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A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis

The occurrence of a new mutation affecting cartilage and bone in mice is reported. The gene is lethal, shows autosomal recessive inheritance, and has high penetrance. It is not allelic to shorthead and probably not to phocomelia or achondroplasia. It results in a foreshortened face, cleft palate, de...

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Detalles Bibliográficos
Autores principales: Seegmiller, R., Fraser, F. C., Sheldon, H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1971
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108112/
https://www.ncbi.nlm.nih.gov/pubmed/4100752
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author Seegmiller, R.
Fraser, F. C.
Sheldon, H.
author_facet Seegmiller, R.
Fraser, F. C.
Sheldon, H.
author_sort Seegmiller, R.
collection PubMed
description The occurrence of a new mutation affecting cartilage and bone in mice is reported. The gene is lethal, shows autosomal recessive inheritance, and has high penetrance. It is not allelic to shorthead and probably not to phocomelia or achondroplasia. It results in a foreshortened face, cleft palate, defective trachea, and shortened long bones with flared metaphyses. Chondrocytes of epiphyseal cartilage from the mutant are not aligned in columns, and there is a decrease in the usual staining of the cartilage matrix. Electron microscope observations show large, wide collagen fibrils with "native" banding in the matrix of mutant cartilage, which are not present in normal cartilage. Possible explanations for the expression of this genetic disorder of cartilage development are put forward.
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spelling pubmed-21081122008-05-01 A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis Seegmiller, R. Fraser, F. C. Sheldon, H. J Cell Biol Article The occurrence of a new mutation affecting cartilage and bone in mice is reported. The gene is lethal, shows autosomal recessive inheritance, and has high penetrance. It is not allelic to shorthead and probably not to phocomelia or achondroplasia. It results in a foreshortened face, cleft palate, defective trachea, and shortened long bones with flared metaphyses. Chondrocytes of epiphyseal cartilage from the mutant are not aligned in columns, and there is a decrease in the usual staining of the cartilage matrix. Electron microscope observations show large, wide collagen fibrils with "native" banding in the matrix of mutant cartilage, which are not present in normal cartilage. Possible explanations for the expression of this genetic disorder of cartilage development are put forward. The Rockefeller University Press 1971-03-01 /pmc/articles/PMC2108112/ /pubmed/4100752 Text en Copyright © 1971 by The Rockefeller University Press 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 Article
Seegmiller, R.
Fraser, F. C.
Sheldon, H.
A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title_full A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title_fullStr A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title_full_unstemmed A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title_short A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
title_sort new chondrodystrophic mutant in mice : electron microscopy of normal and abnormal chondrogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2108112/
https://www.ncbi.nlm.nih.gov/pubmed/4100752
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