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Studies on ehrlich ascites tumour cells: DNA synthesis, and template activity of chromatin for DNA polymerase
Chromatin obtained from Ehrlich ascites cells on different days after cell inoculation has been assayed for its template activity with added DNA polymerase I. We have found that the template activity is 2 times higher in 7-8 day cell chromatin than in 4-day chromatin. Studies with added polylysine i...
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Published in: | Molecular and cellular biochemistry 1982-12, Vol.49 (3), p.169-175 |
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container_title | Molecular and cellular biochemistry |
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creator | Baghdjian, R B Itzhaki, S Ockey, C H Itzhaki, R F |
description | Chromatin obtained from Ehrlich ascites cells on different days after cell inoculation has been assayed for its template activity with added DNA polymerase I. We have found that the template activity is 2 times higher in 7-8 day cell chromatin than in 4-day chromatin. Studies with added polylysine indicate that this increase reflects an increase in initiation sites rather than in accessibility to the enzyme. We have measured the growth fraction, mitotic index and rate of DNA chain growth in the intact cells. The results show that there is a large decrease in growth fraction with age of tumour, the number of cells dropping out of cycle approximately doubling over the period studied. The overall rate of chain growth decreases in the later stages of growth but in a small proportion of cells there is an increase in rate with fewer replicons involved in DNA synthesis. We suggest that in the ascites cells there is a decrease in level of repair and replicative enzymes with age of tumour; this would account both for the increase in initiation sites in the chromatin DNA, for the decrease in number of cells in cycle and for the overall decreased rate of chain growth. |
doi_str_mv | 10.1007/BF00231179 |
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We have found that the template activity is 2 times higher in 7-8 day cell chromatin than in 4-day chromatin. Studies with added polylysine indicate that this increase reflects an increase in initiation sites rather than in accessibility to the enzyme. We have measured the growth fraction, mitotic index and rate of DNA chain growth in the intact cells. The results show that there is a large decrease in growth fraction with age of tumour, the number of cells dropping out of cycle approximately doubling over the period studied. The overall rate of chain growth decreases in the later stages of growth but in a small proportion of cells there is an increase in rate with fewer replicons involved in DNA synthesis. We suggest that in the ascites cells there is a decrease in level of repair and replicative enzymes with age of tumour; this would account both for the increase in initiation sites in the chromatin DNA, for the decrease in number of cells in cycle and for the overall decreased rate of chain growth.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1007/BF00231179</identifier><identifier>PMID: 7162507</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Animals ; Carcinoma, Ehrlich Tumor - metabolism ; Cell Nucleus - metabolism ; Chromatin - metabolism ; DNA Polymerase I - metabolism ; DNA Replication ; DNA, Neoplasm - biosynthesis ; DNA-Directed DNA Polymerase - metabolism ; Male ; Mice ; Mitosis - drug effects ; Polylysine - metabolism ; RNA, Neoplasm - metabolism ; Templates, Genetic</subject><ispartof>Molecular and cellular biochemistry, 1982-12, Vol.49 (3), p.169-175</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-25baf34cb87e4d80a18443a0dc5e0df808bb8760baffc2bef5d27c6931eecdd3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7162507$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baghdjian, R B</creatorcontrib><creatorcontrib>Itzhaki, S</creatorcontrib><creatorcontrib>Ockey, C H</creatorcontrib><creatorcontrib>Itzhaki, R F</creatorcontrib><title>Studies on ehrlich ascites tumour cells: DNA synthesis, and template activity of chromatin for DNA polymerase</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><description>Chromatin obtained from Ehrlich ascites cells on different days after cell inoculation has been assayed for its template activity with added DNA polymerase I. We have found that the template activity is 2 times higher in 7-8 day cell chromatin than in 4-day chromatin. Studies with added polylysine indicate that this increase reflects an increase in initiation sites rather than in accessibility to the enzyme. We have measured the growth fraction, mitotic index and rate of DNA chain growth in the intact cells. The results show that there is a large decrease in growth fraction with age of tumour, the number of cells dropping out of cycle approximately doubling over the period studied. The overall rate of chain growth decreases in the later stages of growth but in a small proportion of cells there is an increase in rate with fewer replicons involved in DNA synthesis. We suggest that in the ascites cells there is a decrease in level of repair and replicative enzymes with age of tumour; this would account both for the increase in initiation sites in the chromatin DNA, for the decrease in number of cells in cycle and for the overall decreased rate of chain growth.</description><subject>Animals</subject><subject>Carcinoma, Ehrlich Tumor - metabolism</subject><subject>Cell Nucleus - metabolism</subject><subject>Chromatin - metabolism</subject><subject>DNA Polymerase I - metabolism</subject><subject>DNA Replication</subject><subject>DNA, Neoplasm - biosynthesis</subject><subject>DNA-Directed DNA Polymerase - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mitosis - drug effects</subject><subject>Polylysine - metabolism</subject><subject>RNA, Neoplasm - metabolism</subject><subject>Templates, Genetic</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNpFkDFPwzAQRi0EKqWwsCN5YkAEzk5Su2ylUECqYKB75NgX1SiJi-0g5d-TQgXTSXfv-6R7hJwzuGEA4vZ-CcBTxsTsgIxZLtIkm7HZIRlDCpBIJsQxOQnhA2DAGRuRkWBTnoMYk-Y9dsZioK6luPG11RuqgrZxWMWucZ2nGus63NGH1zkNfRs3GGy4pqo1NGKzrVVEqnS0Xzb21FVUb7xrVLQtrZz_SW1d3TfoVcBTclSpOuDZfk7Ievm4Xjwnq7enl8V8lWgueUx4XqoqzXQpBWZGgmIyy1IFRucIppIgy-E0hYGqNC-xyg0XejpLGaI2Jp2Qy9_arXefHYZYNDbs3lAtui4UErgULOMDePULau9C8FgVW28b5fuCQbFTW_yrHeCLfWtXNmj-0L3L9BsDLnUp</recordid><startdate>19821210</startdate><enddate>19821210</enddate><creator>Baghdjian, R B</creator><creator>Itzhaki, S</creator><creator>Ockey, C H</creator><creator>Itzhaki, R F</creator><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>19821210</creationdate><title>Studies on ehrlich ascites tumour cells: DNA synthesis, and template activity of chromatin for DNA polymerase</title><author>Baghdjian, R B ; Itzhaki, S ; Ockey, C H ; Itzhaki, R F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-25baf34cb87e4d80a18443a0dc5e0df808bb8760baffc2bef5d27c6931eecdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Animals</topic><topic>Carcinoma, Ehrlich Tumor - metabolism</topic><topic>Cell Nucleus - metabolism</topic><topic>Chromatin - metabolism</topic><topic>DNA Polymerase I - metabolism</topic><topic>DNA Replication</topic><topic>DNA, Neoplasm - biosynthesis</topic><topic>DNA-Directed DNA Polymerase - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mitosis - drug effects</topic><topic>Polylysine - metabolism</topic><topic>RNA, Neoplasm - metabolism</topic><topic>Templates, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baghdjian, R B</creatorcontrib><creatorcontrib>Itzhaki, S</creatorcontrib><creatorcontrib>Ockey, C H</creatorcontrib><creatorcontrib>Itzhaki, R F</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>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baghdjian, R B</au><au>Itzhaki, S</au><au>Ockey, C H</au><au>Itzhaki, R F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on ehrlich ascites tumour cells: DNA synthesis, and template activity of chromatin for DNA polymerase</atitle><jtitle>Molecular and cellular biochemistry</jtitle><addtitle>Mol Cell Biochem</addtitle><date>1982-12-10</date><risdate>1982</risdate><volume>49</volume><issue>3</issue><spage>169</spage><epage>175</epage><pages>169-175</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>Chromatin obtained from Ehrlich ascites cells on different days after cell inoculation has been assayed for its template activity with added DNA polymerase I. We have found that the template activity is 2 times higher in 7-8 day cell chromatin than in 4-day chromatin. Studies with added polylysine indicate that this increase reflects an increase in initiation sites rather than in accessibility to the enzyme. We have measured the growth fraction, mitotic index and rate of DNA chain growth in the intact cells. The results show that there is a large decrease in growth fraction with age of tumour, the number of cells dropping out of cycle approximately doubling over the period studied. The overall rate of chain growth decreases in the later stages of growth but in a small proportion of cells there is an increase in rate with fewer replicons involved in DNA synthesis. We suggest that in the ascites cells there is a decrease in level of repair and replicative enzymes with age of tumour; this would account both for the increase in initiation sites in the chromatin DNA, for the decrease in number of cells in cycle and for the overall decreased rate of chain growth.</abstract><cop>Netherlands</cop><pmid>7162507</pmid><doi>10.1007/BF00231179</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Carcinoma, Ehrlich Tumor - metabolism Cell Nucleus - metabolism Chromatin - metabolism DNA Polymerase I - metabolism DNA Replication DNA, Neoplasm - biosynthesis DNA-Directed DNA Polymerase - metabolism Male Mice Mitosis - drug effects Polylysine - metabolism RNA, Neoplasm - metabolism Templates, Genetic |
title | Studies on ehrlich ascites tumour cells: DNA synthesis, and template activity of chromatin for DNA polymerase |
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