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Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei
Using HeLa cells, we have developed methods to determine 1) the number of RNA polymerases that are active at any moment, 2) the number of transcription sites, and 3) the number of polymerases associated with one transcription unit. To count engaged polymerases, cells were encapsulated in agarose, pe...
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Published in: | Molecular biology of the cell 1998-06, Vol.9 (6), p.1523-1536 |
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container_title | Molecular biology of the cell |
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creator | Jackson, D A Iborra, F J Manders, E M Cook, P R |
description | Using HeLa cells, we have developed methods to determine 1) the number of RNA polymerases that are active at any moment, 2) the number of transcription sites, and 3) the number of polymerases associated with one transcription unit. To count engaged polymerases, cells were encapsulated in agarose, permeabilized, treated with ribonuclease, and the now-truncated transcripts extended in [32P]uridine triphosphate; then, the number of growing transcripts was calculated from the total number of nucleotides incorporated and the average increment in length of the transcripts. Approximately 15, 000 transcripts were elongated by polymerase I, and approximately 75,000 were elongated by polymerases II and III. Transcription sites were detected after the cells were grown in bromouridine for |
doi_str_mv | 10.1091/mbc.9.6.1523 |
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To count engaged polymerases, cells were encapsulated in agarose, permeabilized, treated with ribonuclease, and the now-truncated transcripts extended in [32P]uridine triphosphate; then, the number of growing transcripts was calculated from the total number of nucleotides incorporated and the average increment in length of the transcripts. Approximately 15, 000 transcripts were elongated by polymerase I, and approximately 75,000 were elongated by polymerases II and III. Transcription sites were detected after the cells were grown in bromouridine for <2.5 min, after which the resulting bromo-RNA was labeled with gold particles; electron microscopy showed that most extranucleolar transcripts were concentrated in approximately 2400 sites with diameters of approximately 80 nm. The number of polymerases associated with a transcription unit was counted after templates were spread over a large area; most extranucleolar units were associated with one elongating complex. These results suggest that many templates are attached in a "cloud" of loops around a site; each site, or transcription "factory," would contain approximately 30 active polymerases and associated transcripts.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.9.6.1523</identifier><identifier>PMID: 9614191</identifier><language>eng</language><publisher>United States: The American Society for Cell Biology</publisher><subject>Cell Nucleolus ; Cell Nucleus ; Cytidine Triphosphate - metabolism ; DNA-Directed RNA Polymerases - metabolism ; Enzyme Activation ; HeLa Cells ; Humans ; RNA Polymerase I - metabolism ; RNA Polymerase II - metabolism ; Transcription, Genetic ; Uridine - analogs & derivatives</subject><ispartof>Molecular biology of the cell, 1998-06, Vol.9 (6), p.1523-1536</ispartof><rights>Copyright © 1998, The American Society for Cell Biology 1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-daf5a9ae4577b290550f59c1976603df17201a71986fdd82516c9bad185385393</citedby><cites>FETCH-LOGICAL-c442t-daf5a9ae4577b290550f59c1976603df17201a71986fdd82516c9bad185385393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC25378/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC25378/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9614191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jackson, D A</creatorcontrib><creatorcontrib>Iborra, F J</creatorcontrib><creatorcontrib>Manders, E M</creatorcontrib><creatorcontrib>Cook, P R</creatorcontrib><title>Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>Using HeLa cells, we have developed methods to determine 1) the number of RNA polymerases that are active at any moment, 2) the number of transcription sites, and 3) the number of polymerases associated with one transcription unit. To count engaged polymerases, cells were encapsulated in agarose, permeabilized, treated with ribonuclease, and the now-truncated transcripts extended in [32P]uridine triphosphate; then, the number of growing transcripts was calculated from the total number of nucleotides incorporated and the average increment in length of the transcripts. Approximately 15, 000 transcripts were elongated by polymerase I, and approximately 75,000 were elongated by polymerases II and III. Transcription sites were detected after the cells were grown in bromouridine for <2.5 min, after which the resulting bromo-RNA was labeled with gold particles; electron microscopy showed that most extranucleolar transcripts were concentrated in approximately 2400 sites with diameters of approximately 80 nm. The number of polymerases associated with a transcription unit was counted after templates were spread over a large area; most extranucleolar units were associated with one elongating complex. These results suggest that many templates are attached in a "cloud" of loops around a site; each site, or transcription "factory," would contain approximately 30 active polymerases and associated transcripts.</description><subject>Cell Nucleolus</subject><subject>Cell Nucleus</subject><subject>Cytidine Triphosphate - metabolism</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Enzyme Activation</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>RNA Polymerase I - metabolism</subject><subject>RNA Polymerase II - metabolism</subject><subject>Transcription, Genetic</subject><subject>Uridine - analogs & derivatives</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpVkFFLwzAQx4Moc07ffBXyAdaaa5u0AV_GUCeMCaLPIU3TLdKmJWmF-elt2ZgKB3f87353xx-hWyAhEA73da5CHrIQaBSfoSnwmAcJzdj5UBPKg0FPLtGV95-EQJKwdIImnEECHKZot-nrXDuPpS1w47bSmm_ZmcbipsRvmwVum2pfaye99nNspVfadrhz0nrlTNsN4kj-CiPaW9N5bCxe6bXEtleVNtfoopSV1zfHPEMfT4_vy1Wwfn1-WS7WgUqSqAsKWVLJpU5omuYRJ5SSknIFPGWMxEUJaURApsAzVhZFFlFgiueygIzGQ_B4hh4Oe9s-r3UxvutkJVpnaun2opFG_O9YsxPb5ktENE6zAZ8fcOUa750uTyQQMdotBrsFF0yMdg_jd3-vnYaP_sY_Flx90w</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Jackson, D A</creator><creator>Iborra, F J</creator><creator>Manders, E M</creator><creator>Cook, P R</creator><general>The American Society for Cell Biology</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>5PM</scope></search><sort><creationdate>19980601</creationdate><title>Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei</title><author>Jackson, D A ; Iborra, F J ; Manders, E M ; Cook, P R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-daf5a9ae4577b290550f59c1976603df17201a71986fdd82516c9bad185385393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Cell Nucleolus</topic><topic>Cell Nucleus</topic><topic>Cytidine Triphosphate - metabolism</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Enzyme Activation</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>RNA Polymerase I - metabolism</topic><topic>RNA Polymerase II - metabolism</topic><topic>Transcription, Genetic</topic><topic>Uridine - analogs & derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jackson, D A</creatorcontrib><creatorcontrib>Iborra, F J</creatorcontrib><creatorcontrib>Manders, E M</creatorcontrib><creatorcontrib>Cook, P R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jackson, D A</au><au>Iborra, F J</au><au>Manders, E M</au><au>Cook, P R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>9</volume><issue>6</issue><spage>1523</spage><epage>1536</epage><pages>1523-1536</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>Using HeLa cells, we have developed methods to determine 1) the number of RNA polymerases that are active at any moment, 2) the number of transcription sites, and 3) the number of polymerases associated with one transcription unit. To count engaged polymerases, cells were encapsulated in agarose, permeabilized, treated with ribonuclease, and the now-truncated transcripts extended in [32P]uridine triphosphate; then, the number of growing transcripts was calculated from the total number of nucleotides incorporated and the average increment in length of the transcripts. Approximately 15, 000 transcripts were elongated by polymerase I, and approximately 75,000 were elongated by polymerases II and III. Transcription sites were detected after the cells were grown in bromouridine for <2.5 min, after which the resulting bromo-RNA was labeled with gold particles; electron microscopy showed that most extranucleolar transcripts were concentrated in approximately 2400 sites with diameters of approximately 80 nm. The number of polymerases associated with a transcription unit was counted after templates were spread over a large area; most extranucleolar units were associated with one elongating complex. These results suggest that many templates are attached in a "cloud" of loops around a site; each site, or transcription "factory," would contain approximately 30 active polymerases and associated transcripts.</abstract><cop>United States</cop><pub>The American Society for Cell Biology</pub><pmid>9614191</pmid><doi>10.1091/mbc.9.6.1523</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | PubMed Central |
subjects | Cell Nucleolus Cell Nucleus Cytidine Triphosphate - metabolism DNA-Directed RNA Polymerases - metabolism Enzyme Activation HeLa Cells Humans RNA Polymerase I - metabolism RNA Polymerase II - metabolism Transcription, Genetic Uridine - analogs & derivatives |
title | Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei |
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