The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data

MicroRNAs (miRNAs) regulate gene expression posttranscriptionally. Although previous efforts have demonstrated the functional importance of target sites on miRNAs, little is known about the influence of the rest of 3′ untranslated regions (3′UTRs) of target genes on microRNA function. We conducted a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of genomics 2011, Vol.2011 (2011), p.1-9
Hauptverfasser: Hu, Zihua, Bruno, Andrew E.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 9
container_issue 2011
container_start_page 1
container_title International journal of genomics
container_volume 2011
creator Hu, Zihua
Bruno, Andrew E.
description MicroRNAs (miRNAs) regulate gene expression posttranscriptionally. Although previous efforts have demonstrated the functional importance of target sites on miRNAs, little is known about the influence of the rest of 3′ untranslated regions (3′UTRs) of target genes on microRNA function. We conducted a genome-wide study and found that the entire 3′UTR sequences could also play important roles on miRNA function in addition to miRNA target sites. This was evidenced by the fact that human single nucleotide polymorphisms (SNPs) on both seed target region and the rest of 3′UTRs of miRNA target genes were under significantly stronger negative selection, when compared to non-miRNA target genes. We also discovered that the flanking nucleotides on both sides of miRNA target sites were subject to moderate strong selection. A local sequence region of ~67 nucleotides with symmetric structure is herein defined. Additionally, from gene expression analysis, we found that SNPs and miRNA target sites on target sequences may interactively affect gene expression.
doi_str_mv 10.1155/2011/910769
format Article
fullrecord <record><control><sourceid>emarefa</sourceid><recordid>TN_cdi_emarefa_primary_990493</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>990493</sourcerecordid><originalsourceid>FETCH-emarefa_primary_9904933</originalsourceid><addsrcrecordid>eNpjYBA2NNAzNDQ11TcyMDTUtzQ0MDezZGLgNDI2NNE1MTa3YIGzzSI4GHiLi7MMgMDS2NLC1IyTwTskI1XBMy8tpzQ1LzlVIT9NwfhRw6bQkKBihfw8Bd_M5KL8ID9HBbfSvOSSTKAIUGlqUVFqikJaUX6ugkdpbmKeQrBfgIJLYkkiDwNrWmJOcSovlOZmkHVzDXH20E3NTSxKTUuMLyjKBLIq4y0tDUwsjY0JyQMAXdA-Ew</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data</title><source>Wiley-Blackwell Open Access Titles</source><source>Alma/SFX Local Collection</source><creator>Hu, Zihua ; Bruno, Andrew E.</creator><creatorcontrib>Hu, Zihua ; Bruno, Andrew E.</creatorcontrib><description>MicroRNAs (miRNAs) regulate gene expression posttranscriptionally. Although previous efforts have demonstrated the functional importance of target sites on miRNAs, little is known about the influence of the rest of 3′ untranslated regions (3′UTRs) of target genes on microRNA function. We conducted a genome-wide study and found that the entire 3′UTR sequences could also play important roles on miRNA function in addition to miRNA target sites. This was evidenced by the fact that human single nucleotide polymorphisms (SNPs) on both seed target region and the rest of 3′UTRs of miRNA target genes were under significantly stronger negative selection, when compared to non-miRNA target genes. We also discovered that the flanking nucleotides on both sides of miRNA target sites were subject to moderate strong selection. A local sequence region of ~67 nucleotides with symmetric structure is herein defined. Additionally, from gene expression analysis, we found that SNPs and miRNA target sites on target sequences may interactively affect gene expression.</description><identifier>ISSN: 2314-436X</identifier><identifier>EISSN: 2314-4378</identifier><identifier>DOI: 10.1155/2011/910769</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><ispartof>International journal of genomics, 2011, Vol.2011 (2011), p.1-9</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Hu, Zihua</creatorcontrib><creatorcontrib>Bruno, Andrew E.</creatorcontrib><title>The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data</title><title>International journal of genomics</title><description>MicroRNAs (miRNAs) regulate gene expression posttranscriptionally. Although previous efforts have demonstrated the functional importance of target sites on miRNAs, little is known about the influence of the rest of 3′ untranslated regions (3′UTRs) of target genes on microRNA function. We conducted a genome-wide study and found that the entire 3′UTR sequences could also play important roles on miRNA function in addition to miRNA target sites. This was evidenced by the fact that human single nucleotide polymorphisms (SNPs) on both seed target region and the rest of 3′UTRs of miRNA target genes were under significantly stronger negative selection, when compared to non-miRNA target genes. We also discovered that the flanking nucleotides on both sides of miRNA target sites were subject to moderate strong selection. A local sequence region of ~67 nucleotides with symmetric structure is herein defined. Additionally, from gene expression analysis, we found that SNPs and miRNA target sites on target sequences may interactively affect gene expression.</description><issn>2314-436X</issn><issn>2314-4378</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpjYBA2NNAzNDQ11TcyMDTUtzQ0MDezZGLgNDI2NNE1MTa3YIGzzSI4GHiLi7MMgMDS2NLC1IyTwTskI1XBMy8tpzQ1LzlVIT9NwfhRw6bQkKBihfw8Bd_M5KL8ID9HBbfSvOSSTKAIUGlqUVFqikJaUX6ugkdpbmKeQrBfgIJLYkkiDwNrWmJOcSovlOZmkHVzDXH20E3NTSxKTUuMLyjKBLIq4y0tDUwsjY0JyQMAXdA-Ew</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Hu, Zihua</creator><creator>Bruno, Andrew E.</creator><general>Hindawi Publishing Corporation</general><scope>ADJCN</scope><scope>AHFXO</scope></search><sort><creationdate>2011</creationdate><title>The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data</title><author>Hu, Zihua ; Bruno, Andrew E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-emarefa_primary_9904933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Zihua</creatorcontrib><creatorcontrib>Bruno, Andrew E.</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><jtitle>International journal of genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Zihua</au><au>Bruno, Andrew E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data</atitle><jtitle>International journal of genomics</jtitle><date>2011</date><risdate>2011</risdate><volume>2011</volume><issue>2011</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>2314-436X</issn><eissn>2314-4378</eissn><abstract>MicroRNAs (miRNAs) regulate gene expression posttranscriptionally. Although previous efforts have demonstrated the functional importance of target sites on miRNAs, little is known about the influence of the rest of 3′ untranslated regions (3′UTRs) of target genes on microRNA function. We conducted a genome-wide study and found that the entire 3′UTR sequences could also play important roles on miRNA function in addition to miRNA target sites. This was evidenced by the fact that human single nucleotide polymorphisms (SNPs) on both seed target region and the rest of 3′UTRs of miRNA target genes were under significantly stronger negative selection, when compared to non-miRNA target genes. We also discovered that the flanking nucleotides on both sides of miRNA target sites were subject to moderate strong selection. A local sequence region of ~67 nucleotides with symmetric structure is herein defined. Additionally, from gene expression analysis, we found that SNPs and miRNA target sites on target sequences may interactively affect gene expression.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><doi>10.1155/2011/910769</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 2314-436X
ispartof International journal of genomics, 2011, Vol.2011 (2011), p.1-9
issn 2314-436X
2314-4378
language eng
recordid cdi_emarefa_primary_990493
source Wiley-Blackwell Open Access Titles; Alma/SFX Local Collection
title The Influence of 3′UTRs on MicroRNA Function Inferred from Human SNP Data
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T12%3A39%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-emarefa&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Influence%20of%203%E2%80%B2UTRs%20on%20MicroRNA%20Function%20Inferred%20from%20Human%20SNP%20Data&rft.jtitle=International%20journal%20of%20genomics&rft.au=Hu,%20Zihua&rft.date=2011&rft.volume=2011&rft.issue=2011&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=2314-436X&rft.eissn=2314-4378&rft_id=info:doi/10.1155/2011/910769&rft_dat=%3Cemarefa%3E990493%3C/emarefa%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true