Histographic recording of human immunodeficiency virus type 1 (HIV-1) regulatory protein Rev and nuclear factors
HeLa cells and HeLa cells expressing the HIV-1 regulatory protein Rev were immunostained for Rev and pre-mRNA processing factors and examined histographically by confocal laser scanning microscopy. Following short pulse-labelling with bromouridine tri-phosphate nascent RNA gave a granular nucleoplas...
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Veröffentlicht in: | Archives of virology 1998-01, Vol.143 (2), p.279-294 |
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description | HeLa cells and HeLa cells expressing the HIV-1 regulatory protein Rev were immunostained for Rev and pre-mRNA processing factors and examined histographically by confocal laser scanning microscopy. Following short pulse-labelling with bromouridine tri-phosphate nascent RNA gave a granular nucleoplasmic staining increasing somewhat towards the periphery as did also the heterogeneous ribonucleoproteins (hnRNPs) Aff1 and particularly C1/C2, a distribution pattern which has not been described. The sm-antigen of the small ribonucleoprotein particle (snRNP) proteins U1, U2, U4/U6 and U5 stained the nucleoplasm diffusely in addition to speckles which co-localised with speckles of the non-snRNP splicing factor SC-35. Brominated RNA and the hnRNPs Aff1 and C1/C2 were to varying degrees excluded from the speckles. Rev concentrated in the nucleolus and often as a perinucleolar ring/zone. Rev also stained the nucleoplasm and cytoplasm without co-localising with the above-mentioned proteins or brominated RNA and was not enriched or excluded in SC-35 speckles. The nucleolar proteins B23 and C23, like Rev, gave primarily a perinucleolar ring and stained the nucleoplasm but did not otherwise co-localise with Rev or with nuclear proteins. Histographic recording of immunofluorescence images proved to be a valuable tool in the study of localisation of HIV-1 Rev and cellular components and of possible co-localisations. A parallel comparison of the subcellular patterns of pre-mRNA processing factors versus major nucleolar antigens is new and suggests that the factors are not strictly separated in the nucleoplasm. |
doi_str_mv | 10.1007/s007050050286 |
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M ; Kalland, K.-H ; Haukenes, G</creator><creatorcontrib>Kaneström, A ; Andresen, V ; Szilvay, A. M ; Kalland, K.-H ; Haukenes, G</creatorcontrib><description>HeLa cells and HeLa cells expressing the HIV-1 regulatory protein Rev were immunostained for Rev and pre-mRNA processing factors and examined histographically by confocal laser scanning microscopy. Following short pulse-labelling with bromouridine tri-phosphate nascent RNA gave a granular nucleoplasmic staining increasing somewhat towards the periphery as did also the heterogeneous ribonucleoproteins (hnRNPs) Aff1 and particularly C1/C2, a distribution pattern which has not been described. The sm-antigen of the small ribonucleoprotein particle (snRNP) proteins U1, U2, U4/U6 and U5 stained the nucleoplasm diffusely in addition to speckles which co-localised with speckles of the non-snRNP splicing factor SC-35. Brominated RNA and the hnRNPs Aff1 and C1/C2 were to varying degrees excluded from the speckles. Rev concentrated in the nucleolus and often as a perinucleolar ring/zone. Rev also stained the nucleoplasm and cytoplasm without co-localising with the above-mentioned proteins or brominated RNA and was not enriched or excluded in SC-35 speckles. The nucleolar proteins B23 and C23, like Rev, gave primarily a perinucleolar ring and stained the nucleoplasm but did not otherwise co-localise with Rev or with nuclear proteins. Histographic recording of immunofluorescence images proved to be a valuable tool in the study of localisation of HIV-1 Rev and cellular components and of possible co-localisations. A parallel comparison of the subcellular patterns of pre-mRNA processing factors versus major nucleolar antigens is new and suggests that the factors are not strictly separated in the nucleoplasm.</description><identifier>ISSN: 0304-8608</identifier><identifier>EISSN: 1432-8798</identifier><identifier>DOI: 10.1007/s007050050286</identifier><identifier>PMID: 9541613</identifier><language>eng</language><publisher>Wien: Springer-Verlag</publisher><subject>AIDS/HIV ; Animals ; antigens ; Biological and medical sciences ; bromination ; Bromodeoxyuridine - metabolism ; cell nucleolus ; Cells ; confocal laser scanning microscopy ; cytoplasm ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; Gene Products, rev - analysis ; HeLa Cells ; HIV ; HIV-1 - chemistry ; Human immunodeficiency virus ; Humans ; Immunohistochemistry ; Mice ; Microbiology ; nuclear proteins ; Nuclear Proteins - analysis ; Proteins ; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains ; rev Gene Products, Human Immunodeficiency Virus ; ribonucleoproteins ; RNA ; RNA, Messenger - metabolism ; RNA, Viral - analysis ; Transfection ; Virology</subject><ispartof>Archives of virology, 1998-01, Vol.143 (2), p.279-294</ispartof><rights>1998 INIST-CNRS</rights><rights>1998 Springer-Verlag/ Wien</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-5a2551b86a1384e0bbc8fffa20dd5fe681c5e701605b3933203ae27963e845043</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2188200$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9541613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaneström, A</creatorcontrib><creatorcontrib>Andresen, V</creatorcontrib><creatorcontrib>Szilvay, A. M</creatorcontrib><creatorcontrib>Kalland, K.-H</creatorcontrib><creatorcontrib>Haukenes, G</creatorcontrib><title>Histographic recording of human immunodeficiency virus type 1 (HIV-1) regulatory protein Rev and nuclear factors</title><title>Archives of virology</title><addtitle>Arch Virol</addtitle><description>HeLa cells and HeLa cells expressing the HIV-1 regulatory protein Rev were immunostained for Rev and pre-mRNA processing factors and examined histographically by confocal laser scanning microscopy. Following short pulse-labelling with bromouridine tri-phosphate nascent RNA gave a granular nucleoplasmic staining increasing somewhat towards the periphery as did also the heterogeneous ribonucleoproteins (hnRNPs) Aff1 and particularly C1/C2, a distribution pattern which has not been described. The sm-antigen of the small ribonucleoprotein particle (snRNP) proteins U1, U2, U4/U6 and U5 stained the nucleoplasm diffusely in addition to speckles which co-localised with speckles of the non-snRNP splicing factor SC-35. Brominated RNA and the hnRNPs Aff1 and C1/C2 were to varying degrees excluded from the speckles. Rev concentrated in the nucleolus and often as a perinucleolar ring/zone. Rev also stained the nucleoplasm and cytoplasm without co-localising with the above-mentioned proteins or brominated RNA and was not enriched or excluded in SC-35 speckles. The nucleolar proteins B23 and C23, like Rev, gave primarily a perinucleolar ring and stained the nucleoplasm but did not otherwise co-localise with Rev or with nuclear proteins. Histographic recording of immunofluorescence images proved to be a valuable tool in the study of localisation of HIV-1 Rev and cellular components and of possible co-localisations. A parallel comparison of the subcellular patterns of pre-mRNA processing factors versus major nucleolar antigens is new and suggests that the factors are not strictly separated in the nucleoplasm.</description><subject>AIDS/HIV</subject><subject>Animals</subject><subject>antigens</subject><subject>Biological and medical sciences</subject><subject>bromination</subject><subject>Bromodeoxyuridine - metabolism</subject><subject>cell nucleolus</subject><subject>Cells</subject><subject>confocal laser scanning microscopy</subject><subject>cytoplasm</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Products, rev - analysis</subject><subject>HeLa Cells</subject><subject>HIV</subject><subject>HIV-1 - chemistry</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Mice</subject><subject>Microbiology</subject><subject>nuclear proteins</subject><subject>Nuclear Proteins - analysis</subject><subject>Proteins</subject><subject>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</subject><subject>rev Gene Products, Human Immunodeficiency Virus</subject><subject>ribonucleoproteins</subject><subject>RNA</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Viral - analysis</subject><subject>Transfection</subject><subject>Virology</subject><issn>0304-8608</issn><issn>1432-8798</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkU2LFDEQhoMo6zh69CgGFNFDa-Wz00dZ1FlYENT12qTTyWyW7qQ36SzMvzfLDAt6EYoqyPukUpUXoZcEPhKA9lOuCQTUoEo-QhvCGW1U26nHaAMMeKMkqKfoWc43APWAiTN01glOJGEbtOx8XuM-6eXaG5ysiWn0YY-jw9dl1gH7eS4hjtZ5420wB3znU8l4PSwWE_x-d_G7IR_qxX2Z9BrTAS8prtYH_MPeYR1GHIqZrE7YaVP1_Bw9cXrK9sWpbtHV1y-_znfN5fdvF-efLxvDAdZGaCoEGZTUhCluYRiMcs5pCuMonJWKGGFbIBLEwDrGKDBtadtJZhUXwNkWvTv2rfPcFpvXfvbZ2GnSwcaS-7ZrlVKU_RckkoNq-T345h_wJpYU6hI9AUW4qM_SSjVHyqSYc7KuX5KfdTpUqL83rP_LsMq_OnUtw2zHB_rkUNXfnnSdjZ5c0sH4_IBRUpeotm7R6yPmdOz1PlXk6icFUj8TpJQdYX8An2qkiw</recordid><startdate>19980101</startdate><enddate>19980101</enddate><creator>Kaneström, A</creator><creator>Andresen, V</creator><creator>Szilvay, A. 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Psychology</topic><topic>Gene Products, rev - analysis</topic><topic>HeLa Cells</topic><topic>HIV</topic><topic>HIV-1 - chemistry</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Mice</topic><topic>Microbiology</topic><topic>nuclear proteins</topic><topic>Nuclear Proteins - analysis</topic><topic>Proteins</topic><topic>Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains</topic><topic>rev Gene Products, Human Immunodeficiency Virus</topic><topic>ribonucleoproteins</topic><topic>RNA</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Viral - analysis</topic><topic>Transfection</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaneström, A</creatorcontrib><creatorcontrib>Andresen, V</creatorcontrib><creatorcontrib>Szilvay, A. 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M</au><au>Kalland, K.-H</au><au>Haukenes, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histographic recording of human immunodeficiency virus type 1 (HIV-1) regulatory protein Rev and nuclear factors</atitle><jtitle>Archives of virology</jtitle><addtitle>Arch Virol</addtitle><date>1998-01-01</date><risdate>1998</risdate><volume>143</volume><issue>2</issue><spage>279</spage><epage>294</epage><pages>279-294</pages><issn>0304-8608</issn><eissn>1432-8798</eissn><abstract>HeLa cells and HeLa cells expressing the HIV-1 regulatory protein Rev were immunostained for Rev and pre-mRNA processing factors and examined histographically by confocal laser scanning microscopy. Following short pulse-labelling with bromouridine tri-phosphate nascent RNA gave a granular nucleoplasmic staining increasing somewhat towards the periphery as did also the heterogeneous ribonucleoproteins (hnRNPs) Aff1 and particularly C1/C2, a distribution pattern which has not been described. The sm-antigen of the small ribonucleoprotein particle (snRNP) proteins U1, U2, U4/U6 and U5 stained the nucleoplasm diffusely in addition to speckles which co-localised with speckles of the non-snRNP splicing factor SC-35. Brominated RNA and the hnRNPs Aff1 and C1/C2 were to varying degrees excluded from the speckles. Rev concentrated in the nucleolus and often as a perinucleolar ring/zone. Rev also stained the nucleoplasm and cytoplasm without co-localising with the above-mentioned proteins or brominated RNA and was not enriched or excluded in SC-35 speckles. The nucleolar proteins B23 and C23, like Rev, gave primarily a perinucleolar ring and stained the nucleoplasm but did not otherwise co-localise with Rev or with nuclear proteins. Histographic recording of immunofluorescence images proved to be a valuable tool in the study of localisation of HIV-1 Rev and cellular components and of possible co-localisations. A parallel comparison of the subcellular patterns of pre-mRNA processing factors versus major nucleolar antigens is new and suggests that the factors are not strictly separated in the nucleoplasm.</abstract><cop>Wien</cop><cop>New York, NY</cop><pub>Springer-Verlag</pub><pmid>9541613</pmid><doi>10.1007/s007050050286</doi><tpages>16</tpages></addata></record> |
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subjects | AIDS/HIV Animals antigens Biological and medical sciences bromination Bromodeoxyuridine - metabolism cell nucleolus Cells confocal laser scanning microscopy cytoplasm Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Gene Products, rev - analysis HeLa Cells HIV HIV-1 - chemistry Human immunodeficiency virus Humans Immunohistochemistry Mice Microbiology nuclear proteins Nuclear Proteins - analysis Proteins Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains rev Gene Products, Human Immunodeficiency Virus ribonucleoproteins RNA RNA, Messenger - metabolism RNA, Viral - analysis Transfection Virology |
title | Histographic recording of human immunodeficiency virus type 1 (HIV-1) regulatory protein Rev and nuclear factors |
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