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Extremely fast and incredibly close: cotranscriptional splicing in budding yeast

RNA splicing, an essential part of eukaryotic pre-messenger RNA processing, can be simultaneous with transcription by RNA polymerase II. Here, we compare and review independent next-generation sequencing methods that jointly quantify transcription and splicing in budding yeast. For many yeast transc...

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Detalles Bibliográficos
Autores principales: Wallace, Edward W.J., Beggs, Jean D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393171/
https://www.ncbi.nlm.nih.gov/pubmed/28153948
http://dx.doi.org/10.1261/rna.060830.117
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author Wallace, Edward W.J.
Beggs, Jean D.
author_facet Wallace, Edward W.J.
Beggs, Jean D.
author_sort Wallace, Edward W.J.
collection PubMed
description RNA splicing, an essential part of eukaryotic pre-messenger RNA processing, can be simultaneous with transcription by RNA polymerase II. Here, we compare and review independent next-generation sequencing methods that jointly quantify transcription and splicing in budding yeast. For many yeast transcripts, splicing is fast, taking place within seconds of intron transcription, while polymerase is within a few dozens of nucleotides of the 3′ splice site. Ribosomal protein transcripts are spliced particularly fast and cotranscriptionally. However, some transcripts are spliced inefficiently or mainly post-transcriptionally. Intron-mediated regulation of some genes is likely to be cotranscriptional. We suggest that intermediates of the splicing reaction, missing from current data sets, may hold key information about splicing kinetics.
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spelling pubmed-53931712017-05-02 Extremely fast and incredibly close: cotranscriptional splicing in budding yeast Wallace, Edward W.J. Beggs, Jean D. RNA Mini-Review RNA splicing, an essential part of eukaryotic pre-messenger RNA processing, can be simultaneous with transcription by RNA polymerase II. Here, we compare and review independent next-generation sequencing methods that jointly quantify transcription and splicing in budding yeast. For many yeast transcripts, splicing is fast, taking place within seconds of intron transcription, while polymerase is within a few dozens of nucleotides of the 3′ splice site. Ribosomal protein transcripts are spliced particularly fast and cotranscriptionally. However, some transcripts are spliced inefficiently or mainly post-transcriptionally. Intron-mediated regulation of some genes is likely to be cotranscriptional. We suggest that intermediates of the splicing reaction, missing from current data sets, may hold key information about splicing kinetics. Cold Spring Harbor Laboratory Press 2017-05 /pmc/articles/PMC5393171/ /pubmed/28153948 http://dx.doi.org/10.1261/rna.060830.117 Text en © 2017 Wallace and Beggs; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Mini-Review
Wallace, Edward W.J.
Beggs, Jean D.
Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title_full Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title_fullStr Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title_full_unstemmed Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title_short Extremely fast and incredibly close: cotranscriptional splicing in budding yeast
title_sort extremely fast and incredibly close: cotranscriptional splicing in budding yeast
topic Mini-Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393171/
https://www.ncbi.nlm.nih.gov/pubmed/28153948
http://dx.doi.org/10.1261/rna.060830.117
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