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Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation

Nebulin is a very large protein required for assembly of the contractile machinery in muscle. Mutations in the nebulin gene NEB are a common cause of nemaline myopathy. Nebulin mRNA is alternatively-spliced so that each mRNA contains either exon 143 or exon 144. We have produced monoclonal antibodie...

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Autores principales: Lam, Le Thanh, Holt, Ian, Laitila, Jenni, Hanif, Mubashir, Pelin, Katarina, Wallgren-Pettersson, Carina, Sewry, Caroline A., Morris, Glenn E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200726/
https://www.ncbi.nlm.nih.gov/pubmed/30356055
http://dx.doi.org/10.1038/s41598-018-33281-6
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author Lam, Le Thanh
Holt, Ian
Laitila, Jenni
Hanif, Mubashir
Pelin, Katarina
Wallgren-Pettersson, Carina
Sewry, Caroline A.
Morris, Glenn E.
author_facet Lam, Le Thanh
Holt, Ian
Laitila, Jenni
Hanif, Mubashir
Pelin, Katarina
Wallgren-Pettersson, Carina
Sewry, Caroline A.
Morris, Glenn E.
author_sort Lam, Le Thanh
collection PubMed
description Nebulin is a very large protein required for assembly of the contractile machinery in muscle. Mutations in the nebulin gene NEB are a common cause of nemaline myopathy. Nebulin mRNA is alternatively-spliced so that each mRNA contains either exon 143 or exon 144. We have produced monoclonal antibodies specific for the regions of nebulin encoded by these two exons, enabling analysis of expression of isoforms at the protein level for the first time. All antibodies recognized a protein of the expected size (600–900 kD) and stained cross-striations of sarcomeres in muscle sections. Expression of exon 143 is developmentally-regulated since newly-formed myotubes in cell culture expressed nebulin with exon 144 only; this was confirmed at the mRNA level by qPCR. In fetal muscle, nebulin with exon 143 was expressed in some myotubes by 12-weeks of gestation and strongly-expressed in most myotubes by 17-weeks. In mature human muscle, the exon 144 antibody stained all fibres, but the exon 143 antibody staining varied from very strong in some fibres to almost-undetectable in other fibres. The results show that nebulin containing exon 144 is the default isoform early in myogenesis, while regulated expression of nebulin containing exon 143 occurs at later stages of muscle development.
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spelling pubmed-62007262018-10-25 Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation Lam, Le Thanh Holt, Ian Laitila, Jenni Hanif, Mubashir Pelin, Katarina Wallgren-Pettersson, Carina Sewry, Caroline A. Morris, Glenn E. Sci Rep Article Nebulin is a very large protein required for assembly of the contractile machinery in muscle. Mutations in the nebulin gene NEB are a common cause of nemaline myopathy. Nebulin mRNA is alternatively-spliced so that each mRNA contains either exon 143 or exon 144. We have produced monoclonal antibodies specific for the regions of nebulin encoded by these two exons, enabling analysis of expression of isoforms at the protein level for the first time. All antibodies recognized a protein of the expected size (600–900 kD) and stained cross-striations of sarcomeres in muscle sections. Expression of exon 143 is developmentally-regulated since newly-formed myotubes in cell culture expressed nebulin with exon 144 only; this was confirmed at the mRNA level by qPCR. In fetal muscle, nebulin with exon 143 was expressed in some myotubes by 12-weeks of gestation and strongly-expressed in most myotubes by 17-weeks. In mature human muscle, the exon 144 antibody stained all fibres, but the exon 143 antibody staining varied from very strong in some fibres to almost-undetectable in other fibres. The results show that nebulin containing exon 144 is the default isoform early in myogenesis, while regulated expression of nebulin containing exon 143 occurs at later stages of muscle development. Nature Publishing Group UK 2018-10-24 /pmc/articles/PMC6200726/ /pubmed/30356055 http://dx.doi.org/10.1038/s41598-018-33281-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lam, Le Thanh
Holt, Ian
Laitila, Jenni
Hanif, Mubashir
Pelin, Katarina
Wallgren-Pettersson, Carina
Sewry, Caroline A.
Morris, Glenn E.
Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title_full Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title_fullStr Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title_full_unstemmed Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title_short Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
title_sort two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200726/
https://www.ncbi.nlm.nih.gov/pubmed/30356055
http://dx.doi.org/10.1038/s41598-018-33281-6
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