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...

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Veröffentlicht in:Nature communications 2010-10, Vol.1 (1), p.97-97, Article 97
Hauptverfasser: Dias, Anusha P., Dufu, Kobina, Lei, Haixin, Reed, Robin
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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
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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. 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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
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