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Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription

We have examined the nuclear localization of transiently and stably expressed nascent RNA transcripts containing or lacking introns in order to determine if the spatial association of RNA transcripts and pre-mRNA splicing factors in nuclei is random or functionally significant. Our findings show tha...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120843/
https://www.ncbi.nlm.nih.gov/pubmed/8666659
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collection PubMed
description We have examined the nuclear localization of transiently and stably expressed nascent RNA transcripts containing or lacking introns in order to determine if the spatial association of RNA transcripts and pre-mRNA splicing factors in nuclei is random or functionally significant. Our findings show that the association between nascent RNA and splicing factors in the nucleus is intron-dependent when the RNAs are either transiently or stably expressed. Furthermore, our data indicate that splicing factors are recruited to the transcription sites. The presence of both pre-and mRNA at these locations suggest that pre-mRNA splicing occurs at these sites of transcription. In addition, electron microscopic examination of the highly active transcription sites has revealed a granular appearance which closely resembles, but is functionally different from, interchromatin granule clusters. Our findings demonstrate that the nucleus is highly organized and dynamic with regard to the functions of the transcription and pre- mRNA splicing.
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spelling pubmed-21208432008-05-01 Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription J Cell Biol Articles We have examined the nuclear localization of transiently and stably expressed nascent RNA transcripts containing or lacking introns in order to determine if the spatial association of RNA transcripts and pre-mRNA splicing factors in nuclei is random or functionally significant. Our findings show that the association between nascent RNA and splicing factors in the nucleus is intron-dependent when the RNAs are either transiently or stably expressed. Furthermore, our data indicate that splicing factors are recruited to the transcription sites. The presence of both pre-and mRNA at these locations suggest that pre-mRNA splicing occurs at these sites of transcription. In addition, electron microscopic examination of the highly active transcription sites has revealed a granular appearance which closely resembles, but is functionally different from, interchromatin granule clusters. Our findings demonstrate that the nucleus is highly organized and dynamic with regard to the functions of the transcription and pre- mRNA splicing. The Rockefeller University Press 1996-05-02 /pmc/articles/PMC2120843/ /pubmed/8666659 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title_full Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title_fullStr Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title_full_unstemmed Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title_short Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription
title_sort intron-dependent recruitment of pre-mrna splicing factors to sites of transcription
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2120843/
https://www.ncbi.nlm.nih.gov/pubmed/8666659