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Expression of various sarcomeric tropomyosin isoforms in equine striated muscles
In order to better understand the training and athletic activity of horses, we must have complete understanding of the isoform diversity of various myofibrillar protein genes like tropomyosin. Tropomyosin (TPM), a coiled-coil dimeric protein, is a component of thin filament in striated muscles. In m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of Veterinary Medicine, University of Tripoli and Libyan Authority for Research, Science and Technology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498770/ https://www.ncbi.nlm.nih.gov/pubmed/28717602 http://dx.doi.org/10.4314/ovj.v7i2.17 |
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author | Dube, Syamalima Chionuma, Henry Matoq, Amr Alshiekh-Nasany, Ruham Abbott, Lynn Poiesz, Bernard J. Dube, Dipak K. |
author_facet | Dube, Syamalima Chionuma, Henry Matoq, Amr Alshiekh-Nasany, Ruham Abbott, Lynn Poiesz, Bernard J. Dube, Dipak K. |
author_sort | Dube, Syamalima |
collection | PubMed |
description | In order to better understand the training and athletic activity of horses, we must have complete understanding of the isoform diversity of various myofibrillar protein genes like tropomyosin. Tropomyosin (TPM), a coiled-coil dimeric protein, is a component of thin filament in striated muscles. In mammals, four TPM genes (TPM1, TPM2, TPM3, and TPM4) generate a multitude of TPM isoforms via alternate splicing and/or using different promoters. Unfortunately, our knowledge of TPM isoform diversity in the horse is very limited. Hence, we undertook a comprehensive exploratory study of various TPM isoforms from horse heart and skeletal muscle. We have cloned and sequenced two sarcomeric isoforms of the TPM1 gene called TPM1α and TPM1κ, one sarcomeric isoform of the TPM2 and one of the TPM3 gene, TPM2α and TPM3α respectively. By qRT-PCR using both relative expression and copy number, we have shown that TPM1α expression compared to TPM1κ is very high in heart. On the other hand, the expression of TPM1α is higher in skeletal muscle compared to heart. Further, the expression of TPM2α and TPM3α are higher in skeletal muscle compared to heart. Using western blot analyses with CH1 monoclonal antibody we have shown the high expression levels of sarcomeric TPM proteins in cardiac and skeletal muscle. Due to the paucity of isoform specific antibodies we cannot specifically detect the expression of TPM1κ in horse striated muscle. To the best of our knowledge this is the very first report on the characterization of sarcmeric TPMs in horse striated muscle. |
format | Online Article Text |
id | pubmed-5498770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Faculty of Veterinary Medicine, University of Tripoli and Libyan Authority for Research, Science and Technology |
record_format | MEDLINE/PubMed |
spelling | pubmed-54987702017-07-17 Expression of various sarcomeric tropomyosin isoforms in equine striated muscles Dube, Syamalima Chionuma, Henry Matoq, Amr Alshiekh-Nasany, Ruham Abbott, Lynn Poiesz, Bernard J. Dube, Dipak K. Open Vet J Original Article In order to better understand the training and athletic activity of horses, we must have complete understanding of the isoform diversity of various myofibrillar protein genes like tropomyosin. Tropomyosin (TPM), a coiled-coil dimeric protein, is a component of thin filament in striated muscles. In mammals, four TPM genes (TPM1, TPM2, TPM3, and TPM4) generate a multitude of TPM isoforms via alternate splicing and/or using different promoters. Unfortunately, our knowledge of TPM isoform diversity in the horse is very limited. Hence, we undertook a comprehensive exploratory study of various TPM isoforms from horse heart and skeletal muscle. We have cloned and sequenced two sarcomeric isoforms of the TPM1 gene called TPM1α and TPM1κ, one sarcomeric isoform of the TPM2 and one of the TPM3 gene, TPM2α and TPM3α respectively. By qRT-PCR using both relative expression and copy number, we have shown that TPM1α expression compared to TPM1κ is very high in heart. On the other hand, the expression of TPM1α is higher in skeletal muscle compared to heart. Further, the expression of TPM2α and TPM3α are higher in skeletal muscle compared to heart. Using western blot analyses with CH1 monoclonal antibody we have shown the high expression levels of sarcomeric TPM proteins in cardiac and skeletal muscle. Due to the paucity of isoform specific antibodies we cannot specifically detect the expression of TPM1κ in horse striated muscle. To the best of our knowledge this is the very first report on the characterization of sarcmeric TPMs in horse striated muscle. Faculty of Veterinary Medicine, University of Tripoli and Libyan Authority for Research, Science and Technology 2017 2017-06-26 /pmc/articles/PMC5498770/ /pubmed/28717602 http://dx.doi.org/10.4314/ovj.v7i2.17 Text en Copyright: © Open Veterinary Journal http://creativecommons.org/licenses/by-nc-sa/4.0 Open Veterinary Journal is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Original Article Dube, Syamalima Chionuma, Henry Matoq, Amr Alshiekh-Nasany, Ruham Abbott, Lynn Poiesz, Bernard J. Dube, Dipak K. Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title | Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title_full | Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title_fullStr | Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title_full_unstemmed | Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title_short | Expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
title_sort | expression of various sarcomeric tropomyosin isoforms in equine striated muscles |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498770/ https://www.ncbi.nlm.nih.gov/pubmed/28717602 http://dx.doi.org/10.4314/ovj.v7i2.17 |
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