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Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart

Plakoglobin (gamma-catenin), a member of the armadillo family of proteins, is a constituent of the cytoplasmic plaque of desmosomes as well as of other adhering cell junctions, and is involved in anchorage of cytoskeletal filaments to specific cadherins. We have generated a null mutation of the plak...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121015/
https://www.ncbi.nlm.nih.gov/pubmed/8858175
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description Plakoglobin (gamma-catenin), a member of the armadillo family of proteins, is a constituent of the cytoplasmic plaque of desmosomes as well as of other adhering cell junctions, and is involved in anchorage of cytoskeletal filaments to specific cadherins. We have generated a null mutation of the plakoglobin gene in mice. Homozygous -/- mutant animals die between days 12-16 of embryogenesis due to defects in heart function. Often, heart ventricles burst and blood floods the pericard. This tissue instability correlates with the absence of desmosomes in heart, but not in epithelia organs. Instead, extended adherens junctions are formed in the heart, which contain desmosomal proteins, i.e., desmoplakin. Thus, plakoglobin is an essential component of myocardiac desmosomes and seems to play a crucial role in the sorting out of desmosomal and adherens junction components, and consequently in the architecture of intercalated discs and the stabilization of heart tissue.
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spelling pubmed-21210152008-05-01 Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart J Cell Biol Articles Plakoglobin (gamma-catenin), a member of the armadillo family of proteins, is a constituent of the cytoplasmic plaque of desmosomes as well as of other adhering cell junctions, and is involved in anchorage of cytoskeletal filaments to specific cadherins. We have generated a null mutation of the plakoglobin gene in mice. Homozygous -/- mutant animals die between days 12-16 of embryogenesis due to defects in heart function. Often, heart ventricles burst and blood floods the pericard. This tissue instability correlates with the absence of desmosomes in heart, but not in epithelia organs. Instead, extended adherens junctions are formed in the heart, which contain desmosomal proteins, i.e., desmoplakin. Thus, plakoglobin is an essential component of myocardiac desmosomes and seems to play a crucial role in the sorting out of desmosomal and adherens junction components, and consequently in the architecture of intercalated discs and the stabilization of heart tissue. The Rockefeller University Press 1996-10-01 /pmc/articles/PMC2121015/ /pubmed/8858175 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title_full Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title_fullStr Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title_full_unstemmed Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title_short Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
title_sort targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121015/
https://www.ncbi.nlm.nih.gov/pubmed/8858175