In vivo dynamics and kinetics of pKi-67: Transition from a mobile to an immobile form at the onset of anaphase
A cell proliferation marker protein, pKi-67, distributes to the chromosome periphery during mitosis and nucleolar heterochromatin in the interphase. We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain we...
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description | A cell proliferation marker protein, pKi-67, distributes to the chromosome periphery during mitosis and nucleolar heterochromatin in the interphase. We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain were involved in localization to the nucleolar heterochromatin, both the LR domain and the Ki-67 repeat domain were required for its distribution to the mitotic chromosome periphery. Using in vivo time-lapse microscopy, GFP-pKi-67 was dynamically tracked from the mitotic chromosome periphery to reforming nucleoli via prenucleolar bodies (PNBs). The signals in PNBs then moved towards and fused into the reforming nucleoli with a thin string-like fluorescence during early G1 phase. An analysis of the in vivo kinetics of pKi-67 using photobleaching indicated that the association of pKi-67 with chromatin was progressively altered from “loose” to “tight” after the onset of anaphase. These findings indicate that pKi-67 dynamically alters the nature of the interaction with chromatin structure during the cell cycle, which is closely related to the reformation process of the interphase nucleolar chromatin. |
doi_str_mv | 10.1016/j.yexcr.2005.04.010 |
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We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain were involved in localization to the nucleolar heterochromatin, both the LR domain and the Ki-67 repeat domain were required for its distribution to the mitotic chromosome periphery. Using in vivo time-lapse microscopy, GFP-pKi-67 was dynamically tracked from the mitotic chromosome periphery to reforming nucleoli via prenucleolar bodies (PNBs). The signals in PNBs then moved towards and fused into the reforming nucleoli with a thin string-like fluorescence during early G1 phase. An analysis of the in vivo kinetics of pKi-67 using photobleaching indicated that the association of pKi-67 with chromatin was progressively altered from “loose” to “tight” after the onset of anaphase. These findings indicate that pKi-67 dynamically alters the nature of the interaction with chromatin structure during the cell cycle, which is closely related to the reformation process of the interphase nucleolar chromatin.</description><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/j.yexcr.2005.04.010</identifier><identifier>PMID: 15896774</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Anaphase - physiology ; CELL CYCLE ; CELL PROLIFERATION ; Chromatin ; Chromatin - physiology ; Chromosome periphery ; CHROMOSOMES ; Chromosomes, Human - chemistry ; Chromosomes, Human - physiology ; FLUORESCENCE ; Green Fluorescent Proteins - chemistry ; Green Fluorescent Proteins - physiology ; HeLa Cells ; HETEROCHROMATIN ; Humans ; IN VIVO ; Ki-67 Antigen - chemistry ; Ki-67 Antigen - metabolism ; KINETICS ; Live cell imaging ; MICROSCOPY ; MITOSIS ; Mitosis - physiology ; Movement - physiology ; NUCLEOLI ; pKi-67 ; Protein Transport - genetics ; Protein Transport - physiology ; PROTEINS</subject><ispartof>Experimental cell research, 2005-08, Vol.308 (1), p.123-134</ispartof><rights>2005 Elsevier Inc.</rights><rights>Copyright © 2005 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-e3b2571cc7303f7db8534879e50bf0c30acfd3192625650a444c2040e5e6b8593</citedby><cites>FETCH-LOGICAL-c509t-e3b2571cc7303f7db8534879e50bf0c30acfd3192625650a444c2040e5e6b8593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014482705001606$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15896774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/20717635$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Saiwaki, Takuya</creatorcontrib><creatorcontrib>Kotera, Ippei</creatorcontrib><creatorcontrib>Sasaki, Mitsuho</creatorcontrib><creatorcontrib>Takagi, Masatoshi</creatorcontrib><creatorcontrib>Yoneda, Yoshihiro</creatorcontrib><title>In vivo dynamics and kinetics of pKi-67: Transition from a mobile to an immobile form at the onset of anaphase</title><title>Experimental cell research</title><addtitle>Exp Cell Res</addtitle><description>A cell proliferation marker protein, pKi-67, distributes to the chromosome periphery during mitosis and nucleolar heterochromatin in the interphase. We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain were involved in localization to the nucleolar heterochromatin, both the LR domain and the Ki-67 repeat domain were required for its distribution to the mitotic chromosome periphery. Using in vivo time-lapse microscopy, GFP-pKi-67 was dynamically tracked from the mitotic chromosome periphery to reforming nucleoli via prenucleolar bodies (PNBs). The signals in PNBs then moved towards and fused into the reforming nucleoli with a thin string-like fluorescence during early G1 phase. An analysis of the in vivo kinetics of pKi-67 using photobleaching indicated that the association of pKi-67 with chromatin was progressively altered from “loose” to “tight” after the onset of anaphase. These findings indicate that pKi-67 dynamically alters the nature of the interaction with chromatin structure during the cell cycle, which is closely related to the reformation process of the interphase nucleolar chromatin.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Anaphase - physiology</subject><subject>CELL CYCLE</subject><subject>CELL PROLIFERATION</subject><subject>Chromatin</subject><subject>Chromatin - physiology</subject><subject>Chromosome periphery</subject><subject>CHROMOSOMES</subject><subject>Chromosomes, Human - chemistry</subject><subject>Chromosomes, Human - physiology</subject><subject>FLUORESCENCE</subject><subject>Green Fluorescent Proteins - chemistry</subject><subject>Green Fluorescent Proteins - physiology</subject><subject>HeLa Cells</subject><subject>HETEROCHROMATIN</subject><subject>Humans</subject><subject>IN VIVO</subject><subject>Ki-67 Antigen - chemistry</subject><subject>Ki-67 Antigen - metabolism</subject><subject>KINETICS</subject><subject>Live cell imaging</subject><subject>MICROSCOPY</subject><subject>MITOSIS</subject><subject>Mitosis - physiology</subject><subject>Movement - physiology</subject><subject>NUCLEOLI</subject><subject>pKi-67</subject><subject>Protein Transport - genetics</subject><subject>Protein Transport - physiology</subject><subject>PROTEINS</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhQtRnHb0FwgSFNxVe_OuElzI4GNwwM24DqnULTptV9Im6cb-96bsBsGFrsIl3zmXe07TPKewpkDVm-36hD9dWjMAuQaxBgoPmhWFHlomGHvYrACoaEXH9FXzJOctAHQdVY-bKyq7XmktVk24DeToj5GMp2Bn7zKxYSTffcCyDHEi-y--VfotuU82ZF98DGRKcSaWzHHwOyQlVg3x82WcYqqfhZQNkhgylsXEBrvf2IxPm0eT3WV8dnmvm28fP9zffG7vvn66vXl_1zoJfWmRD0xq6pzmwCc9Dp3kotM9ShgmcBysm0ZOe6aYVBKsEMIxEIASVWV7ft28OvvGXLzJzhd0GxdDQFcMA0214rJSr8_UPsUfB8zFzD473O1swHjIRnVQk1L_B6sjr3GqCr78C9zGQwr1VEN7oToOjFaInyGXYs4JJ7NPfrbpZCiYpVqzNb-rNUu1BoSp1VbVi4v1YZhx_KO5dFmBd2cAa7BHj2m5G4PD0afl7DH6fy74BV7Hsxw</recordid><startdate>20050801</startdate><enddate>20050801</enddate><creator>Saiwaki, Takuya</creator><creator>Kotera, Ippei</creator><creator>Sasaki, Mitsuho</creator><creator>Takagi, Masatoshi</creator><creator>Yoneda, Yoshihiro</creator><general>Elsevier Inc</general><general>Elsevier BV</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>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>20050801</creationdate><title>In vivo dynamics and kinetics of pKi-67: Transition from a mobile to an immobile form at the onset of anaphase</title><author>Saiwaki, Takuya ; Kotera, Ippei ; Sasaki, Mitsuho ; Takagi, Masatoshi ; Yoneda, Yoshihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-e3b2571cc7303f7db8534879e50bf0c30acfd3192625650a444c2040e5e6b8593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Anaphase - physiology</topic><topic>CELL CYCLE</topic><topic>CELL PROLIFERATION</topic><topic>Chromatin</topic><topic>Chromatin - physiology</topic><topic>Chromosome periphery</topic><topic>CHROMOSOMES</topic><topic>Chromosomes, Human - chemistry</topic><topic>Chromosomes, Human - physiology</topic><topic>FLUORESCENCE</topic><topic>Green Fluorescent Proteins - chemistry</topic><topic>Green Fluorescent Proteins - physiology</topic><topic>HeLa Cells</topic><topic>HETEROCHROMATIN</topic><topic>Humans</topic><topic>IN VIVO</topic><topic>Ki-67 Antigen - chemistry</topic><topic>Ki-67 Antigen - metabolism</topic><topic>KINETICS</topic><topic>Live cell imaging</topic><topic>MICROSCOPY</topic><topic>MITOSIS</topic><topic>Mitosis - physiology</topic><topic>Movement - physiology</topic><topic>NUCLEOLI</topic><topic>pKi-67</topic><topic>Protein Transport - genetics</topic><topic>Protein Transport - physiology</topic><topic>PROTEINS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saiwaki, Takuya</creatorcontrib><creatorcontrib>Kotera, Ippei</creatorcontrib><creatorcontrib>Sasaki, Mitsuho</creatorcontrib><creatorcontrib>Takagi, Masatoshi</creatorcontrib><creatorcontrib>Yoneda, Yoshihiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saiwaki, Takuya</au><au>Kotera, Ippei</au><au>Sasaki, Mitsuho</au><au>Takagi, Masatoshi</au><au>Yoneda, Yoshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo dynamics and kinetics of pKi-67: Transition from a mobile to an immobile form at the onset of anaphase</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>2005-08-01</date><risdate>2005</risdate><volume>308</volume><issue>1</issue><spage>123</spage><epage>134</epage><pages>123-134</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><abstract>A cell proliferation marker protein, pKi-67, distributes to the chromosome periphery during mitosis and nucleolar heterochromatin in the interphase. We report here on the structural domains of pKi-67 that are required for its correct distribution. While both the LR domain and the conserved domain were involved in localization to the nucleolar heterochromatin, both the LR domain and the Ki-67 repeat domain were required for its distribution to the mitotic chromosome periphery. Using in vivo time-lapse microscopy, GFP-pKi-67 was dynamically tracked from the mitotic chromosome periphery to reforming nucleoli via prenucleolar bodies (PNBs). The signals in PNBs then moved towards and fused into the reforming nucleoli with a thin string-like fluorescence during early G1 phase. An analysis of the in vivo kinetics of pKi-67 using photobleaching indicated that the association of pKi-67 with chromatin was progressively altered from “loose” to “tight” after the onset of anaphase. These findings indicate that pKi-67 dynamically alters the nature of the interaction with chromatin structure during the cell cycle, which is closely related to the reformation process of the interphase nucleolar chromatin.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15896774</pmid><doi>10.1016/j.yexcr.2005.04.010</doi><tpages>12</tpages></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES Anaphase - physiology CELL CYCLE CELL PROLIFERATION Chromatin Chromatin - physiology Chromosome periphery CHROMOSOMES Chromosomes, Human - chemistry Chromosomes, Human - physiology FLUORESCENCE Green Fluorescent Proteins - chemistry Green Fluorescent Proteins - physiology HeLa Cells HETEROCHROMATIN Humans IN VIVO Ki-67 Antigen - chemistry Ki-67 Antigen - metabolism KINETICS Live cell imaging MICROSCOPY MITOSIS Mitosis - physiology Movement - physiology NUCLEOLI pKi-67 Protein Transport - genetics Protein Transport - physiology PROTEINS |
title | In vivo dynamics and kinetics of pKi-67: Transition from a mobile to an immobile form at the onset of anaphase |
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