A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis
- PMID: 4100752
- PMCID: PMC2108112
- DOI: 10.1083/jcb.48.3.580
A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis
Abstract
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.
Similar articles
-
Studies on cartilage. VI. A genetically determined defect in tracheal cartilage.J Ultrastruct Res. 1972 Feb;38(3):288-301. doi: 10.1016/s0022-5320(72)90006-8. J Ultrastruct Res. 1972. PMID: 4110409 No abstract available.
-
Cartilage matrix deficiency (cmd): a new autosomal recessive lethal mutation in the mouse.J Embryol Exp Morphol. 1978 Feb;43:71-84. J Embryol Exp Morphol. 1978. PMID: 632744
-
Scanning electron microscopy of cartilage in mice with hereditary chondrodysplasia.Scan Electron Microsc. 1982;(Pt 3):1259-67. Scan Electron Microsc. 1982. PMID: 6820573 Review.
-
Parathyroid hormone-related peptide-depleted mice show abnormal epiphyseal cartilage development and altered endochondral bone formation.J Cell Biol. 1994 Sep;126(6):1611-23. doi: 10.1083/jcb.126.6.1611. J Cell Biol. 1994. PMID: 8089190 Free PMC article.
-
The genetics of short stature.Prog Med Genet. 1972;8:243-99. Prog Med Genet. 1972. PMID: 4259833 Review. No abstract available.
Cited by
-
Concordance analysis for QTL detection in dairy cattle: a case study of leg morphology.Genet Sel Evol. 2014 May 19;46(1):31. doi: 10.1186/1297-9686-46-31. Genet Sel Evol. 2014. PMID: 24884971 Free PMC article.
-
Loss of lysyl oxidase-like 3 causes cleft palate and spinal deformity in mice.Hum Mol Genet. 2015 Nov 1;24(21):6174-85. doi: 10.1093/hmg/ddv333. Epub 2015 Aug 24. Hum Mol Genet. 2015. PMID: 26307084 Free PMC article.
-
[Development of vitreous and zonule. VI. The incorporation of 3H-labeled aminoacids and 3H-labeled glucose into the zonule of the mouse during development (author's transl)].Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1973 Dec 18;189(2):105-24. doi: 10.1007/BF00417745. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1973. PMID: 4544040 German. No abstract available.
-
The Transcription Factor HAND1 Is Involved in Cortical Bone Mass through the Regulation of Collagen Expression.Int J Mol Sci. 2020 Nov 16;21(22):8638. doi: 10.3390/ijms21228638. Int J Mol Sci. 2020. PMID: 33207791 Free PMC article.
-
Delay in articular cartilage degeneration of the knee joint by the conditional removal of discoidin domain receptor 2 in a spontaneous mouse model of osteoarthritis.Ann Transl Med. 2020 Sep;8(18):1178. doi: 10.21037/atm-20-5786. Ann Transl Med. 2020. PMID: 33241027 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases