Writing a wrong: Coupled RNA polymerase II transcription and RNA quality control

Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3′ end processing of different RNA species to help ensure quality control of the transcriptome. Many imprope...

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Published in:Wiley interdisciplinary reviews. RNA Vol. 10; no. 4; pp. e1529 - n/a
Main Authors: Peck, Sarah A., Hughes, Katlyn D., Victorino, Jose F., Mosley, Amber L.
Format: Journal Article
Language:English
Published: Hoboken, USA John Wiley & Sons, Inc 01-07-2019
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Abstract Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3′ end processing of different RNA species to help ensure quality control of the transcriptome. Many improperly processed transcripts are not exported from the nucleus, are restricted to the site of transcription, and are in some cases degraded, which helps to limit any possibility of aberrant RNA causing harm to cellular health. These critical quality control pathways are regulated by the highly dynamic protein–protein interaction network at the site of transcription. Recent work has further revealed the extent to which the processes of transcription and RNA processing and quality control are integrated, and how critically their coupling relies upon the dynamic protein interactions that take place co‐transcriptionally. This review focuses specifically on the intricate balance between 3′ end processing and RNA decay during transcription termination. This article is categorized under: RNA Turnover and Surveillance > Turnover/Surveillance Mechanisms RNA Processing > 3' End Processing RNA Processing > Splicing Mechanisms RNA Processing > Capping and 5' End Modifications Dynamic coupling of RNAPII transcription complex and RNA processing machinery is the first‐line of defense for nuclear RNA quality control.
AbstractList Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3′ end processing of different RNA species to help ensure quality control of the transcriptome. Many improperly processed transcripts are not exported from the nucleus, are restricted to the site of transcription, and are in some cases degraded, which helps to limit any possibility of aberrant RNA causing harm to cellular health. These critical quality control pathways are regulated by the highly dynamic protein–protein interaction network at the site of transcription. Recent work has further revealed the extent to which the processes of transcription and RNA processing and quality control are integrated, and how critically their coupling relies upon the dynamic protein interactions that take place co‐transcriptionally. This review focuses specifically on the intricate balance between 3′ end processing and RNA decay during transcription termination. This article is categorized under: RNA Turnover and Surveillance > Turnover/Surveillance Mechanisms RNA Processing > 3' End Processing RNA Processing > Splicing Mechanisms RNA Processing > Capping and 5' End Modifications Dynamic coupling of RNAPII transcription complex and RNA processing machinery is the first‐line of defense for nuclear RNA quality control.
Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3′ end processing of different RNA species to help ensure quality control of the transcriptome. Many improperly processed transcripts are not exported from the nucleus, are restricted to the site of transcription, and are in some cases degraded, which helps to limit any possibility of aberrant RNA causing harm to cellular health. These critical quality control pathways are regulated by the highly dynamic protein–protein interaction network at the site of transcription. Recent work has further revealed the extent to which the processes of transcription and RNA processing and quality control are integrated, and how critically their coupling relies upon the dynamic protein interactions that take place co‐transcriptionally. This review focuses specifically on the intricate balance between 3′ end processing and RNA decay during transcription termination. This article is categorized under: RNA Turnover and Surveillance > Turnover/Surveillance Mechanisms RNA Processing > 3' End Processing RNA Processing > Splicing Mechanisms RNA Processing > Capping and 5' End Modifications
Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co-transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3' end processing of different RNA species to help ensure quality control of the transcriptome. Many improperly processed transcripts are not exported from the nucleus, are restricted to the site of transcription, and are in some cases degraded, which helps to limit any possibility of aberrant RNA causing harm to cellular health. These critical quality control pathways are regulated by the highly dynamic protein-protein interaction network at the site of transcription. Recent work has further revealed the extent to which the processes of transcription and RNA processing and quality control are integrated, and how critically their coupling relies upon the dynamic protein interactions that take place co-transcriptionally. This review focuses specifically on the intricate balance between 3' end processing and RNA decay during transcription termination. This article is categorized under: RNA Turnover and Surveillance > Turnover/Surveillance Mechanisms RNA Processing > 3' End Processing RNA Processing > Splicing Mechanisms RNA Processing > Capping and 5' End Modifications.
Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient and proper capping, splicing, and 3′ end processing of different RNA species to help ensure quality control of the transcriptome. Many improperly processed transcripts are not exported from the nucleus, are restricted to the site of transcription, and are in some cases degraded, which helps to limit any possibility of aberrant RNA causing harm to cellular health. These critical quality control pathways are regulated by the highly dynamic protein–protein interaction network at the site of transcription. Recent work has further revealed the extent to which the processes of transcription and RNA processing and quality control are integrated, and how critically their coupling relies upon the dynamic protein interactions that take place co‐transcriptionally. This review focuses specifically on the intricate balance between 3′ end processing and RNA decay during transcription termination.This article is categorized under:RNA Turnover and Surveillance > Turnover/Surveillance MechanismsRNA Processing > 3' End ProcessingRNA Processing > Splicing MechanismsRNA Processing > Capping and 5' End Modifications
Author Victorino, Jose F.
Hughes, Katlyn D.
Mosley, Amber L.
Peck, Sarah A.
AuthorAffiliation 1 Department of Biochemistry and Molecular Biology Indiana University School of Medicine Indianapolis Indiana
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  surname: Mosley
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30848101$$D View this record in MEDLINE/PubMed
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O66
O9-
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WHWMO
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CGR
CUY
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Wed Jul 24 14:45:44 EDT 2024
Tue Nov 19 04:56:25 EST 2024
Fri Nov 22 00:04:03 EST 2024
Sat Sep 28 08:27:17 EDT 2024
Sat Aug 24 01:14:40 EDT 2024
IsDoiOpenAccess true
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Issue 4
Keywords termination
co-transcriptional
quality control
transcription
3′ end processing
capping
splicing
RNA processing
RNAPII
Language English
License Attribution-NonCommercial
2019 The Authors. WIREs RNA published by Wiley Periodicals, Inc.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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MergedId FETCHMERGED-LOGICAL-c5099-c8466dfab37a60fb3831748ad189b04527e8207dfdcc7418853ca3b9a40d84e33
Notes Funding information
National Heart and Lung Institute, Grant/Award Number: T32 HL007910; National Institute of General Medical Sciences, Grant/Award Number: GM099714; National Science Foundation, Grant/Award Number: MCB 1515748
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-2
The copyright line for this article was changed on 18 March 2019 after original online publication.
Funding information National Heart and Lung Institute, Grant/Award Number: T32 HL007910; National Institute of General Medical Sciences, Grant/Award Number: GM099714; National Science Foundation, Grant/Award Number: MCB 1515748
OpenAccessLink https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fwrna.1529
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PublicationTitle Wiley interdisciplinary reviews. RNA
PublicationTitleAlternate Wiley Interdiscip Rev RNA
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Publisher John Wiley & Sons, Inc
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Snippet Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co‐transcriptional RNA processing helps to ensure efficient...
Processing and maturation of precursor RNA species is coupled to RNA polymerase II transcription. Co-transcriptional RNA processing helps to ensure efficient...
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SubjectTerms 3′ end processing
Advanced Review
Advanced Reviews
capping
co‐transcriptional
DNA-directed RNA polymerase
End Modifications
Gene expression
Protein interaction
Protein Interaction Maps
Proteins
Quality control
RNA polymerase
RNA Polymerase II - metabolism
RNA Precursors - metabolism
RNA processing
RNA Processing, Post-Transcriptional
RNA, Messenger - metabolism
RNAPII
Splicing
Splicing Mechanisms
Surveillance
termination
transcription
Transcription termination
Transcription, Genetic
Turnover/Surveillance Mechanisms
Title Writing a wrong: Coupled RNA polymerase II transcription and RNA quality control
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fwrna.1529
https://www.ncbi.nlm.nih.gov/pubmed/30848101
https://www.proquest.com/docview/2239621698
https://search.proquest.com/docview/2189538951
https://pubmed.ncbi.nlm.nih.gov/PMC6570551
Volume 10
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