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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1 March 1971
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March 01 1971
A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis
R. Seegmiller,
R. Seegmiller
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
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F. C. Fraser,
F. C. Fraser
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
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H. Sheldon
H. Sheldon
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
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R. Seegmiller
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
F. C. Fraser
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
H. Sheldon
From the Departments of Genetics and Pathology, McGill University, Montreal, P. Q., Canada
Received:
June 08 1970
Revision Received:
August 24 1970
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1971 by The Rockefeller University Press
1971
J Cell Biol (1971) 48 (3): 580–593.
Article history
Received:
June 08 1970
Revision Received:
August 24 1970
Citation
R. Seegmiller, F. C. Fraser, H. Sheldon; A NEW CHONDRODYSTROPHIC MUTANT IN MICE : Electron Microscopy of Normal and Abnormal Chondrogenesis . J Cell Biol 1 March 1971; 48 (3): 580–593. doi: https://doi.org/10.1083/jcb.48.3.580
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