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Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors

We have examined the functional significance of the organization of pre- mRNA splicing factors in a speckled distribution in the mammalian cell nucleus. Upon microinjection into living cells of oligonucleotides or antibodies that inhibit pre-mRNA splicing in vitro, we observed major changes in the o...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119927/
https://www.ncbi.nlm.nih.gov/pubmed/8294510
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description We have examined the functional significance of the organization of pre- mRNA splicing factors in a speckled distribution in the mammalian cell nucleus. Upon microinjection into living cells of oligonucleotides or antibodies that inhibit pre-mRNA splicing in vitro, we observed major changes in the organization of splicing factors in vivo. Interchromatin granule clusters became uniform in shape, decreased in number, and increased in both size and content of splicing factors, as measured by immunofluorescence. These changes were transient and the organization of splicing factors returned to their normal distribution by 24 h following microinjection. Microinjection of these oligonucleotides or antibodies also resulted in a reduction of transcription in vivo, but the oligonucleotides did not inhibit transcription in vitro. Control oligonucleotides did not disrupt splicing or transcription in vivo. We propose that the reorganization of splicing factors we observed is the result of the inhibition of splicing in vivo.
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spelling pubmed-21199272008-05-01 Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors J Cell Biol Articles We have examined the functional significance of the organization of pre- mRNA splicing factors in a speckled distribution in the mammalian cell nucleus. Upon microinjection into living cells of oligonucleotides or antibodies that inhibit pre-mRNA splicing in vitro, we observed major changes in the organization of splicing factors in vivo. Interchromatin granule clusters became uniform in shape, decreased in number, and increased in both size and content of splicing factors, as measured by immunofluorescence. These changes were transient and the organization of splicing factors returned to their normal distribution by 24 h following microinjection. Microinjection of these oligonucleotides or antibodies also resulted in a reduction of transcription in vivo, but the oligonucleotides did not inhibit transcription in vitro. Control oligonucleotides did not disrupt splicing or transcription in vivo. We propose that the reorganization of splicing factors we observed is the result of the inhibition of splicing in vivo. The Rockefeller University Press 1994-02-01 /pmc/articles/PMC2119927/ /pubmed/8294510 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
Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title_full Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title_fullStr Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title_full_unstemmed Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title_short Disruption of pre-mRNA splicing in vivo results in reorganization of splicing factors
title_sort disruption of pre-mrna splicing in vivo results in reorganization of splicing factors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119927/
https://www.ncbi.nlm.nih.gov/pubmed/8294510