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Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans
In mammals, tropomyosin is encoded by four known TPM genes (TPM1, TPM2, TPM3, and TPM4) each of which can generate a number of TPM isoforms via alternative splicing and/or using alternate promoters. In humans, the sarcomeric isoform(s) of each of the TPM genes, except for the TPM4, have been known f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040813/ https://www.ncbi.nlm.nih.gov/pubmed/27703814 http://dx.doi.org/10.1155/2016/3105478 |
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author | Dube, Dipak K. Dube, Syamalima Abbott, Lynn Alshiekh-Nasany, Ruham Mitschow, Charles Poiesz, Bernard J. |
author_facet | Dube, Dipak K. Dube, Syamalima Abbott, Lynn Alshiekh-Nasany, Ruham Mitschow, Charles Poiesz, Bernard J. |
author_sort | Dube, Dipak K. |
collection | PubMed |
description | In mammals, tropomyosin is encoded by four known TPM genes (TPM1, TPM2, TPM3, and TPM4) each of which can generate a number of TPM isoforms via alternative splicing and/or using alternate promoters. In humans, the sarcomeric isoform(s) of each of the TPM genes, except for the TPM4, have been known for a long time. Recently, on the basis of computational analyses of the human genome sequence, the predicted sequence of TPM4α has been posted in GenBank. We designed primer-pairs for RT-PCR and showed the expression of the transcripts of TPM4α and a novel isoform TPM4δ in human heart and skeletal muscle. qRT-PCR shows that the relative expression of TPM4α and TPM4δ is higher in human cardiac muscle. Western blot analyses using CH1 monoclonal antibodies show the absence of the expression of TPM4δ protein (~28 kDa) in human heart muscle. 2D western blot analyses with the same antibody show the expression of at least nine distinct tropomyosin molecules with a mass ~32 kD and above in adult heart. By Mass spectrometry, we determined the amino acid sequences of the extracted proteins from these spots. Spot “G” reveals the putative expression of TPM4α along with TPM1α protein in human adult heart. |
format | Online Article Text |
id | pubmed-5040813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50408132016-10-04 Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans Dube, Dipak K. Dube, Syamalima Abbott, Lynn Alshiekh-Nasany, Ruham Mitschow, Charles Poiesz, Bernard J. Mol Biol Int Research Article In mammals, tropomyosin is encoded by four known TPM genes (TPM1, TPM2, TPM3, and TPM4) each of which can generate a number of TPM isoforms via alternative splicing and/or using alternate promoters. In humans, the sarcomeric isoform(s) of each of the TPM genes, except for the TPM4, have been known for a long time. Recently, on the basis of computational analyses of the human genome sequence, the predicted sequence of TPM4α has been posted in GenBank. We designed primer-pairs for RT-PCR and showed the expression of the transcripts of TPM4α and a novel isoform TPM4δ in human heart and skeletal muscle. qRT-PCR shows that the relative expression of TPM4α and TPM4δ is higher in human cardiac muscle. Western blot analyses using CH1 monoclonal antibodies show the absence of the expression of TPM4δ protein (~28 kDa) in human heart muscle. 2D western blot analyses with the same antibody show the expression of at least nine distinct tropomyosin molecules with a mass ~32 kD and above in adult heart. By Mass spectrometry, we determined the amino acid sequences of the extracted proteins from these spots. Spot “G” reveals the putative expression of TPM4α along with TPM1α protein in human adult heart. Hindawi Publishing Corporation 2016 2016-09-15 /pmc/articles/PMC5040813/ /pubmed/27703814 http://dx.doi.org/10.1155/2016/3105478 Text en Copyright © 2016 Dipak K. Dube et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dube, Dipak K. Dube, Syamalima Abbott, Lynn Alshiekh-Nasany, Ruham Mitschow, Charles Poiesz, Bernard J. Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title | Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title_full | Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title_fullStr | Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title_full_unstemmed | Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title_short | Cloning, Sequencing, and the Expression of the Elusive Sarcomeric TPM4α Isoform in Humans |
title_sort | cloning, sequencing, and the expression of the elusive sarcomeric tpm4α isoform in humans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040813/ https://www.ncbi.nlm.nih.gov/pubmed/27703814 http://dx.doi.org/10.1155/2016/3105478 |
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