Replication-coupled modulation of early replicating chromatin domains detected by anti-actin antibody
Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a monoclonal anti‐actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cy...
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Published in | Journal of cellular biochemistry Vol. 94; no. 5; pp. 899 - 916 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a monoclonal anti‐actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cycle window beginning in early S phase and extending through S phase, G2 phase, mitosis until early G1 phase of the subsequent daughter cells. A small but significant level of co‐localization was measured between the nuclear epiC and active sites of DNA replication in early S phase. The level of co‐localization was strikingly enhanced beginning approximately 1 h after the initial labeling of early S phase replicating chromatin domains. In contrast, epiC did not co‐localize with late S phase replicated chromatin either during DNA replication or at any other time in the cell cycle. We propose a replication‐coupled modulation of early S phase replicated chromatin domains that is detected by the chromatin epiC positivity, persists on the chromatin domains from early S until early G1 of the next cell generation, and may be involved in the regulation and/or coordination of replicational and transcriptional processes during the cell cycle. Further studies will be required to resolve the possible role of nuclear actin in this modulation process. J. Cell. Biochem. 94: 899–916, 2005. © 2005 Wiley‐Liss, Inc. |
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AbstractList | Evidence is presented for the reversible, cold-dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a monoclonal anti-actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cycle window beginning in early S phase and extending through S phase, G sub(2) phase, mitosis until early G sub(1) phase of the subsequent daughter cells. A small but significant level of co-localization was measured between the nuclear epiC and active sites of DNA replication in early S phase. The level of co-localization was strikingly enhanced beginning approximately 1 h after the initial labeling of early S phase replicating chromatin domains. In contrast, epiC did not co- localize with late S phase replicated chromatin either during DNA replication or at any other time in the cell cycle. We propose a replication-coupled modulation of early S phase replicated chromatin domains that is detected by the chromatin epiC positivity, persists on the chromatin domains from early S until early G sub(1) of the next cell generation, and may be involved in the regulation and/or coordination of replicational and transcriptional processes during the cell cycle. Further studies will be required to resolve the possible role of nuclear actin in this modulation process. J. Cell. Biochem. 94: 899-916, 2005. Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a monoclonal anti‐actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cycle window beginning in early S phase and extending through S phase, G2 phase, mitosis until early G1 phase of the subsequent daughter cells. A small but significant level of co‐localization was measured between the nuclear epiC and active sites of DNA replication in early S phase. The level of co‐localization was strikingly enhanced beginning approximately 1 h after the initial labeling of early S phase replicating chromatin domains. In contrast, epiC did not co‐localize with late S phase replicated chromatin either during DNA replication or at any other time in the cell cycle. We propose a replication‐coupled modulation of early S phase replicated chromatin domains that is detected by the chromatin epiC positivity, persists on the chromatin domains from early S until early G1 of the next cell generation, and may be involved in the regulation and/or coordination of replicational and transcriptional processes during the cell cycle. Further studies will be required to resolve the possible role of nuclear actin in this modulation process. J. Cell. Biochem. 94: 899–916, 2005. © 2005 Wiley‐Liss, Inc. Evidence is presented for the reversible, cold-dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a monoclonal anti-actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cycle window beginning in early S phase and extending through S phase, G(2) phase, mitosis until early G(1) phase of the subsequent daughter cells. A small but significant level of co-localization was measured between the nuclear epiC and active sites of DNA replication in early S phase. The level of co-localization was strikingly enhanced beginning approximately 1 h after the initial labeling of early S phase replicating chromatin domains. In contrast, epiC did not co-localize with late S phase replicated chromatin either during DNA replication or at any other time in the cell cycle. We propose a replication-coupled modulation of early S phase replicated chromatin domains that is detected by the chromatin epiC positivity, persists on the chromatin domains from early S until early G(1) of the next cell generation, and may be involved in the regulation and/or coordination of replicational and transcriptional processes during the cell cycle. Further studies will be required to resolve the possible role of nuclear actin in this modulation process. Abstract Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC ), recognized by a monoclonal anti‐actin antibody in diploid human fibroblast cell nuclei and mitotic chromosomes. The nuclear/chromosomal epiC was detected in a cell cycle window beginning in early S phase and extending through S phase, G 2 phase, mitosis until early G 1 phase of the subsequent daughter cells. A small but significant level of co‐localization was measured between the nuclear epiC and active sites of DNA replication in early S phase. The level of co‐localization was strikingly enhanced beginning approximately 1 h after the initial labeling of early S phase replicating chromatin domains. In contrast, epiC did not co‐localize with late S phase replicated chromatin either during DNA replication or at any other time in the cell cycle. We propose a replication‐coupled modulation of early S phase replicated chromatin domains that is detected by the chromatin epiC positivity, persists on the chromatin domains from early S until early G 1 of the next cell generation, and may be involved in the regulation and/or coordination of replicational and transcriptional processes during the cell cycle. Further studies will be required to resolve the possible role of nuclear actin in this modulation process. J. Cell. Biochem. 94: 899–916, 2005. © 2005 Wiley‐Liss, Inc. |
Author | Fialová, Markéta Fidlerová, Helena Berezney, Ronald Malínský, Jan Louz̆ecká, Alena Cvac̆ková, Zuzana Mašata, Martin Koberna, Karel Ras̆ka, Ivan |
Author_xml | – sequence: 1 givenname: Helena surname: Fidlerová fullname: Fidlerová, Helena email: hfidl@lf1.cuni.cz organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 2 givenname: Martin surname: Mašata fullname: Mašata, Martin organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 3 givenname: Jan surname: Malínský fullname: Malínský, Jan organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 4 givenname: Markéta surname: Fialová fullname: Fialová, Markéta organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 5 givenname: Zuzana surname: Cvac̆ková fullname: Cvac̆ková, Zuzana organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 6 givenname: Alena surname: Louz̆ecká fullname: Louz̆ecká, Alena organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 7 givenname: Karel surname: Koberna fullname: Koberna, Karel organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic – sequence: 8 givenname: Ronald surname: Berezney fullname: Berezney, Ronald organization: Department of Biological Sciences, State University of New York at Buffalo, Buffalo, New York 14260 – sequence: 9 givenname: Ivan surname: Ras̆ka fullname: Ras̆ka, Ivan organization: Department of Cell Biology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic and Institute of Cellular Biology and Pathology, 1st Faculty of Medicine, Charles University in Prague, Albertov 4, 128 00 Prague 2, Czech Republic |
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Snippet | Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a... Evidence is presented for the reversible, cold-dependent immunofluorescence detection of the epitope (hereafter referred to as epiC), recognized by a... Abstract Evidence is presented for the reversible, cold‐dependent immunofluorescence detection of the epitope (hereafter referred to as epiC ), recognized by a... |
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SubjectTerms | Actins - immunology anti-actin Blotting, Western cell cycle Cells, Cultured chromatin Chromatin - chemistry cold-dependent epitope detection DNA Replication G1 Phase Humans Image Processing, Computer-Assisted immunofluorescence microscopy Microscopy, Fluorescence nuclear actin S Phase |
Title | Replication-coupled modulation of early replicating chromatin domains detected by anti-actin antibody |
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