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PMID: 2726749 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Insertional mutation in a transgenic mouse allelic with Purkinje cell degeneration.

Krulewski TF, Neumann PE, Gordon JW

Abstract

Purkinje cell degeneration (pcd) is an autosomal recessive mutation which maps to chromosome 13 in the mouse. The pcd mutation causes loss of cerebellar Purkinje cells, retinal photoreceptor cells, and olfactory bulb mitral cells, as well as abnormalities of spermatogenesis. pcd is among a number of autosomal recessive mutations in mice and humans that affect neurologic function and male fertility. The cloning of one or more of these loci would contribute significantly to our understanding of the genetic control of development and maintenance of affected cell types. We report here identification of a transgenic mouse line with an insertional mutation that is allelic with pcd and manifests histopathologic features indistinguishable from those of the spontaneous mutation. The creation of an allele of pcd by transgene insertion should make possible the cloning of the pcd locus.

MeSH Terms
Alleles Animals Blotting, Southern Cloning, Molecular Infertility, Male/genetics Male Mice Mice, Transgenic Mutation Nerve Degeneration Phenotype Purkinje Cells/pathology Spermatogenesis
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Krulewski T F
Department of Human Genetics, Brookdale Center for Molecular Biology, Mount Sinai School of Medicine, New York, NY 10029.
Neumann P E
Gordon J W
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1989-05-00
Pages
3709-12
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC287209
Subset
IM
Grants
NCI NIH HHS · CA42103 · United States
NICHD NIH HHS · HD20484 · United States
NINDS NIH HHS · NS20820 · United States
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