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Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities

TMPRSS6 (matriptase‐2) is a type II transmembrane serine protease involved in iron homoeostasis. At the cell surface of hepatocytes, TMPRSS6 cleaves haemojuvelin (HJV) and regulates the BMP/SMAD signalling pathway leading to production of hepcidin, a key regulator of iron absorption. Although four T...

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Autores principales: Dion, Sébastien P., Béliveau, François, Désilets, Antoine, Ghinet, Mariana Gabriela, Leduc, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867103/
https://www.ncbi.nlm.nih.gov/pubmed/29441715
http://dx.doi.org/10.1111/jcmm.13562
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author Dion, Sébastien P.
Béliveau, François
Désilets, Antoine
Ghinet, Mariana Gabriela
Leduc, Richard
author_facet Dion, Sébastien P.
Béliveau, François
Désilets, Antoine
Ghinet, Mariana Gabriela
Leduc, Richard
author_sort Dion, Sébastien P.
collection PubMed
description TMPRSS6 (matriptase‐2) is a type II transmembrane serine protease involved in iron homoeostasis. At the cell surface of hepatocytes, TMPRSS6 cleaves haemojuvelin (HJV) and regulates the BMP/SMAD signalling pathway leading to production of hepcidin, a key regulator of iron absorption. Although four TMPRSS6 human isoforms and three mice Tmprss6 isoforms are annotated in databases (Ensembl and RefSeq), their relative expression or activity has not been studied. Analyses of RNA‐seq data and RT‐PCR from human tissues reveal that TMPRSS6 isoform 1 (TMPRSS6‐1) and 3 are mostly expressed in human testis while TMPRSS6‐2 and TMPRSS6‐4 are the main transcripts expressed in human liver, testis and pituitary. Furthermore, we confirm the existence and analyse the relative expression of three annotated mice Tmprss6 isoforms. Using heterologous expression in HEK293 and Hep3B cells, we show that all human TMPRSS6 isoforms reach the cell surface but only TMPRSS6‐1 undergoes internalization. Moreover, truncated TMPRSS6‐3 or catalytically altered TMPRSS6‐4 interact with HJV and prevent its cleavage by TMPRSS6‐2, suggesting their potential role as dominant negative isoforms. Taken together, our results highlight the importance of understanding the precise function of each TMPRSS6 isoforms both in human and in mouse.
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spelling pubmed-58671032018-04-01 Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities Dion, Sébastien P. Béliveau, François Désilets, Antoine Ghinet, Mariana Gabriela Leduc, Richard J Cell Mol Med Original Articles TMPRSS6 (matriptase‐2) is a type II transmembrane serine protease involved in iron homoeostasis. At the cell surface of hepatocytes, TMPRSS6 cleaves haemojuvelin (HJV) and regulates the BMP/SMAD signalling pathway leading to production of hepcidin, a key regulator of iron absorption. Although four TMPRSS6 human isoforms and three mice Tmprss6 isoforms are annotated in databases (Ensembl and RefSeq), their relative expression or activity has not been studied. Analyses of RNA‐seq data and RT‐PCR from human tissues reveal that TMPRSS6 isoform 1 (TMPRSS6‐1) and 3 are mostly expressed in human testis while TMPRSS6‐2 and TMPRSS6‐4 are the main transcripts expressed in human liver, testis and pituitary. Furthermore, we confirm the existence and analyse the relative expression of three annotated mice Tmprss6 isoforms. Using heterologous expression in HEK293 and Hep3B cells, we show that all human TMPRSS6 isoforms reach the cell surface but only TMPRSS6‐1 undergoes internalization. Moreover, truncated TMPRSS6‐3 or catalytically altered TMPRSS6‐4 interact with HJV and prevent its cleavage by TMPRSS6‐2, suggesting their potential role as dominant negative isoforms. Taken together, our results highlight the importance of understanding the precise function of each TMPRSS6 isoforms both in human and in mouse. John Wiley and Sons Inc. 2018-02-14 2018-04 /pmc/articles/PMC5867103/ /pubmed/29441715 http://dx.doi.org/10.1111/jcmm.13562 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Dion, Sébastien P.
Béliveau, François
Désilets, Antoine
Ghinet, Mariana Gabriela
Leduc, Richard
Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title_full Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title_fullStr Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title_full_unstemmed Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title_short Transcriptome analysis reveals TMPRSS6 isoforms with distinct functionalities
title_sort transcriptome analysis reveals tmprss6 isoforms with distinct functionalities
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867103/
https://www.ncbi.nlm.nih.gov/pubmed/29441715
http://dx.doi.org/10.1111/jcmm.13562
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