Comparative and functional analysis of intron-mediated enhancement signals reveals conserved features among plants
Introns in a wide range of organisms including plants, animals and fungi are able to increase the expression of the gene that they are contained in. This process of intron-mediated enhancement (IME) is most thoroughly studied in Arabidopsis thaliana, where it has been shown that enhancing introns ar...
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Veröffentlicht in: | Nucleic acids research 2011-07, Vol.39 (13), p.5328-5337 |
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creator | Parra, G. Bradnam, K. Rose, Alan B. Korf, Ian |
description | Introns in a wide range of organisms including plants, animals and fungi are able to increase the expression of the gene that they are contained in. This process of intron-mediated enhancement (IME) is most thoroughly studied in Arabidopsis thaliana, where it has been shown that enhancing introns are typically located near the promoter and are compositionally distinct from downstream introns. In this study, we perform a comprehensive comparative analysis of several sequenced plant genomes. We find that enhancing sequences are conserved in the multi-cellular plants but are either absent or unrecognizable in algae. IME signals are preferentially located towards the 5′-end of first introns but also appear to be enriched in 5′-UTRs and coding regions near the transcription start site. Enhancing introns are found most prominently in genes that are highly expressed in a wide range of tissues. Through site-directed mutagenesis in A. thaliana, we show that IME signals can be inserted or removed from introns to increase or decrease gene expression. Although we do not yet know the specific mechanism of IME, the predicted signals appear to be both functional and highly conserved. |
doi_str_mv | 10.1093/nar/gkr043 |
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This process of intron-mediated enhancement (IME) is most thoroughly studied in Arabidopsis thaliana, where it has been shown that enhancing introns are typically located near the promoter and are compositionally distinct from downstream introns. In this study, we perform a comprehensive comparative analysis of several sequenced plant genomes. We find that enhancing sequences are conserved in the multi-cellular plants but are either absent or unrecognizable in algae. IME signals are preferentially located towards the 5′-end of first introns but also appear to be enriched in 5′-UTRs and coding regions near the transcription start site. Enhancing introns are found most prominently in genes that are highly expressed in a wide range of tissues. Through site-directed mutagenesis in A. thaliana, we show that IME signals can be inserted or removed from introns to increase or decrease gene expression. Although we do not yet know the specific mechanism of IME, the predicted signals appear to be both functional and highly conserved.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkr043</identifier><identifier>PMID: 21427088</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>5' Untranslated Regions ; Algae ; Arabidopsis - genetics ; Arabidopsis thaliana ; Computational Biology ; Gene Expression Regulation, Plant ; Introns ; Oryza - genetics ; Regulatory Elements, Transcriptional</subject><ispartof>Nucleic acids research, 2011-07, Vol.39 (13), p.5328-5337</ispartof><rights>The Author(s) 2011. 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This process of intron-mediated enhancement (IME) is most thoroughly studied in Arabidopsis thaliana, where it has been shown that enhancing introns are typically located near the promoter and are compositionally distinct from downstream introns. In this study, we perform a comprehensive comparative analysis of several sequenced plant genomes. We find that enhancing sequences are conserved in the multi-cellular plants but are either absent or unrecognizable in algae. IME signals are preferentially located towards the 5′-end of first introns but also appear to be enriched in 5′-UTRs and coding regions near the transcription start site. Enhancing introns are found most prominently in genes that are highly expressed in a wide range of tissues. Through site-directed mutagenesis in A. thaliana, we show that IME signals can be inserted or removed from introns to increase or decrease gene expression. Although we do not yet know the specific mechanism of IME, the predicted signals appear to be both functional and highly conserved.</description><subject>5' Untranslated Regions</subject><subject>Algae</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis thaliana</subject><subject>Computational Biology</subject><subject>Gene Expression Regulation, Plant</subject><subject>Introns</subject><subject>Oryza - genetics</subject><subject>Regulatory Elements, Transcriptional</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU-LFDEQxYMo7uzqxQ8guYiw0G6STro7F2EZ_AcLXvQcqtOV2Wh30ibpgf32Zpl10Yunoqgfr17VI-QVZ-840-1VgHR1-JmYbJ-QHW870Ujdiadkx1qmGs7kcEbOc_7BGJdcyefkTHApejYMO5L2cVkhQfFHpBAm6rZgi48B5trCfJd9ptFRH0qKoVlw8lBwohhuIVhcMBSa_aGSmSY84n21MWRMx0o5hLIlzBSWGA50nSGU_II8cxXDlw_1gnz_-OHb_nNz8_XTl_31TWMVU6VRspsmtK3TqkfusB8Vs5aDmzifRDtKIUet5IB6VMPQd4hKIEfHmAQuQLQX5P1Jd93G6ttWqwlmsya_QLozEbz5dxL8rTnEo2nrm4TQVeDtg0CKvzbMxSw-W5zrFRi3bAatec963VXy8kTaFHNO6B63cGbuMzI1I3PKqMKv__b1iP4JpQJvTkDc1v8J_QZNoJ8Q</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Parra, G.</creator><creator>Bradnam, K.</creator><creator>Rose, Alan B.</creator><creator>Korf, Ian</creator><general>Oxford University Press</general><scope>TOX</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>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20110701</creationdate><title>Comparative and functional analysis of intron-mediated enhancement signals reveals conserved features among plants</title><author>Parra, G. ; Bradnam, K. ; Rose, Alan B. ; Korf, Ian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-546ddec3f957e1fe7b50cc1afd11d23b424b9548e9b58876ee52e1ef004a12a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>5' Untranslated Regions</topic><topic>Algae</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis thaliana</topic><topic>Computational Biology</topic><topic>Gene Expression Regulation, Plant</topic><topic>Introns</topic><topic>Oryza - genetics</topic><topic>Regulatory Elements, Transcriptional</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parra, G.</creatorcontrib><creatorcontrib>Bradnam, K.</creatorcontrib><creatorcontrib>Rose, Alan B.</creatorcontrib><creatorcontrib>Korf, Ian</creatorcontrib><collection>Oxford Journals Open Access Collection</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>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>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parra, G.</au><au>Bradnam, K.</au><au>Rose, Alan B.</au><au>Korf, Ian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative and functional analysis of intron-mediated enhancement signals reveals conserved features among plants</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>39</volume><issue>13</issue><spage>5328</spage><epage>5337</epage><pages>5328-5337</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Introns in a wide range of organisms including plants, animals and fungi are able to increase the expression of the gene that they are contained in. This process of intron-mediated enhancement (IME) is most thoroughly studied in Arabidopsis thaliana, where it has been shown that enhancing introns are typically located near the promoter and are compositionally distinct from downstream introns. In this study, we perform a comprehensive comparative analysis of several sequenced plant genomes. We find that enhancing sequences are conserved in the multi-cellular plants but are either absent or unrecognizable in algae. IME signals are preferentially located towards the 5′-end of first introns but also appear to be enriched in 5′-UTRs and coding regions near the transcription start site. Enhancing introns are found most prominently in genes that are highly expressed in a wide range of tissues. Through site-directed mutagenesis in A. thaliana, we show that IME signals can be inserted or removed from introns to increase or decrease gene expression. Although we do not yet know the specific mechanism of IME, the predicted signals appear to be both functional and highly conserved.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>21427088</pmid><doi>10.1093/nar/gkr043</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 5' Untranslated Regions Algae Arabidopsis - genetics Arabidopsis thaliana Computational Biology Gene Expression Regulation, Plant Introns Oryza - genetics Regulatory Elements, Transcriptional |
title | Comparative and functional analysis of intron-mediated enhancement signals reveals conserved features among plants |
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