Coupling between transcription and alternative splicing

The scenario of alternative splicing regulation is far more complex than the classical picture of a pre-mRNA being processed post-transcriptionally in more than one way. Introns are efficiently removed while transcripts are still being synthesized, supporting the idea of a co-transcriptional regulat...

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Publicado: 2013
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09273042_v_n_p1_Schor
http://hdl.handle.net/20.500.12110/paper_09273042_v_n_p1_Schor
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spelling paper:paper_09273042_v_n_p1_Schor2023-06-08T15:51:50Z Coupling between transcription and alternative splicing Alternative splicing Chromatin Co-transcriptional splicing Kinetic model RNA polymerase II-CTD Transcription-splicing coupling messenger RNA RNA polymerase II alternative RNA splicing article carcinogenesis chromatin structure genetic transcription human intron kinetics priority journal protein assembly regulatory mechanism RNA transcription spliceosome transcription regulation The scenario of alternative splicing regulation is far more complex than the classical picture of a pre-mRNA being processed post-transcriptionally in more than one way. Introns are efficiently removed while transcripts are still being synthesized, supporting the idea of a co-transcriptional regulation of alternative splicing. Evidence of a functional coupling between splicing and transcription has recently emerged as it was observed that properties of one process may affect the outcome of the other. Co-transcriptionality is thought to improve splicing efficiency and kinetics by directing the nascent pre-mRNA into proper spliceosome assembly and favoring splicing factor recruitment. Two models have been proposed to explain the coupling of transcription and alternative splicing: in the recruitment model, promoters and pol II status affect the recruitment to the transcribing gene of splicing factors or bifunctional factors acting on both transcription and splicing; in the kinetic model, differences in the elongation rate of pol II would determine the timing in which splicing sites are presented, and thus the outcome of alternative splicing decisions. In the later model, chromatin structure has emerged as a key regulator. Although definitive evidence for transcriptionally coupled alternative splicing alterations in tumor development or cancer pathogenesis is still missing, many alternative splicing events altered in cancer might be subject to transcription-splicing coupling regulation. © 2013 Springer-Verlag Berlin Heidelberg. 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09273042_v_n_p1_Schor http://hdl.handle.net/20.500.12110/paper_09273042_v_n_p1_Schor
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Alternative splicing
Chromatin
Co-transcriptional splicing
Kinetic model
RNA polymerase II-CTD
Transcription-splicing coupling
messenger RNA
RNA polymerase II
alternative RNA splicing
article
carcinogenesis
chromatin structure
genetic transcription
human
intron
kinetics
priority journal
protein assembly
regulatory mechanism
RNA transcription
spliceosome
transcription regulation
spellingShingle Alternative splicing
Chromatin
Co-transcriptional splicing
Kinetic model
RNA polymerase II-CTD
Transcription-splicing coupling
messenger RNA
RNA polymerase II
alternative RNA splicing
article
carcinogenesis
chromatin structure
genetic transcription
human
intron
kinetics
priority journal
protein assembly
regulatory mechanism
RNA transcription
spliceosome
transcription regulation
Coupling between transcription and alternative splicing
topic_facet Alternative splicing
Chromatin
Co-transcriptional splicing
Kinetic model
RNA polymerase II-CTD
Transcription-splicing coupling
messenger RNA
RNA polymerase II
alternative RNA splicing
article
carcinogenesis
chromatin structure
genetic transcription
human
intron
kinetics
priority journal
protein assembly
regulatory mechanism
RNA transcription
spliceosome
transcription regulation
description The scenario of alternative splicing regulation is far more complex than the classical picture of a pre-mRNA being processed post-transcriptionally in more than one way. Introns are efficiently removed while transcripts are still being synthesized, supporting the idea of a co-transcriptional regulation of alternative splicing. Evidence of a functional coupling between splicing and transcription has recently emerged as it was observed that properties of one process may affect the outcome of the other. Co-transcriptionality is thought to improve splicing efficiency and kinetics by directing the nascent pre-mRNA into proper spliceosome assembly and favoring splicing factor recruitment. Two models have been proposed to explain the coupling of transcription and alternative splicing: in the recruitment model, promoters and pol II status affect the recruitment to the transcribing gene of splicing factors or bifunctional factors acting on both transcription and splicing; in the kinetic model, differences in the elongation rate of pol II would determine the timing in which splicing sites are presented, and thus the outcome of alternative splicing decisions. In the later model, chromatin structure has emerged as a key regulator. Although definitive evidence for transcriptionally coupled alternative splicing alterations in tumor development or cancer pathogenesis is still missing, many alternative splicing events altered in cancer might be subject to transcription-splicing coupling regulation. © 2013 Springer-Verlag Berlin Heidelberg.
title Coupling between transcription and alternative splicing
title_short Coupling between transcription and alternative splicing
title_full Coupling between transcription and alternative splicing
title_fullStr Coupling between transcription and alternative splicing
title_full_unstemmed Coupling between transcription and alternative splicing
title_sort coupling between transcription and alternative splicing
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09273042_v_n_p1_Schor
http://hdl.handle.net/20.500.12110/paper_09273042_v_n_p1_Schor
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