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

T. F. Krulewski, P. E. Neumann, J. W. Gordon

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Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)3709-3712
Número de páginas4
PublicaciónProceedings of the National Academy of Sciences of the United States of America
Volumen86
N.º10
DOI
EstadoPublished - may. 1989
Publicado de forma externa

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