Selective Requirements for Histone H3 and H4 N Termini in p300-Dependent Transcriptional Activation from Chromatin
The N-terminal tails of the core histones play important roles in transcriptional regulation, but their mechanism(s) of action are poorly understood. Here, pure chromatin templates assembled with varied combinations of recombinant wild-type and mutant core histones have been employed to ascertain th...
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Veröffentlicht in: | Molecular cell 2002-04, Vol.9 (4), p.811-821 |
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creator | An, Woojin Palhan, Vikas B Karymov, Mikhail A Leuba, Sanford H Roeder, Robert G |
description | The N-terminal tails of the core histones play important roles in transcriptional regulation, but their mechanism(s) of action are poorly understood. Here, pure chromatin templates assembled with varied combinations of recombinant wild-type and mutant core histones have been employed to ascertain the role of individual histone tails, both in overall acetylation patterns and in transcription. In vitro assays show an indispensable role for H3 and H4 tails, especially major lysine substrates, in p300-dependent transcriptional activation, as well as activator-targeted acetylation of promoter-proximal histone tails by p300. These results indicate, first, that constraints to transcription are imposed by nucleosomal histone components other than histone N-terminal tails and, second, that the histone N-terminal tails have selective roles, which can be modulated by targeted acetylation, in transcriptional activation by p300. |
doi_str_mv | 10.1016/S1097-2765(02)00497-5 |
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Here, pure chromatin templates assembled with varied combinations of recombinant wild-type and mutant core histones have been employed to ascertain the role of individual histone tails, both in overall acetylation patterns and in transcription. In vitro assays show an indispensable role for H3 and H4 tails, especially major lysine substrates, in p300-dependent transcriptional activation, as well as activator-targeted acetylation of promoter-proximal histone tails by p300. 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These results indicate, first, that constraints to transcription are imposed by nucleosomal histone components other than histone N-terminal tails and, second, that the histone N-terminal tails have selective roles, which can be modulated by targeted acetylation, in transcriptional activation by p300.</description><subject>Acetylation</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Chromatin - genetics</subject><subject>Histones - chemistry</subject><subject>Histones - genetics</subject><subject>Histones - physiology</subject><subject>Models, Genetic</subject><subject>Molecular Sequence Data</subject><subject>Nuclear Proteins - physiology</subject><subject>Nucleosomes - metabolism</subject><subject>p300 protein</subject><subject>Precipitin Tests</subject><subject>Protein Processing, Post-Translational</subject><subject>Protein Structure, Tertiary</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - physiology</subject><subject>Structure-Activity Relationship</subject><subject>Templates, Genetic</subject><subject>Trans-Activators - physiology</subject><subject>Transcriptional Activation - physiology</subject><subject>Xenopus laevis - genetics</subject><subject>Xenopus laevis - metabolism</subject><issn>1097-2765</issn><issn>1097-4164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaNK0P6FFp5IenIw-LFmnErYfWwgtNNuzkOURVbFlR_IG-u9j7y70mMtoXvHMvDAvIe8YXDNg6uaegdEV16q-Av4RQC6qfkEuDt-SKfny1K_IOXldyl8AJuvGvCLnjJlGMM0vSL7HHv0cH5H-wod9zDhgmgsNY6bbWOYxId0K6lJHt5L-oDvMQ0yRxkQnAVB9xglTt4zQXXap-BynOY7J9fR23epWQUMeB7r5s9RFpzfkLLi-4NvTe0l-f_2y22yru5_fvm9u7yovOdSVc5xjxxVyHRCc8kFqzdsQguIKjOFGtT4Y07TGB9ZxoZG3TXCylY1sRScuyYfj3imPD3sssx1i8dj3LuG4L1YzJYxU9bMga4SoAfQC1kfQ57GUjMFOOQ4u_7MM7JqKPaRi15Nb4PaQil0N3p8M9u2A3f-pUwwL8OkI4HKPx4jZFh8xeeyWQPxsuzE-Y_EEfuicpQ</recordid><startdate>200204</startdate><enddate>200204</enddate><creator>An, Woojin</creator><creator>Palhan, Vikas B</creator><creator>Karymov, Mikhail A</creator><creator>Leuba, Sanford H</creator><creator>Roeder, Robert G</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>200204</creationdate><title>Selective Requirements for Histone H3 and H4 N Termini in p300-Dependent Transcriptional Activation from Chromatin</title><author>An, Woojin ; Palhan, Vikas B ; Karymov, Mikhail A ; Leuba, Sanford H ; Roeder, Robert G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4205-aa22ed26e27fe0a6cf4772bfff626099296bcf998b9cf1d237e2b8fa4b484b3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Acetylation</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Chromatin - genetics</topic><topic>Histones - chemistry</topic><topic>Histones - genetics</topic><topic>Histones - physiology</topic><topic>Models, Genetic</topic><topic>Molecular Sequence Data</topic><topic>Nuclear Proteins - physiology</topic><topic>Nucleosomes - metabolism</topic><topic>p300 protein</topic><topic>Precipitin Tests</topic><topic>Protein Processing, Post-Translational</topic><topic>Protein Structure, Tertiary</topic><topic>Recombinant Fusion Proteins - chemistry</topic><topic>Recombinant Fusion Proteins - physiology</topic><topic>Structure-Activity Relationship</topic><topic>Templates, Genetic</topic><topic>Trans-Activators - physiology</topic><topic>Transcriptional Activation - physiology</topic><topic>Xenopus laevis - genetics</topic><topic>Xenopus laevis - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>An, Woojin</creatorcontrib><creatorcontrib>Palhan, Vikas B</creatorcontrib><creatorcontrib>Karymov, Mikhail A</creatorcontrib><creatorcontrib>Leuba, Sanford H</creatorcontrib><creatorcontrib>Roeder, Robert G</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>MEDLINE - Academic</collection><jtitle>Molecular cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>An, Woojin</au><au>Palhan, Vikas B</au><au>Karymov, Mikhail A</au><au>Leuba, Sanford H</au><au>Roeder, Robert G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective Requirements for Histone H3 and H4 N Termini in p300-Dependent Transcriptional Activation from Chromatin</atitle><jtitle>Molecular cell</jtitle><addtitle>Mol Cell</addtitle><date>2002-04</date><risdate>2002</risdate><volume>9</volume><issue>4</issue><spage>811</spage><epage>821</epage><pages>811-821</pages><issn>1097-2765</issn><eissn>1097-4164</eissn><abstract>The N-terminal tails of the core histones play important roles in transcriptional regulation, but their mechanism(s) of action are poorly understood. Here, pure chromatin templates assembled with varied combinations of recombinant wild-type and mutant core histones have been employed to ascertain the role of individual histone tails, both in overall acetylation patterns and in transcription. In vitro assays show an indispensable role for H3 and H4 tails, especially major lysine substrates, in p300-dependent transcriptional activation, as well as activator-targeted acetylation of promoter-proximal histone tails by p300. These results indicate, first, that constraints to transcription are imposed by nucleosomal histone components other than histone N-terminal tails and, second, that the histone N-terminal tails have selective roles, which can be modulated by targeted acetylation, in transcriptional activation by p300.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11983172</pmid><doi>10.1016/S1097-2765(02)00497-5</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylation Amino Acid Sequence Animals Chromatin - genetics Histones - chemistry Histones - genetics Histones - physiology Models, Genetic Molecular Sequence Data Nuclear Proteins - physiology Nucleosomes - metabolism p300 protein Precipitin Tests Protein Processing, Post-Translational Protein Structure, Tertiary Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - physiology Structure-Activity Relationship Templates, Genetic Trans-Activators - physiology Transcriptional Activation - physiology Xenopus laevis - genetics Xenopus laevis - metabolism |
title | Selective Requirements for Histone H3 and H4 N Termini in p300-Dependent Transcriptional Activation from Chromatin |
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