>SAIJO, M</creator><creator>UI, M</creator><creator>ENOMOTO, T</creator><general>American Society for Biochemistry and Molecular Biology</general><scope>IQODW</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>19940114</creationdate><title>Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase</title><author>KIMURA, K ; SAIJO, M ; UI, M ; ENOMOTO, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3531-5d2732e73822f698e907b59e704c3a324aedc7a5fc6028b329bd0943eabb15873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>3T3 Cells</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Aphidicolin - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell Compartmentation</topic><topic>Cell Cycle - drug effects</topic><topic>DNA Topoisomerases, Type II - chemistry</topic><topic>DNA Topoisomerases, Type II - metabolism</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Isoenzymes - metabolism</topic><topic>Isomerases</topic><topic>Mice</topic><topic>Mitosis</topic><topic>Molecular Weight</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KIMURA, K</creatorcontrib><creatorcontrib>SAIJO, M</creatorcontrib><creatorcontrib>UI, M</creatorcontrib><creatorcontrib>ENOMOTO, T</creatorcontrib><collection>Pascal-Francis</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>KIMURA, K</au><au>SAIJO, M</au><au>UI, M</au><au>ENOMOTO, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1994-01-14</date><risdate>1994</risdate><volume>269</volume><issue>2</issue><spage>1173</spage><epage>1176</epage><pages>1173-1176</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>The fluctuations in the expression of two forms of DNA topoisomerase II, p170 and p180, were examined by immunoblotting during
the transition of the growth state and the cell cycle in Swiss 3T3 cells. The level of p170 expression was higher during the
exponentially growing phase than in the stationary phase, and the level of p180 did not appear to change when the cells changed
the growth state. When quiescent cells were stimulated with serum, the p170 level began to increase at 12 h and reached a
maximal level at 24-28 h, corresponding to the G2 phase. In contrast, the level of p180 was almost constant during the cell
cycle, and the p180 band became obscure when the number of mitotic cells increased. Immunoblotting of the samples prepared
from metaphase-synchronized HeLa cells did not have a p180 band, but did exhibit a band with a higher molecular weight. This
band increased and p180 decreased in parallel with the increase in the number of mitotic cells. When the cells exited from
the M phase, p180 reappeared and the higher molecular weight band disappeared.</abstract><cop>Bethesda, MD</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>8288578</pmid><doi>10.1016/S0021-9258(17)42238-1</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | 3T3 Cells Analytical, structural and metabolic biochemistry Animals Aphidicolin - pharmacology Biological and medical sciences Cell Compartmentation Cell Cycle - drug effects DNA Topoisomerases, Type II - chemistry DNA Topoisomerases, Type II - metabolism Enzymes and enzyme inhibitors Fundamental and applied biological sciences. Psychology HeLa Cells Humans Isoenzymes - metabolism Isomerases Mice Mitosis Molecular Weight |
title | Growth state- and cell cycle-dependent fluctuation in the expression of two forms of DNA topoisomerase II and possible specific modification of the higher molecular weight form in the M phase |
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