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Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene

The Duchenne muscular dystrophy (DMD) gene is one of the largest genes in the human genome. The gene exhibits a complex arrangement of seven alternative promoters, which drive the expression of three full length and four shorter isoforms. Dp116, the second smallest product of the DMD gene, is a Schw...

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Autores principales: Matsuo, Masafumi, Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Kawaguchi, Tatsuya, Zhang, Zhujun, Nishio, Hisahide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664101/
https://www.ncbi.nlm.nih.gov/pubmed/28974057
http://dx.doi.org/10.3390/genes8100251
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author Matsuo, Masafumi
Awano, Hiroyuki
Matsumoto, Masaaki
Nagai, Masashi
Kawaguchi, Tatsuya
Zhang, Zhujun
Nishio, Hisahide
author_facet Matsuo, Masafumi
Awano, Hiroyuki
Matsumoto, Masaaki
Nagai, Masashi
Kawaguchi, Tatsuya
Zhang, Zhujun
Nishio, Hisahide
author_sort Matsuo, Masafumi
collection PubMed
description The Duchenne muscular dystrophy (DMD) gene is one of the largest genes in the human genome. The gene exhibits a complex arrangement of seven alternative promoters, which drive the expression of three full length and four shorter isoforms. Dp116, the second smallest product of the DMD gene, is a Schwann cell-specific isoform encoded by a transcript corresponding to DMD exons 56–79, starting from a promoter/exon S1 within intron 55. The physiological roles of Dp116 are poorly understood, because of its extensive homology with other isoforms and its expression in specific tissues. This review summarizes studies on Dp116, focusing on clinical findings and alternative activation of the upstream translation initiation codon that is predicted to produce Dp118.
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spelling pubmed-56641012017-11-06 Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene Matsuo, Masafumi Awano, Hiroyuki Matsumoto, Masaaki Nagai, Masashi Kawaguchi, Tatsuya Zhang, Zhujun Nishio, Hisahide Genes (Basel) Review The Duchenne muscular dystrophy (DMD) gene is one of the largest genes in the human genome. The gene exhibits a complex arrangement of seven alternative promoters, which drive the expression of three full length and four shorter isoforms. Dp116, the second smallest product of the DMD gene, is a Schwann cell-specific isoform encoded by a transcript corresponding to DMD exons 56–79, starting from a promoter/exon S1 within intron 55. The physiological roles of Dp116 are poorly understood, because of its extensive homology with other isoforms and its expression in specific tissues. This review summarizes studies on Dp116, focusing on clinical findings and alternative activation of the upstream translation initiation codon that is predicted to produce Dp118. MDPI 2017-10-02 /pmc/articles/PMC5664101/ /pubmed/28974057 http://dx.doi.org/10.3390/genes8100251 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Matsuo, Masafumi
Awano, Hiroyuki
Matsumoto, Masaaki
Nagai, Masashi
Kawaguchi, Tatsuya
Zhang, Zhujun
Nishio, Hisahide
Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title_full Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title_fullStr Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title_full_unstemmed Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title_short Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene
title_sort dystrophin dp116: a yet to be investigated product of the duchenne muscular dystrophy gene
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664101/
https://www.ncbi.nlm.nih.gov/pubmed/28974057
http://dx.doi.org/10.3390/genes8100251
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