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Distinct and concurrent pathways of Pol II‐ and Pol IV‐dependent siRNA biogenesis at a repetitive trans‐silencer locus in Arabidopsis thaliana
Short interfering RNAs (siRNAs) homologous to transcriptional regulatory regions can induce RNA‐directed DNA methylation (RdDM) and transcriptional gene silencing (TGS) of target genes. In our system, siRNAs are produced by transcribing an inverted DNA repeat (IR) of enhancer sequences, yielding a h...
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Published in: | The Plant journal : for cell and molecular biology 2014-07, Vol.79 (1), p.127-138 |
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creator | Sasaki, Taku Lee, Tzuu‐fen Liao, Wen‐Wei Naumann, Ulf Liao, Jo‐Ling Eun, Changho Huang, Ya‐Yi Fu, Jason L Chen, Pao‐Yang Meyers, Blake C Matzke, Antonius J.M Matzke, Marjori |
description | Short interfering RNAs (siRNAs) homologous to transcriptional regulatory regions can induce RNA‐directed DNA methylation (RdDM) and transcriptional gene silencing (TGS) of target genes. In our system, siRNAs are produced by transcribing an inverted DNA repeat (IR) of enhancer sequences, yielding a hairpin RNA that is processed by several Dicer activities into siRNAs of 21–24 nt. Primarily 24‐nt siRNAs trigger RdDM of the target enhancer in trans and TGS of a downstream GFP reporter gene. We analyzed siRNA accumulation from two different structural forms of a trans‐silencer locus in which tandem repeats are embedded in the enhancer IR and distinguished distinct RNA polymerase II (Pol II)‐ and Pol IV‐dependent pathways of siRNA biogenesis. At the original silencer locus, Pol‐II transcription of the IR from a 35S promoter produces a hairpin RNA that is diced into abundant siRNAs of 21–24 nt. A silencer variant lacking the 35S promoter revealed a normally masked Pol IV‐dependent pathway that produces low levels of 24‐nt siRNAs from the tandem repeats. Both pathways operate concurrently at the original silencer locus. siRNAs accrue only from specific regions of the enhancer and embedded tandem repeat. Analysis of these sequences and endogenous tandem repeats producing siRNAs revealed the preferential accumulation of siRNAs at GC‐rich regions containing methylated CG dinucleotides. In addition to supporting a correlation between base composition, DNA methylation and siRNA accumulation, our results highlight the complexity of siRNA biogenesis at repetitive loci and show that Pol II and Pol IV use different promoters to transcribe the same template. |
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In our system, siRNAs are produced by transcribing an inverted DNA repeat (IR) of enhancer sequences, yielding a hairpin RNA that is processed by several Dicer activities into siRNAs of 21–24 nt. Primarily 24‐nt siRNAs trigger RdDM of the target enhancer in trans and TGS of a downstream GFP reporter gene. We analyzed siRNA accumulation from two different structural forms of a trans‐silencer locus in which tandem repeats are embedded in the enhancer IR and distinguished distinct RNA polymerase II (Pol II)‐ and Pol IV‐dependent pathways of siRNA biogenesis. At the original silencer locus, Pol‐II transcription of the IR from a 35S promoter produces a hairpin RNA that is diced into abundant siRNAs of 21–24 nt. A silencer variant lacking the 35S promoter revealed a normally masked Pol IV‐dependent pathway that produces low levels of 24‐nt siRNAs from the tandem repeats. Both pathways operate concurrently at the original silencer locus. siRNAs accrue only from specific regions of the enhancer and embedded tandem repeat. Analysis of these sequences and endogenous tandem repeats producing siRNAs revealed the preferential accumulation of siRNAs at GC‐rich regions containing methylated CG dinucleotides. In addition to supporting a correlation between base composition, DNA methylation and siRNA accumulation, our results highlight the complexity of siRNA biogenesis at repetitive loci and show that Pol II and Pol IV use different promoters to transcribe the same template.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.12545</identifier><identifier>PMID: 24798377</identifier><language>eng</language><publisher>England: Blackwell Science</publisher><subject>Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Base Sequence ; Biosynthesis ; Botany ; DNA Methylation ; DNA-directed RNA polymerase ; DNA-Directed RNA Polymerases - genetics ; DNA-Directed RNA Polymerases - metabolism ; enhancer elements ; Gene Expression Regulation, Plant ; Gene Silencing ; Genes, Reporter ; High-Throughput Nucleotide Sequencing ; inverted repeats ; loci ; Meristem - genetics ; Meristem - metabolism ; Models, Biological ; Molecular Sequence Data ; Mutation ; Plant Shoots - genetics ; Plant Shoots - metabolism ; Plants, Genetically Modified ; Pol IV ; Promoter Regions, Genetic - genetics ; reporter genes ; Ribonucleic acid ; RNA ; RNA Polymerase II - genetics ; RNA Polymerase II - metabolism ; RNA polymerase II ; RNA, Plant - genetics ; RNA, Plant - metabolism ; RNA, Small Interfering - genetics ; RNA, Small Interfering - metabolism ; RNA‐directed DNA methylation ; Sequence Analysis ; siRNAs ; small interfering RNA ; tandem repeat sequences ; Tandem Repeat Sequences - genetics ; tandem repeats ; transcription (genetics)</subject><ispartof>The Plant journal : for cell and molecular biology, 2014-07, Vol.79 (1), p.127-138</ispartof><rights>2014 The Authors The Plant Journal © 2014 John Wiley & Sons Ltd</rights><rights>2014 The Authors The Plant Journal © 2014 John Wiley & Sons Ltd.</rights><rights>Copyright © 2014 John Wiley & Sons Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24798377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sasaki, Taku</creatorcontrib><creatorcontrib>Lee, Tzuu‐fen</creatorcontrib><creatorcontrib>Liao, Wen‐Wei</creatorcontrib><creatorcontrib>Naumann, Ulf</creatorcontrib><creatorcontrib>Liao, Jo‐Ling</creatorcontrib><creatorcontrib>Eun, Changho</creatorcontrib><creatorcontrib>Huang, Ya‐Yi</creatorcontrib><creatorcontrib>Fu, Jason L</creatorcontrib><creatorcontrib>Chen, Pao‐Yang</creatorcontrib><creatorcontrib>Meyers, Blake C</creatorcontrib><creatorcontrib>Matzke, Antonius J.M</creatorcontrib><creatorcontrib>Matzke, Marjori</creatorcontrib><title>Distinct and concurrent pathways of Pol II‐ and Pol IV‐dependent siRNA biogenesis at a repetitive trans‐silencer locus in Arabidopsis thaliana</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Short interfering RNAs (siRNAs) homologous to transcriptional regulatory regions can induce RNA‐directed DNA methylation (RdDM) and transcriptional gene silencing (TGS) of target genes. In our system, siRNAs are produced by transcribing an inverted DNA repeat (IR) of enhancer sequences, yielding a hairpin RNA that is processed by several Dicer activities into siRNAs of 21–24 nt. Primarily 24‐nt siRNAs trigger RdDM of the target enhancer in trans and TGS of a downstream GFP reporter gene. We analyzed siRNA accumulation from two different structural forms of a trans‐silencer locus in which tandem repeats are embedded in the enhancer IR and distinguished distinct RNA polymerase II (Pol II)‐ and Pol IV‐dependent pathways of siRNA biogenesis. At the original silencer locus, Pol‐II transcription of the IR from a 35S promoter produces a hairpin RNA that is diced into abundant siRNAs of 21–24 nt. A silencer variant lacking the 35S promoter revealed a normally masked Pol IV‐dependent pathway that produces low levels of 24‐nt siRNAs from the tandem repeats. Both pathways operate concurrently at the original silencer locus. siRNAs accrue only from specific regions of the enhancer and embedded tandem repeat. Analysis of these sequences and endogenous tandem repeats producing siRNAs revealed the preferential accumulation of siRNAs at GC‐rich regions containing methylated CG dinucleotides. In addition to supporting a correlation between base composition, DNA methylation and siRNA accumulation, our results highlight the complexity of siRNA biogenesis at repetitive loci and show that Pol II and Pol IV use different promoters to transcribe the same template.</description><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Base Sequence</subject><subject>Biosynthesis</subject><subject>Botany</subject><subject>DNA Methylation</subject><subject>DNA-directed RNA polymerase</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>enhancer elements</subject><subject>Gene Expression Regulation, Plant</subject><subject>Gene Silencing</subject><subject>Genes, Reporter</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>inverted repeats</subject><subject>loci</subject><subject>Meristem - genetics</subject><subject>Meristem - metabolism</subject><subject>Models, Biological</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Plant Shoots - genetics</subject><subject>Plant Shoots - metabolism</subject><subject>Plants, Genetically Modified</subject><subject>Pol IV</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>reporter genes</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA Polymerase II - genetics</subject><subject>RNA Polymerase II - metabolism</subject><subject>RNA polymerase II</subject><subject>RNA, Plant - genetics</subject><subject>RNA, Plant - metabolism</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA, Small Interfering - metabolism</subject><subject>RNA‐directed DNA methylation</subject><subject>Sequence Analysis</subject><subject>siRNAs</subject><subject>small interfering RNA</subject><subject>tandem repeat sequences</subject><subject>Tandem Repeat Sequences - genetics</subject><subject>tandem repeats</subject><subject>transcription (genetics)</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkcFuEzEQhi0EoqFw4AXAEhcuaT322rs-RoVCUAUVBMTNsr3e1tHGu9jeVrnxCBx4Qp4EJykcOOGLPZrvH2n8IfQUyAmUc5rH9QlQXvF7aAZM8DkD9vU-mhEpyLyugB6hRymtCYGaieohOqJVLRtW1zP085VP2QebsQ4ttkOwU4wuZDzqfH2rtwkPHb4cerxc_vr-Yw_tqy-lat3oQruDk__4foGNH65ccMknrMs8HEs_--xvHM5Rh1QiyfcuWBdxP9gpYR_wImrj22HcpfK17r0O-jF60Ok-uSd39zFanb9enb2dX3x4szxbXMy7qiZ8binwxkhSG-ooZ10jO65bQ2oQhlRN1wCjFrh13MiWCllZxwRIIbV0xmh2jF4exo5x-Da5lNXGJ-v6Xgc3TEkB5yCgEUL-H0oa4HVBX_yDrocphrJHoZjkQKncUc_uqMlsXKvG6Dc6btUfMwU4PQC35cu2f_tA1E65KsrVXrlaXb7bP0ri-SHR6UHpq-iT-vyJEqiKd0IaAuw3mx2qGQ</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Sasaki, Taku</creator><creator>Lee, Tzuu‐fen</creator><creator>Liao, Wen‐Wei</creator><creator>Naumann, Ulf</creator><creator>Liao, Jo‐Ling</creator><creator>Eun, Changho</creator><creator>Huang, Ya‐Yi</creator><creator>Fu, Jason L</creator><creator>Chen, Pao‐Yang</creator><creator>Meyers, Blake C</creator><creator>Matzke, Antonius J.M</creator><creator>Matzke, Marjori</creator><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201407</creationdate><title>Distinct and concurrent pathways of Pol II‐ and Pol IV‐dependent siRNA biogenesis at a repetitive trans‐silencer locus in Arabidopsis thaliana</title><author>Sasaki, Taku ; Lee, Tzuu‐fen ; Liao, Wen‐Wei ; Naumann, Ulf ; Liao, Jo‐Ling ; Eun, Changho ; Huang, Ya‐Yi ; Fu, Jason L ; Chen, Pao‐Yang ; Meyers, Blake C ; Matzke, Antonius J.M ; Matzke, Marjori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f4705-c2158b907b2e253f89f5adb0716b048f8132c15ce5b9d2694ce361969a9ebba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Base Sequence</topic><topic>Biosynthesis</topic><topic>Botany</topic><topic>DNA Methylation</topic><topic>DNA-directed RNA polymerase</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>enhancer elements</topic><topic>Gene Expression Regulation, Plant</topic><topic>Gene Silencing</topic><topic>Genes, Reporter</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>inverted repeats</topic><topic>loci</topic><topic>Meristem - genetics</topic><topic>Meristem - metabolism</topic><topic>Models, Biological</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Plant Shoots - genetics</topic><topic>Plant Shoots - metabolism</topic><topic>Plants, Genetically Modified</topic><topic>Pol IV</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>reporter genes</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA Polymerase II - genetics</topic><topic>RNA Polymerase II - metabolism</topic><topic>RNA polymerase II</topic><topic>RNA, Plant - genetics</topic><topic>RNA, Plant - metabolism</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - metabolism</topic><topic>RNA‐directed DNA methylation</topic><topic>Sequence Analysis</topic><topic>siRNAs</topic><topic>small interfering RNA</topic><topic>tandem repeat sequences</topic><topic>Tandem Repeat Sequences - genetics</topic><topic>tandem repeats</topic><topic>transcription (genetics)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasaki, Taku</creatorcontrib><creatorcontrib>Lee, Tzuu‐fen</creatorcontrib><creatorcontrib>Liao, Wen‐Wei</creatorcontrib><creatorcontrib>Naumann, Ulf</creatorcontrib><creatorcontrib>Liao, Jo‐Ling</creatorcontrib><creatorcontrib>Eun, Changho</creatorcontrib><creatorcontrib>Huang, Ya‐Yi</creatorcontrib><creatorcontrib>Fu, Jason L</creatorcontrib><creatorcontrib>Chen, Pao‐Yang</creatorcontrib><creatorcontrib>Meyers, Blake C</creatorcontrib><creatorcontrib>Matzke, Antonius J.M</creatorcontrib><creatorcontrib>Matzke, Marjori</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasaki, Taku</au><au>Lee, Tzuu‐fen</au><au>Liao, Wen‐Wei</au><au>Naumann, Ulf</au><au>Liao, Jo‐Ling</au><au>Eun, Changho</au><au>Huang, Ya‐Yi</au><au>Fu, Jason L</au><au>Chen, Pao‐Yang</au><au>Meyers, Blake C</au><au>Matzke, Antonius J.M</au><au>Matzke, Marjori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct and concurrent pathways of Pol II‐ and Pol IV‐dependent siRNA biogenesis at a repetitive trans‐silencer locus in Arabidopsis thaliana</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2014-07</date><risdate>2014</risdate><volume>79</volume><issue>1</issue><spage>127</spage><epage>138</epage><pages>127-138</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Short interfering RNAs (siRNAs) homologous to transcriptional regulatory regions can induce RNA‐directed DNA methylation (RdDM) and transcriptional gene silencing (TGS) of target genes. In our system, siRNAs are produced by transcribing an inverted DNA repeat (IR) of enhancer sequences, yielding a hairpin RNA that is processed by several Dicer activities into siRNAs of 21–24 nt. Primarily 24‐nt siRNAs trigger RdDM of the target enhancer in trans and TGS of a downstream GFP reporter gene. We analyzed siRNA accumulation from two different structural forms of a trans‐silencer locus in which tandem repeats are embedded in the enhancer IR and distinguished distinct RNA polymerase II (Pol II)‐ and Pol IV‐dependent pathways of siRNA biogenesis. At the original silencer locus, Pol‐II transcription of the IR from a 35S promoter produces a hairpin RNA that is diced into abundant siRNAs of 21–24 nt. A silencer variant lacking the 35S promoter revealed a normally masked Pol IV‐dependent pathway that produces low levels of 24‐nt siRNAs from the tandem repeats. Both pathways operate concurrently at the original silencer locus. siRNAs accrue only from specific regions of the enhancer and embedded tandem repeat. Analysis of these sequences and endogenous tandem repeats producing siRNAs revealed the preferential accumulation of siRNAs at GC‐rich regions containing methylated CG dinucleotides. In addition to supporting a correlation between base composition, DNA methylation and siRNA accumulation, our results highlight the complexity of siRNA biogenesis at repetitive loci and show that Pol II and Pol IV use different promoters to transcribe the same template.</abstract><cop>England</cop><pub>Blackwell Science</pub><pmid>24798377</pmid><doi>10.1111/tpj.12545</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Base Sequence Biosynthesis Botany DNA Methylation DNA-directed RNA polymerase DNA-Directed RNA Polymerases - genetics DNA-Directed RNA Polymerases - metabolism enhancer elements Gene Expression Regulation, Plant Gene Silencing Genes, Reporter High-Throughput Nucleotide Sequencing inverted repeats loci Meristem - genetics Meristem - metabolism Models, Biological Molecular Sequence Data Mutation Plant Shoots - genetics Plant Shoots - metabolism Plants, Genetically Modified Pol IV Promoter Regions, Genetic - genetics reporter genes Ribonucleic acid RNA RNA Polymerase II - genetics RNA Polymerase II - metabolism RNA polymerase II RNA, Plant - genetics RNA, Plant - metabolism RNA, Small Interfering - genetics RNA, Small Interfering - metabolism RNA‐directed DNA methylation Sequence Analysis siRNAs small interfering RNA tandem repeat sequences Tandem Repeat Sequences - genetics tandem repeats transcription (genetics) |
title | Distinct and concurrent pathways of Pol II‐ and Pol IV‐dependent siRNA biogenesis at a repetitive trans‐silencer locus in Arabidopsis thaliana |
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