Arabidopsis replacement histone variant H3.3 occupies promoters of regulated genes
Histone variants establish structural and functional diversity of chromatin by affecting nucleosome stability and histone-protein interactions. H3.3 is an H3 histone variant that is incorporated into chromatin outside of S-phase in various eukaryotes. In animals, H3.3 is associated with active trans...
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description | Histone variants establish structural and functional diversity of chromatin by affecting nucleosome stability and histone-protein interactions. H3.3 is an H3 histone variant that is incorporated into chromatin outside of S-phase in various eukaryotes. In animals, H3.3 is associated with active transcription and possibly maintenance of transcriptional memory. Plant H3 variants, which evolved independently of their animal counterparts, are much less well understood.
We profile the H3.3 distribution in Arabidopsis at mono-nucleosomal resolution using native chromatin immunoprecipitation. This results in the precise mapping of H3.3-containing nucleosomes, which are not only enriched in gene bodies as previously reported, but also at a subset of promoter regions and downstream of the 3' ends of active genes. While H3.3 presence within transcribed regions is strongly associated with transcriptional activity, H3.3 at promoters is often independent of transcription. In particular, promoters with GA motifs carry H3.3 regardless of the gene expression levels. H3.3 on promoters of inactive genes is associated with H3K27me3 at gene bodies. In addition, H3.3-enriched plant promoters often contain RNA Pol II considerably upstream of the transcriptional start site. H3.3 and RNA Pol II are found on active as well as on inactive promoters and are enriched at strongly regulated genes.
In animals and plants, H3.3 organizes chromatin in transcribed regions and in promoters. The results suggest a function of H3.3 in transcriptional regulation and support a model that a single ancestral H3 evolved into H3 variants with similar sub-functionalization patterns in plants and animals. |
doi_str_mv | 10.1186/gb-2014-15-4-r62 |
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We profile the H3.3 distribution in Arabidopsis at mono-nucleosomal resolution using native chromatin immunoprecipitation. This results in the precise mapping of H3.3-containing nucleosomes, which are not only enriched in gene bodies as previously reported, but also at a subset of promoter regions and downstream of the 3' ends of active genes. While H3.3 presence within transcribed regions is strongly associated with transcriptional activity, H3.3 at promoters is often independent of transcription. In particular, promoters with GA motifs carry H3.3 regardless of the gene expression levels. H3.3 on promoters of inactive genes is associated with H3K27me3 at gene bodies. In addition, H3.3-enriched plant promoters often contain RNA Pol II considerably upstream of the transcriptional start site. H3.3 and RNA Pol II are found on active as well as on inactive promoters and are enriched at strongly regulated genes.
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We profile the H3.3 distribution in Arabidopsis at mono-nucleosomal resolution using native chromatin immunoprecipitation. This results in the precise mapping of H3.3-containing nucleosomes, which are not only enriched in gene bodies as previously reported, but also at a subset of promoter regions and downstream of the 3' ends of active genes. While H3.3 presence within transcribed regions is strongly associated with transcriptional activity, H3.3 at promoters is often independent of transcription. In particular, promoters with GA motifs carry H3.3 regardless of the gene expression levels. H3.3 on promoters of inactive genes is associated with H3K27me3 at gene bodies. In addition, H3.3-enriched plant promoters often contain RNA Pol II considerably upstream of the transcriptional start site. H3.3 and RNA Pol II are found on active as well as on inactive promoters and are enriched at strongly regulated genes.
In animals and plants, H3.3 organizes chromatin in transcribed regions and in promoters. The results suggest a function of H3.3 in transcriptional regulation and support a model that a single ancestral H3 evolved into H3 variants with similar sub-functionalization patterns in plants and animals.</description><subject>Arabidopsis</subject><subject>Arabidopsis - genetics</subject><subject>Biochemistry and Molecular Biology</subject><subject>Biokemi och molekylärbiologi</subject><subject>Developmental Biology</subject><subject>Evolutionary Biology</subject><subject>Evolutionsbiologi</subject><subject>Gene Expression Regulation, Plant</subject><subject>Genes, Plant</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Plant Biotechnology</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Binding</subject><subject>Utvecklingsbiologi</subject><subject>Växtbioteknologi</subject><issn>1465-6906</issn><issn>1474-760X</issn><issn>1474-7596</issn><issn>1474-760X</issn><issn>1465-6914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNks-L1TAQx4Mo7vr07kl69GDW_Oq0uQiPt-oKC4KoeAtpOu1G2qYm7Yr_vSlvFd9hwdMkmc9855tMCHnO2QXnNbzuGyoYV5SXVNEI4gE556pStAL27eG2hpKCZnBGnqT0nTGulYDH5EyoitW15ufk0z7axrdhTj4VEefBOhxxWoobn5YwYXFro7d5fyUvZBGcW2ePqZhjGMOCMRWhy2X9OtgF26LHCdNT8qizQ8Jnd3FHvrx7-_lwRa8_vv9w2F_TphRyodpKyUCXvBFtJ1vgDQjloLZK83wOHTjOHKJCBBStajfLVV3bjrdV7azcEXrUTT9xXhszRz_a-MsE600a1sbGLZiEBqAWKvOv7uUv_de9CbE362qEkDo73JE3RzyzI7YuP0q0w0nVaWbyN6YPt0axUkG19TscBRof7hE4zbgwmr4x20QNL40yeaJZ5eWdjRh-rJgWM_rkcBjshGFNGSxL4FoD_w9UaC2lYjqjL_693F9Tfz6G_A2nxb5K</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Shu, Huan</creator><creator>Nakamura, Miyuki</creator><creator>Siretskiy, Alexey</creator><creator>Borghi, Lorenzo</creator><creator>Moraes, Izabel</creator><creator>Wildhaber, Thomas</creator><creator>Gruissem, Wilhelm</creator><creator>Hennig, Lars</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>DF2</scope></search><sort><creationdate>20140101</creationdate><title>Arabidopsis replacement histone variant H3.3 occupies promoters of regulated genes</title><author>Shu, Huan ; Nakamura, Miyuki ; Siretskiy, Alexey ; Borghi, Lorenzo ; Moraes, Izabel ; Wildhaber, Thomas ; Gruissem, Wilhelm ; Hennig, Lars</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b523t-9a3306951b2df3d61b624c68a4910696f6c10cee4ee6e2d4d7088788af1d78ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Arabidopsis</topic><topic>Arabidopsis - genetics</topic><topic>Biochemistry and Molecular Biology</topic><topic>Biokemi och molekylärbiologi</topic><topic>Developmental Biology</topic><topic>Evolutionary Biology</topic><topic>Evolutionsbiologi</topic><topic>Gene Expression Regulation, Plant</topic><topic>Genes, Plant</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Plant Biotechnology</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Binding</topic><topic>Utvecklingsbiologi</topic><topic>Växtbioteknologi</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shu, Huan</creatorcontrib><creatorcontrib>Nakamura, Miyuki</creatorcontrib><creatorcontrib>Siretskiy, Alexey</creatorcontrib><creatorcontrib>Borghi, Lorenzo</creatorcontrib><creatorcontrib>Moraes, Izabel</creatorcontrib><creatorcontrib>Wildhaber, Thomas</creatorcontrib><creatorcontrib>Gruissem, Wilhelm</creatorcontrib><creatorcontrib>Hennig, Lars</creatorcontrib><creatorcontrib>Sveriges lantbruksuniversitet</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>Genome Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shu, Huan</au><au>Nakamura, Miyuki</au><au>Siretskiy, Alexey</au><au>Borghi, Lorenzo</au><au>Moraes, Izabel</au><au>Wildhaber, Thomas</au><au>Gruissem, Wilhelm</au><au>Hennig, Lars</au><aucorp>Sveriges lantbruksuniversitet</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arabidopsis replacement histone variant H3.3 occupies promoters of regulated genes</atitle><jtitle>Genome Biology</jtitle><addtitle>Genome Biol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>15</volume><issue>4</issue><spage>R62</spage><epage>R62</epage><pages>R62-R62</pages><issn>1465-6906</issn><issn>1474-760X</issn><issn>1474-7596</issn><eissn>1474-760X</eissn><eissn>1465-6914</eissn><abstract>Histone variants establish structural and functional diversity of chromatin by affecting nucleosome stability and histone-protein interactions. H3.3 is an H3 histone variant that is incorporated into chromatin outside of S-phase in various eukaryotes. In animals, H3.3 is associated with active transcription and possibly maintenance of transcriptional memory. Plant H3 variants, which evolved independently of their animal counterparts, are much less well understood.
We profile the H3.3 distribution in Arabidopsis at mono-nucleosomal resolution using native chromatin immunoprecipitation. This results in the precise mapping of H3.3-containing nucleosomes, which are not only enriched in gene bodies as previously reported, but also at a subset of promoter regions and downstream of the 3' ends of active genes. While H3.3 presence within transcribed regions is strongly associated with transcriptional activity, H3.3 at promoters is often independent of transcription. In particular, promoters with GA motifs carry H3.3 regardless of the gene expression levels. H3.3 on promoters of inactive genes is associated with H3K27me3 at gene bodies. In addition, H3.3-enriched plant promoters often contain RNA Pol II considerably upstream of the transcriptional start site. H3.3 and RNA Pol II are found on active as well as on inactive promoters and are enriched at strongly regulated genes.
In animals and plants, H3.3 organizes chromatin in transcribed regions and in promoters. The results suggest a function of H3.3 in transcriptional regulation and support a model that a single ancestral H3 evolved into H3 variants with similar sub-functionalization patterns in plants and animals.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24708891</pmid><doi>10.1186/gb-2014-15-4-r62</doi><oa>free_for_read</oa></addata></record> |
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subjects | Arabidopsis Arabidopsis - genetics Biochemistry and Molecular Biology Biokemi och molekylärbiologi Developmental Biology Evolutionary Biology Evolutionsbiologi Gene Expression Regulation, Plant Genes, Plant Histones - genetics Histones - metabolism Plant Biotechnology Plant Proteins - genetics Plant Proteins - metabolism Promoter Regions, Genetic Protein Binding Utvecklingsbiologi Växtbioteknologi |
title | Arabidopsis replacement histone variant H3.3 occupies promoters of regulated genes |
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