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The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle

The Popeye domain containing (POPDC) genes encode transmembrane proteins, which are abundantly expressed in striated muscle cells. Hallmarks of the POPDC proteins are the presence of three transmembrane domains and the Popeye domain, which makes up a large part of the cytoplasmic portion of the prot...

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Detalles Bibliográficos
Autor principal: Brand, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872366/
https://www.ncbi.nlm.nih.gov/pubmed/29534001
http://dx.doi.org/10.3390/jcdd5010018
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author Brand, Thomas
author_facet Brand, Thomas
author_sort Brand, Thomas
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description The Popeye domain containing (POPDC) genes encode transmembrane proteins, which are abundantly expressed in striated muscle cells. Hallmarks of the POPDC proteins are the presence of three transmembrane domains and the Popeye domain, which makes up a large part of the cytoplasmic portion of the protein and functions as a cAMP-binding domain. Interestingly, despite the prediction of structural similarity between the Popeye domain and other cAMP binding domains, at the protein sequence level they strongly differ from each other suggesting an independent evolutionary origin of POPDC proteins. Loss-of-function experiments in zebrafish and mouse established an important role of POPDC proteins for cardiac conduction and heart rate adaptation after stress. Loss-of function mutations in patients have been associated with limb-girdle muscular dystrophy and AV-block. These data suggest an important role of these proteins in the maintenance of structure and function of striated muscle cells.
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spelling pubmed-58723662018-03-30 The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle Brand, Thomas J Cardiovasc Dev Dis Review The Popeye domain containing (POPDC) genes encode transmembrane proteins, which are abundantly expressed in striated muscle cells. Hallmarks of the POPDC proteins are the presence of three transmembrane domains and the Popeye domain, which makes up a large part of the cytoplasmic portion of the protein and functions as a cAMP-binding domain. Interestingly, despite the prediction of structural similarity between the Popeye domain and other cAMP binding domains, at the protein sequence level they strongly differ from each other suggesting an independent evolutionary origin of POPDC proteins. Loss-of-function experiments in zebrafish and mouse established an important role of POPDC proteins for cardiac conduction and heart rate adaptation after stress. Loss-of function mutations in patients have been associated with limb-girdle muscular dystrophy and AV-block. These data suggest an important role of these proteins in the maintenance of structure and function of striated muscle cells. MDPI 2018-03-13 /pmc/articles/PMC5872366/ /pubmed/29534001 http://dx.doi.org/10.3390/jcdd5010018 Text en © 2018 by the author. 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
Brand, Thomas
The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title_full The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title_fullStr The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title_full_unstemmed The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title_short The Popeye Domain Containing Genes and Their Function as cAMP Effector Proteins in Striated Muscle
title_sort popeye domain containing genes and their function as camp effector proteins in striated muscle
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872366/
https://www.ncbi.nlm.nih.gov/pubmed/29534001
http://dx.doi.org/10.3390/jcdd5010018
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