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
Hauptverfasser: Kaneström, A, Andresen, V, Szilvay, A. M, Kalland, K.-H, Haukenes, G
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container_start_page 279
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creator Kaneström, A
Andresen, V
Szilvay, A. M
Kalland, K.-H
Haukenes, G
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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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. 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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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source MEDLINE; SpringerNature Journals
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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