A role for TREX components in the release of spliced mRNA from nuclear speckle domains
The TREX complex, which functions in mRNA export, is recruited to mRNA during splicing. Both the splicing machinery and the TREX complex are concentrated in 20–50 discrete foci known as nuclear speckle domains. In this study, we use a model system where DNA constructs are microinjected into HeLa cel...
Gespeichert in:
Veröffentlicht in: | Nature communications 2010-10, Vol.1 (1), p.97-97, Article 97 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 97 |
---|---|
container_issue | 1 |
container_start_page | 97 |
container_title | Nature communications |
container_volume | 1 |
creator | Dias, Anusha P. Dufu, Kobina Lei, Haixin Reed, Robin |
description | The TREX complex, which functions in mRNA export, is recruited to mRNA during splicing. Both the splicing machinery and the TREX complex are concentrated in 20–50 discrete foci known as nuclear speckle domains. In this study, we use a model system where DNA constructs are microinjected into HeLa cell nuclei, to follow the fates of the transcripts. We show that transcripts lacking functional splice sites, which are inefficiently exported, do not associate with nuclear speckle domains but are instead distributed throughout the nucleoplasm. In contrast, pre-mRNAs containing functional splice sites accumulate in nuclear speckles, and our data suggest that splicing occurs in these domains. When the TREX components UAP56 or Aly are knocked down, spliced mRNA, as well as total polyA+ RNA, accumulates in nuclear speckle domains. Together, our data raise the possibility that pre-mRNA undergoes splicing in nuclear speckle domains, before their release by TREX components for efficient export to the cytoplasm.
The pre-mRNA splicing and TREX mRNA export machineries are found in nuclear speckle domains. Dias
et al
. microinject CMV-DNA constructs into cells and find that transcripts containing functional splice sites accumulate in nuclear speckles and that the TREX complex is required to release the mRNA once processed. |
doi_str_mv | 10.1038/ncomms1103 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3793428</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1008831363</sourcerecordid><originalsourceid>FETCH-LOGICAL-c572t-85ec28aa43e15e3ddcc3d3f7b2aff26a35b5ef4bd30e81abcfa4b965f22ae3a3</originalsourceid><addsrcrecordid>eNp9kV1LHDEUhkOpVFn3xh9QQm8Uy2qSMx-ZG2FZtq0gFpZFvAuZzImOnUnWZKfQf29k7a4VaW5y4H14ck4OIUecnXEG8twZ3_eRp_oDORAs4xNeCvj4qt4n4xgfWDpQcZlln8i-YJXkTOQH5GZKg--QWh_ocjG_pUm38g7dOtLW0fU90oAd6ojUWxpXXWuwof3iekpt8D11g0lpSAmaX8nT-F63Lh6SPau7iOOXe0SW3-bL2Y_J1c_vl7Pp1cTkpVhPZI5GSK0zQJ4jNI0x0IAta6GtFYWGvM7RZnUDDCXXtbE6q6sit0JoBA0jcrHRroa6x8aktoPu1Cq0vQ5_lNet-jdx7b26878VlBVkQibB8Ysg-McB41r1bTTYddqhH6IqC5GVsiieyZP_kpwxKYFDAQn98gZ98ENw6R9UJfKqBFlUCTrdQCb4GAPabdecqefNqt1mE_z59Zxb9O8eE_B1A8QUuTsMuyff0T0BvsmvMQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>925973869</pqid></control><display><type>article</type><title>A role for TREX components in the release of spliced mRNA from nuclear speckle domains</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Dias, Anusha P. ; Dufu, Kobina ; Lei, Haixin ; Reed, Robin</creator><creatorcontrib>Dias, Anusha P. ; Dufu, Kobina ; Lei, Haixin ; Reed, Robin</creatorcontrib><description>The TREX complex, which functions in mRNA export, is recruited to mRNA during splicing. Both the splicing machinery and the TREX complex are concentrated in 20–50 discrete foci known as nuclear speckle domains. In this study, we use a model system where DNA constructs are microinjected into HeLa cell nuclei, to follow the fates of the transcripts. We show that transcripts lacking functional splice sites, which are inefficiently exported, do not associate with nuclear speckle domains but are instead distributed throughout the nucleoplasm. In contrast, pre-mRNAs containing functional splice sites accumulate in nuclear speckles, and our data suggest that splicing occurs in these domains. When the TREX components UAP56 or Aly are knocked down, spliced mRNA, as well as total polyA+ RNA, accumulates in nuclear speckle domains. Together, our data raise the possibility that pre-mRNA undergoes splicing in nuclear speckle domains, before their release by TREX components for efficient export to the cytoplasm.
The pre-mRNA splicing and TREX mRNA export machineries are found in nuclear speckle domains. Dias
et al
. microinject CMV-DNA constructs into cells and find that transcripts containing functional splice sites accumulate in nuclear speckles and that the TREX complex is required to release the mRNA once processed.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/ncomms1103</identifier><identifier>PMID: 20981025</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/337/1645/1792 ; 631/45/500 ; 631/45/612/822 ; 631/80/389/2052 ; Cytoplasm ; Data processing ; DEAD-box RNA Helicases - genetics ; DNA ; exports ; HeLa Cells ; Humanities and Social Sciences ; Humans ; In Situ Hybridization, Fluorescence ; Machinery ; multidisciplinary ; Nuclear Proteins - genetics ; Nuclei ; RNA Interference ; RNA Precursors - genetics ; RNA Splicing - genetics ; RNA, Messenger - genetics ; RNA-Binding Proteins - genetics ; Science ; Science (multidisciplinary) ; Splicing ; Transcription Factors - genetics</subject><ispartof>Nature communications, 2010-10, Vol.1 (1), p.97-97, Article 97</ispartof><rights>Springer Nature Limited 2010</rights><rights>Copyright Nature Publishing Group Oct 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-85ec28aa43e15e3ddcc3d3f7b2aff26a35b5ef4bd30e81abcfa4b965f22ae3a3</citedby><cites>FETCH-LOGICAL-c572t-85ec28aa43e15e3ddcc3d3f7b2aff26a35b5ef4bd30e81abcfa4b965f22ae3a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27902,27903</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20981025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dias, Anusha P.</creatorcontrib><creatorcontrib>Dufu, Kobina</creatorcontrib><creatorcontrib>Lei, Haixin</creatorcontrib><creatorcontrib>Reed, Robin</creatorcontrib><title>A role for TREX components in the release of spliced mRNA from nuclear speckle domains</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>The TREX complex, which functions in mRNA export, is recruited to mRNA during splicing. Both the splicing machinery and the TREX complex are concentrated in 20–50 discrete foci known as nuclear speckle domains. In this study, we use a model system where DNA constructs are microinjected into HeLa cell nuclei, to follow the fates of the transcripts. We show that transcripts lacking functional splice sites, which are inefficiently exported, do not associate with nuclear speckle domains but are instead distributed throughout the nucleoplasm. In contrast, pre-mRNAs containing functional splice sites accumulate in nuclear speckles, and our data suggest that splicing occurs in these domains. When the TREX components UAP56 or Aly are knocked down, spliced mRNA, as well as total polyA+ RNA, accumulates in nuclear speckle domains. Together, our data raise the possibility that pre-mRNA undergoes splicing in nuclear speckle domains, before their release by TREX components for efficient export to the cytoplasm.
The pre-mRNA splicing and TREX mRNA export machineries are found in nuclear speckle domains. Dias
et al
. microinject CMV-DNA constructs into cells and find that transcripts containing functional splice sites accumulate in nuclear speckles and that the TREX complex is required to release the mRNA once processed.</description><subject>631/337/1645/1792</subject><subject>631/45/500</subject><subject>631/45/612/822</subject><subject>631/80/389/2052</subject><subject>Cytoplasm</subject><subject>Data processing</subject><subject>DEAD-box RNA Helicases - genetics</subject><subject>DNA</subject><subject>exports</subject><subject>HeLa Cells</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Machinery</subject><subject>multidisciplinary</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclei</subject><subject>RNA Interference</subject><subject>RNA Precursors - genetics</subject><subject>RNA Splicing - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA-Binding Proteins - genetics</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Splicing</subject><subject>Transcription Factors - genetics</subject><issn>2041-1723</issn><issn>2041-1723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kV1LHDEUhkOpVFn3xh9QQm8Uy2qSMx-ZG2FZtq0gFpZFvAuZzImOnUnWZKfQf29k7a4VaW5y4H14ck4OIUecnXEG8twZ3_eRp_oDORAs4xNeCvj4qt4n4xgfWDpQcZlln8i-YJXkTOQH5GZKg--QWh_ocjG_pUm38g7dOtLW0fU90oAd6ojUWxpXXWuwof3iekpt8D11g0lpSAmaX8nT-F63Lh6SPau7iOOXe0SW3-bL2Y_J1c_vl7Pp1cTkpVhPZI5GSK0zQJ4jNI0x0IAta6GtFYWGvM7RZnUDDCXXtbE6q6sit0JoBA0jcrHRroa6x8aktoPu1Cq0vQ5_lNet-jdx7b26878VlBVkQibB8Ysg-McB41r1bTTYddqhH6IqC5GVsiieyZP_kpwxKYFDAQn98gZ98ENw6R9UJfKqBFlUCTrdQCb4GAPabdecqefNqt1mE_z59Zxb9O8eE_B1A8QUuTsMuyff0T0BvsmvMQ</recordid><startdate>20101019</startdate><enddate>20101019</enddate><creator>Dias, Anusha P.</creator><creator>Dufu, Kobina</creator><creator>Lei, Haixin</creator><creator>Reed, Robin</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><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>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20101019</creationdate><title>A role for TREX components in the release of spliced mRNA from nuclear speckle domains</title><author>Dias, Anusha P. ; Dufu, Kobina ; Lei, Haixin ; Reed, Robin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-85ec28aa43e15e3ddcc3d3f7b2aff26a35b5ef4bd30e81abcfa4b965f22ae3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/337/1645/1792</topic><topic>631/45/500</topic><topic>631/45/612/822</topic><topic>631/80/389/2052</topic><topic>Cytoplasm</topic><topic>Data processing</topic><topic>DEAD-box RNA Helicases - genetics</topic><topic>DNA</topic><topic>exports</topic><topic>HeLa Cells</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Machinery</topic><topic>multidisciplinary</topic><topic>Nuclear Proteins - genetics</topic><topic>Nuclei</topic><topic>RNA Interference</topic><topic>RNA Precursors - genetics</topic><topic>RNA Splicing - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA-Binding Proteins - genetics</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Splicing</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dias, Anusha P.</creatorcontrib><creatorcontrib>Dufu, Kobina</creatorcontrib><creatorcontrib>Lei, Haixin</creatorcontrib><creatorcontrib>Reed, Robin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dias, Anusha P.</au><au>Dufu, Kobina</au><au>Lei, Haixin</au><au>Reed, Robin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A role for TREX components in the release of spliced mRNA from nuclear speckle domains</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2010-10-19</date><risdate>2010</risdate><volume>1</volume><issue>1</issue><spage>97</spage><epage>97</epage><pages>97-97</pages><artnum>97</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>The TREX complex, which functions in mRNA export, is recruited to mRNA during splicing. Both the splicing machinery and the TREX complex are concentrated in 20–50 discrete foci known as nuclear speckle domains. In this study, we use a model system where DNA constructs are microinjected into HeLa cell nuclei, to follow the fates of the transcripts. We show that transcripts lacking functional splice sites, which are inefficiently exported, do not associate with nuclear speckle domains but are instead distributed throughout the nucleoplasm. In contrast, pre-mRNAs containing functional splice sites accumulate in nuclear speckles, and our data suggest that splicing occurs in these domains. When the TREX components UAP56 or Aly are knocked down, spliced mRNA, as well as total polyA+ RNA, accumulates in nuclear speckle domains. Together, our data raise the possibility that pre-mRNA undergoes splicing in nuclear speckle domains, before their release by TREX components for efficient export to the cytoplasm.
The pre-mRNA splicing and TREX mRNA export machineries are found in nuclear speckle domains. Dias
et al
. microinject CMV-DNA constructs into cells and find that transcripts containing functional splice sites accumulate in nuclear speckles and that the TREX complex is required to release the mRNA once processed.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>20981025</pmid><doi>10.1038/ncomms1103</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2041-1723 |
ispartof | Nature communications, 2010-10, Vol.1 (1), p.97-97, Article 97 |
issn | 2041-1723 2041-1723 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3793428 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | 631/337/1645/1792 631/45/500 631/45/612/822 631/80/389/2052 Cytoplasm Data processing DEAD-box RNA Helicases - genetics DNA exports HeLa Cells Humanities and Social Sciences Humans In Situ Hybridization, Fluorescence Machinery multidisciplinary Nuclear Proteins - genetics Nuclei RNA Interference RNA Precursors - genetics RNA Splicing - genetics RNA, Messenger - genetics RNA-Binding Proteins - genetics Science Science (multidisciplinary) Splicing Transcription Factors - genetics |
title | A role for TREX components in the release of spliced mRNA from nuclear speckle domains |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T10%3A02%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20role%20for%20TREX%20components%20in%20the%20release%20of%20spliced%20mRNA%20from%20nuclear%20speckle%20domains&rft.jtitle=Nature%20communications&rft.au=Dias,%20Anusha%20P.&rft.date=2010-10-19&rft.volume=1&rft.issue=1&rft.spage=97&rft.epage=97&rft.pages=97-97&rft.artnum=97&rft.issn=2041-1723&rft.eissn=2041-1723&rft_id=info:doi/10.1038/ncomms1103&rft_dat=%3Cproquest_pubme%3E1008831363%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=925973869&rft_id=info:pmid/20981025&rfr_iscdi=true |