Cellular localization and processing of primary transcripts of exonic microRNAs.

Processing of miRNAs occurs simultaneous with the transcription and splicing of their primary transcripts. For the small subset of exonic miRNAs it is unclear if the unspliced and/or spliced transcripts are used for miRNA biogenesis. We assessed endogenous levels and cellular location of primary tra...

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Autores principales: Izabella Slezak-Prochazka, Joost Kluiver, Debora de Jong, Gertrud Kortman, Nancy Halsema, Sibrand Poppema, Bart-Jan Kroesen, Anke van den Berg
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/e2874de8a1604f51aa25bdf687459001
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spelling oai:doaj.org-article:e2874de8a1604f51aa25bdf6874590012021-11-18T08:54:14ZCellular localization and processing of primary transcripts of exonic microRNAs.1932-620310.1371/journal.pone.0076647https://doaj.org/article/e2874de8a1604f51aa25bdf6874590012013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24073292/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Processing of miRNAs occurs simultaneous with the transcription and splicing of their primary transcripts. For the small subset of exonic miRNAs it is unclear if the unspliced and/or spliced transcripts are used for miRNA biogenesis. We assessed endogenous levels and cellular location of primary transcripts of three exonic miRNAs. The ratio between unspliced and spliced transcripts varied markedly, i.e. >1 for BIC, <1 for pri-miR-146a and variable for pri-miR-22. Endogenous unspliced transcripts were located almost exclusively in the nucleus and thus available for miRNA processing for all three miRNAs. Endogenous spliced pri-miRNA transcripts were present both in the nucleus and in the cytoplasm and thus only partly available for miRNA processing. Overexpression of constructs containing the 5' upstream exonic or intronic sequence flanking pre-miR-155 resulted in strongly enhanced miR-155 levels, indicating that the flanking sequence does not affect processing efficiency. Exogenously overexpressed full-length spliced BIC transcripts were present both in the nucleus and in the cytoplasm, were bound by the Microprocessor complex and resulted in enhanced miR-155 levels. We conclude that both unspliced and spliced transcripts of exonic miRNAs can be used for pre-miRNA cleavage. Splicing and cytoplasmic transport of spliced transcripts may present a mechanism to regulate levels of exonic microRNAs.Izabella Slezak-ProchazkaJoost KluiverDebora de JongGertrud KortmanNancy HalsemaSibrand PoppemaBart-Jan KroesenAnke van den BergPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 9, p e76647 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Izabella Slezak-Prochazka
Joost Kluiver
Debora de Jong
Gertrud Kortman
Nancy Halsema
Sibrand Poppema
Bart-Jan Kroesen
Anke van den Berg
Cellular localization and processing of primary transcripts of exonic microRNAs.
description Processing of miRNAs occurs simultaneous with the transcription and splicing of their primary transcripts. For the small subset of exonic miRNAs it is unclear if the unspliced and/or spliced transcripts are used for miRNA biogenesis. We assessed endogenous levels and cellular location of primary transcripts of three exonic miRNAs. The ratio between unspliced and spliced transcripts varied markedly, i.e. >1 for BIC, <1 for pri-miR-146a and variable for pri-miR-22. Endogenous unspliced transcripts were located almost exclusively in the nucleus and thus available for miRNA processing for all three miRNAs. Endogenous spliced pri-miRNA transcripts were present both in the nucleus and in the cytoplasm and thus only partly available for miRNA processing. Overexpression of constructs containing the 5' upstream exonic or intronic sequence flanking pre-miR-155 resulted in strongly enhanced miR-155 levels, indicating that the flanking sequence does not affect processing efficiency. Exogenously overexpressed full-length spliced BIC transcripts were present both in the nucleus and in the cytoplasm, were bound by the Microprocessor complex and resulted in enhanced miR-155 levels. We conclude that both unspliced and spliced transcripts of exonic miRNAs can be used for pre-miRNA cleavage. Splicing and cytoplasmic transport of spliced transcripts may present a mechanism to regulate levels of exonic microRNAs.
format article
author Izabella Slezak-Prochazka
Joost Kluiver
Debora de Jong
Gertrud Kortman
Nancy Halsema
Sibrand Poppema
Bart-Jan Kroesen
Anke van den Berg
author_facet Izabella Slezak-Prochazka
Joost Kluiver
Debora de Jong
Gertrud Kortman
Nancy Halsema
Sibrand Poppema
Bart-Jan Kroesen
Anke van den Berg
author_sort Izabella Slezak-Prochazka
title Cellular localization and processing of primary transcripts of exonic microRNAs.
title_short Cellular localization and processing of primary transcripts of exonic microRNAs.
title_full Cellular localization and processing of primary transcripts of exonic microRNAs.
title_fullStr Cellular localization and processing of primary transcripts of exonic microRNAs.
title_full_unstemmed Cellular localization and processing of primary transcripts of exonic microRNAs.
title_sort cellular localization and processing of primary transcripts of exonic micrornas.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/e2874de8a1604f51aa25bdf687459001
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