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spelling paper:paper_00278424_v94_n21_p11456_Cramer2023-06-08T14:54:36Z Functional association between promoter structure and transcript alternative splicing Fibronectin Transcription fibronectin rna polymerase ii alternative rna splicing article cell proliferation controlled study development gene structure hepatoma cell human human cell nonhuman priority journal promoter region rna transcription signal transduction spliceosome Alternative Splicing beta-Galactosidase Exons Fibronectins Globins Humans Models, Genetic Polymerase Chain Reaction Promoter Regions (Genetics) Recombinant Fusion Proteins RNA Polymerase II RNA Precursors RNA, Messenger Transcription, Genetic Transfection Tumor Cells, Cultured It has been assumed that constitutive and regulated splicing of RNA polymerase II transcripts depends exclusively on signals present in the RNA molecule. Here we show that changes in promoter structure strongly affect splice site selection. We investigated the splicing of the ED I exon, which encodes a facultative type III repeat of fibronectin, whose inclusion is regulated during development and in proliferative processes. We used an alternative splicing assay combined with promoter swapping to demonstrate that the extent of ED I splicing is dependent on the promoter structure from which the transcript originated and that this regulation is independent of the promoter strength. Thus, these results provide the first evidence for coupling between alternative splicing and promoter-specific transcription, which agrees with recent cytological and biochemical evidence of coordination between splicing and transcription. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00278424_v94_n21_p11456_Cramer http://hdl.handle.net/20.500.12110/paper_00278424_v94_n21_p11456_Cramer
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Fibronectin
Transcription
fibronectin
rna polymerase ii
alternative rna splicing
article
cell proliferation
controlled study
development
gene structure
hepatoma cell
human
human cell
nonhuman
priority journal
promoter region
rna transcription
signal transduction
spliceosome
Alternative Splicing
beta-Galactosidase
Exons
Fibronectins
Globins
Humans
Models, Genetic
Polymerase Chain Reaction
Promoter Regions (Genetics)
Recombinant Fusion Proteins
RNA Polymerase II
RNA Precursors
RNA, Messenger
Transcription, Genetic
Transfection
Tumor Cells, Cultured
spellingShingle Fibronectin
Transcription
fibronectin
rna polymerase ii
alternative rna splicing
article
cell proliferation
controlled study
development
gene structure
hepatoma cell
human
human cell
nonhuman
priority journal
promoter region
rna transcription
signal transduction
spliceosome
Alternative Splicing
beta-Galactosidase
Exons
Fibronectins
Globins
Humans
Models, Genetic
Polymerase Chain Reaction
Promoter Regions (Genetics)
Recombinant Fusion Proteins
RNA Polymerase II
RNA Precursors
RNA, Messenger
Transcription, Genetic
Transfection
Tumor Cells, Cultured
Functional association between promoter structure and transcript alternative splicing
topic_facet Fibronectin
Transcription
fibronectin
rna polymerase ii
alternative rna splicing
article
cell proliferation
controlled study
development
gene structure
hepatoma cell
human
human cell
nonhuman
priority journal
promoter region
rna transcription
signal transduction
spliceosome
Alternative Splicing
beta-Galactosidase
Exons
Fibronectins
Globins
Humans
Models, Genetic
Polymerase Chain Reaction
Promoter Regions (Genetics)
Recombinant Fusion Proteins
RNA Polymerase II
RNA Precursors
RNA, Messenger
Transcription, Genetic
Transfection
Tumor Cells, Cultured
description It has been assumed that constitutive and regulated splicing of RNA polymerase II transcripts depends exclusively on signals present in the RNA molecule. Here we show that changes in promoter structure strongly affect splice site selection. We investigated the splicing of the ED I exon, which encodes a facultative type III repeat of fibronectin, whose inclusion is regulated during development and in proliferative processes. We used an alternative splicing assay combined with promoter swapping to demonstrate that the extent of ED I splicing is dependent on the promoter structure from which the transcript originated and that this regulation is independent of the promoter strength. Thus, these results provide the first evidence for coupling between alternative splicing and promoter-specific transcription, which agrees with recent cytological and biochemical evidence of coordination between splicing and transcription.
title Functional association between promoter structure and transcript alternative splicing
title_short Functional association between promoter structure and transcript alternative splicing
title_full Functional association between promoter structure and transcript alternative splicing
title_fullStr Functional association between promoter structure and transcript alternative splicing
title_full_unstemmed Functional association between promoter structure and transcript alternative splicing
title_sort functional association between promoter structure and transcript alternative splicing
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00278424_v94_n21_p11456_Cramer
http://hdl.handle.net/20.500.12110/paper_00278424_v94_n21_p11456_Cramer
_version_ 1768542825134161920