Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region

OBJECTIVE - Tissue factor pathway inhibitor (TFPI) blocks the initiation of coagulation by inhibiting TF-activated factor VII, activated factor X, and early prothrombinase. Humans produce two 3' splice variants, TFPIa and TFPIß, which are differentially expressed in endothelial cells and platel...

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Main Authors: Ellery, Paul, Maroney, S., Martinez, N., Wickens, M., Mast, A.
Format: Journal Article
Published: 2014
Online Access:http://hdl.handle.net/20.500.11937/20499
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author Ellery, Paul
Maroney, S.
Martinez, N.
Wickens, M.
Mast, A.
author_facet Ellery, Paul
Maroney, S.
Martinez, N.
Wickens, M.
Mast, A.
author_sort Ellery, Paul
building Curtin Institutional Repository
collection Online Access
description OBJECTIVE - Tissue factor pathway inhibitor (TFPI) blocks the initiation of coagulation by inhibiting TF-activated factor VII, activated factor X, and early prothrombinase. Humans produce two 3' splice variants, TFPIa and TFPIß, which are differentially expressed in endothelial cells and platelets and possess distinct structural features affecting their inhibitory function. TFPI also undergoes alternative splicing of exon 2 within its 5' untranslated region. The role of exon 2 splicing in translational regulation of human TFPI isoform expression is investigated. APPROACH AND RESULTS - Exon 2 splicing occurs in TFPIa and TFPIß transcripts. Human tissue mRNA analysis uncovered a wide variability of exon 2 expression. Polysome analysis revealed a repressive effect of exon 2 on TFPIß translation but not on TFPIa. Luciferase reporter assays further exposed strong translational repression of TFPIß (90%) but not TFPIa. Use of a Morpholino to remove exon 2 from TFPI mRNA increased cell surface expression of endogenous TFPIß. Exon 2 also repressed luciferase production (80% to 90%) when paired with the ß-actin 3' untranslated region, suggesting that it is a general translational negative element whose effects are overcome by the TFPIa 3' untranslated region. CONCLUSIONS - Exon 2 is a molecular switch that prevents translation of TFPIß. This is the first demonstration of a 5' untranslated region alternative splicing event that alters translation of isoforms produced via independent 3' splicing events within the same gene. Therefore, it represents a previously unrecognized mechanism for translational control of protein expression. Differential expression of exon 2 denotes a mechanism to provide temporal and tissue-specific regulation of TFPIß-mediated anticoagulant activity. © 2013 American Heart Association, Inc.
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spelling curtin-20.500.11937-204992017-09-13T13:50:23Z Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region Ellery, Paul Maroney, S. Martinez, N. Wickens, M. Mast, A. OBJECTIVE - Tissue factor pathway inhibitor (TFPI) blocks the initiation of coagulation by inhibiting TF-activated factor VII, activated factor X, and early prothrombinase. Humans produce two 3' splice variants, TFPIa and TFPIß, which are differentially expressed in endothelial cells and platelets and possess distinct structural features affecting their inhibitory function. TFPI also undergoes alternative splicing of exon 2 within its 5' untranslated region. The role of exon 2 splicing in translational regulation of human TFPI isoform expression is investigated. APPROACH AND RESULTS - Exon 2 splicing occurs in TFPIa and TFPIß transcripts. Human tissue mRNA analysis uncovered a wide variability of exon 2 expression. Polysome analysis revealed a repressive effect of exon 2 on TFPIß translation but not on TFPIa. Luciferase reporter assays further exposed strong translational repression of TFPIß (90%) but not TFPIa. Use of a Morpholino to remove exon 2 from TFPI mRNA increased cell surface expression of endogenous TFPIß. Exon 2 also repressed luciferase production (80% to 90%) when paired with the ß-actin 3' untranslated region, suggesting that it is a general translational negative element whose effects are overcome by the TFPIa 3' untranslated region. CONCLUSIONS - Exon 2 is a molecular switch that prevents translation of TFPIß. This is the first demonstration of a 5' untranslated region alternative splicing event that alters translation of isoforms produced via independent 3' splicing events within the same gene. Therefore, it represents a previously unrecognized mechanism for translational control of protein expression. Differential expression of exon 2 denotes a mechanism to provide temporal and tissue-specific regulation of TFPIß-mediated anticoagulant activity. © 2013 American Heart Association, Inc. 2014 Journal Article http://hdl.handle.net/20.500.11937/20499 10.1161/ATVBAHA.113.302660 unknown
spellingShingle Ellery, Paul
Maroney, S.
Martinez, N.
Wickens, M.
Mast, A.
Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title_full Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title_fullStr Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title_full_unstemmed Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title_short Translation of human tissue factor pathway inhibitor-ß mRNA is controlled by alternative splicing within the 5' untranslated region
title_sort translation of human tissue factor pathway inhibitor-ß mrna is controlled by alternative splicing within the 5' untranslated region
url http://hdl.handle.net/20.500.11937/20499