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The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase
Eukaryotic messenger RNA precursors (pre-mRNAs) synthesized by RNA polymerase II (RNAP II) are processed co-transcriptionally. The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II is thought to mediate the coupling of transcription with pre-mRNA processing by coordinating t...
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Published in: | The Journal of biological chemistry 2009-03, Vol.284 (13), p.8692-8702 |
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creator | Natalizio, Barbara J. Robson-Dixon, Nicole D. Garcia-Blanco, Mariano A. |
description | Eukaryotic messenger RNA precursors (pre-mRNAs) synthesized by RNA polymerase II (RNAP II) are processed co-transcriptionally. The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II is thought to mediate the coupling of transcription with pre-mRNA processing by coordinating the recruitment of processing factors during synthesis of nascent transcripts. Previous studies have demonstrated that the phosphorylated CTD is required for efficient co-transcriptional processing. In the study presented here we investigated whether the CTD is sufficient to coordinate transcription with pre-mRNA capping and splicing in the context of two other DNA-dependent RNA polymerases, mammalian RNAP III and bacteriophage T7 RNAP. Our results indicate that the CTD fused to the largest subunit of RNAP III (POLR3A) is not sufficient to enhance co-transcriptional pre-mRNA splicing or capping in vivo. Additionally, we analyzed a T7 RNAP-CTD fusion protein and examined its ability to enhance pre-mRNA splicing and capping of both constitutively and alternatively spliced substrates. We observed that the CTD in the context of T7 RNAP was not sufficient to enhance pre-mRNA splicing or capping either in vitro or in vivo. We propose that the efficient coupling of transcription to pre-mRNA processing requires not only the phosphorylated CTD but also other RNAP II specific subunits or associated factors. |
doi_str_mv | 10.1074/jbc.M806919200 |
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The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II is thought to mediate the coupling of transcription with pre-mRNA processing by coordinating the recruitment of processing factors during synthesis of nascent transcripts. Previous studies have demonstrated that the phosphorylated CTD is required for efficient co-transcriptional processing. In the study presented here we investigated whether the CTD is sufficient to coordinate transcription with pre-mRNA capping and splicing in the context of two other DNA-dependent RNA polymerases, mammalian RNAP III and bacteriophage T7 RNAP. Our results indicate that the CTD fused to the largest subunit of RNAP III (POLR3A) is not sufficient to enhance co-transcriptional pre-mRNA splicing or capping in vivo. Additionally, we analyzed a T7 RNAP-CTD fusion protein and examined its ability to enhance pre-mRNA splicing and capping of both constitutively and alternatively spliced substrates. We observed that the CTD in the context of T7 RNAP was not sufficient to enhance pre-mRNA splicing or capping either in vitro or in vivo. 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The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II is thought to mediate the coupling of transcription with pre-mRNA processing by coordinating the recruitment of processing factors during synthesis of nascent transcripts. Previous studies have demonstrated that the phosphorylated CTD is required for efficient co-transcriptional processing. In the study presented here we investigated whether the CTD is sufficient to coordinate transcription with pre-mRNA capping and splicing in the context of two other DNA-dependent RNA polymerases, mammalian RNAP III and bacteriophage T7 RNAP. Our results indicate that the CTD fused to the largest subunit of RNAP III (POLR3A) is not sufficient to enhance co-transcriptional pre-mRNA splicing or capping in vivo. Additionally, we analyzed a T7 RNAP-CTD fusion protein and examined its ability to enhance pre-mRNA splicing and capping of both constitutively and alternatively spliced substrates. We observed that the CTD in the context of T7 RNAP was not sufficient to enhance pre-mRNA splicing or capping either in vitro or in vivo. We propose that the efficient coupling of transcription to pre-mRNA processing requires not only the phosphorylated CTD but also other RNAP II specific subunits or associated factors.</description><subject>Cell Line</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Humans</subject><subject>Protein Structure, Tertiary - physiology</subject><subject>RNA Caps - genetics</subject><subject>RNA Caps - metabolism</subject><subject>RNA Polymerase II - genetics</subject><subject>RNA Polymerase II - metabolism</subject><subject>RNA Polymerase III - genetics</subject><subject>RNA Polymerase III - metabolism</subject><subject>RNA Splicing - physiology</subject><subject>RNA: Processing and Catalysis</subject><subject>Transcription, Genetic - physiology</subject><subject>Viral Proteins - genetics</subject><subject>Viral Proteins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkk1v1DAQhiMEokvhyhEsIXHLYjtf9gWpShdYqZSKbSVuluOMN66SOLWzpfuH-J04ZMXCAeGLLc0z78z4nSh6SfCS4CJ9d1up5WeGc044xfhRtCCYJXGSkW-PowXGlMScZuwkeub9LQ4n5eRpdEI4KfKMFovox3UDqJSusg_7Nh7BdaaXLTq3nTQ9shp9vTxDV7bdd-CkB7Reo7VHl3ZEm53WRhnoRzRatOob2StAY5BbHQJqPwlcOYi7SaWUw2D6LbIObYY2EOEdakwZpe1HeBgnXKJzozW4SfdY93n0RMvWw4vDfRrdfFhdl5_iiy8f1-XZRawyiscYQIOktNBaAtAKM0l0UnDAOeQ6DUGW8KzWCVEadPg0xmldZFolKdGaAk9Oo_ez7rCrOqhV6MLJVgzOdNLthZVG_B3pTSO29l7QPOOUsiDw9iDg7N0O_Cg64xW0rezB7rzIC5xhnGT_BWkwEud5EcDlDCpnvXegf3dDsJh2QIQdEMcdCAmv_pzhiB9MD8CbGWjMtvluHIjKWNVAJyhLBUkEyzkN1OuZ0tIKuXXGi5sNxSTBJMeMFNOsbCYgOHJvwAn_y3aog6YaRW3Nv3r8CS8i18M</recordid><startdate>20090327</startdate><enddate>20090327</enddate><creator>Natalizio, Barbara J.</creator><creator>Robson-Dixon, Nicole D.</creator><creator>Garcia-Blanco, Mariano A.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</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>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090327</creationdate><title>The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase</title><author>Natalizio, Barbara J. ; Robson-Dixon, Nicole D. ; Garcia-Blanco, Mariano A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-eefea227ffaee2b08a1f379e06e6f4efe8395df31cfef069892d75fc341ff2e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Cell Line</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Humans</topic><topic>Protein Structure, Tertiary - physiology</topic><topic>RNA Caps - genetics</topic><topic>RNA Caps - metabolism</topic><topic>RNA Polymerase II - genetics</topic><topic>RNA Polymerase II - metabolism</topic><topic>RNA Polymerase III - genetics</topic><topic>RNA Polymerase III - metabolism</topic><topic>RNA Splicing - physiology</topic><topic>RNA: Processing and Catalysis</topic><topic>Transcription, Genetic - physiology</topic><topic>Viral Proteins - genetics</topic><topic>Viral Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Natalizio, Barbara J.</creatorcontrib><creatorcontrib>Robson-Dixon, Nicole D.</creatorcontrib><creatorcontrib>Garcia-Blanco, Mariano A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Natalizio, Barbara J.</au><au>Robson-Dixon, Nicole D.</au><au>Garcia-Blanco, Mariano A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2009-03-27</date><risdate>2009</risdate><volume>284</volume><issue>13</issue><spage>8692</spage><epage>8702</epage><pages>8692-8702</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Eukaryotic messenger RNA precursors (pre-mRNAs) synthesized by RNA polymerase II (RNAP II) are processed co-transcriptionally. The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II is thought to mediate the coupling of transcription with pre-mRNA processing by coordinating the recruitment of processing factors during synthesis of nascent transcripts. Previous studies have demonstrated that the phosphorylated CTD is required for efficient co-transcriptional processing. In the study presented here we investigated whether the CTD is sufficient to coordinate transcription with pre-mRNA capping and splicing in the context of two other DNA-dependent RNA polymerases, mammalian RNAP III and bacteriophage T7 RNAP. Our results indicate that the CTD fused to the largest subunit of RNAP III (POLR3A) is not sufficient to enhance co-transcriptional pre-mRNA splicing or capping in vivo. Additionally, we analyzed a T7 RNAP-CTD fusion protein and examined its ability to enhance pre-mRNA splicing and capping of both constitutively and alternatively spliced substrates. We observed that the CTD in the context of T7 RNAP was not sufficient to enhance pre-mRNA splicing or capping either in vitro or in vivo. We propose that the efficient coupling of transcription to pre-mRNA processing requires not only the phosphorylated CTD but also other RNAP II specific subunits or associated factors.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19176527</pmid><doi>10.1074/jbc.M806919200</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Line DNA-Directed RNA Polymerases - genetics DNA-Directed RNA Polymerases - metabolism Humans Protein Structure, Tertiary - physiology RNA Caps - genetics RNA Caps - metabolism RNA Polymerase II - genetics RNA Polymerase II - metabolism RNA Polymerase III - genetics RNA Polymerase III - metabolism RNA Splicing - physiology RNA: Processing and Catalysis Transcription, Genetic - physiology Viral Proteins - genetics Viral Proteins - metabolism |
title | The Carboxyl-terminal Domain of RNA Polymerase II Is Not Sufficient to Enhance the Efficiency of Pre-mRNA Capping or Splicing in the Context of a Different Polymerase |
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