A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse

Genomics

Volumn 42, Issue 3, 1997, Pages 393-396

  Roderick, Thomas H ^a   Chang, Bo ^a   Hawes, Norman L ^a   Heckenlively, John R ^b  

^a JACKSON LABORATORY   (United States)

^b JULES STEIN EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; ARTICLE; CENTROMERE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1P; CHROMOSOME 4; CHROMOSOME 8Q; CHROMOSOME BREAKAGE; CHROMOSOME INVERSION; ELECTRORETINOGRAPHY; GENE MAPPING; MALE; MOUSE; NONHUMAN; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; RETINA BLOOD VESSEL; RETINA DEGENERATION; RETINA PIGMENT DEGENERATION; TELOMERE;

ANIMALIA;

EID: 0031570686     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4717     Document Type: Article

References (20)

1. Blanton, S. H., Heckenlively, J. R., Cottingham, A. W., Friedman, J., Sadler, L. A., Wagner, M., Friedman, L. H., and Daiger, S. P. (1991). Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics 11: 857-869.
2. Chang, B., Heckenlively, J. R., Hawes, N. L., and Roderick, T. H. (1993). New mouse primary retinal degeneration (rd-3). Genomics 16: 45-49.
3. Chang, B., Bronson, R. T., Hawes, N. L., Roderick, T. H., Peng, C., Hageman, G. S., and Heckenlively, J. R. (1994). Retinal degeneration in motor neuron degeneration: A mouse model of ceroid lipo-fuscinosis. Invest. Ophthalmol. Vis. Sci. 35: 1071-1076.
4. Davisson, M. T., and Akeson, E. C. (1987). An improved method for preparing G-banded chromosomes from mouse peripheral blood. Cytogenet. Cell Genet. 45: 70-74.
5. Finlayson, J. S., Potter, M., and Runner, C. C. (1963). Eletrophoretic variation and sex dimorphism of the major urinary protein complex of inbred mice: A new genetic marker. J. Natl. Cancer Inst. 31: 91-107.
6. Flannery, J., Lem, J., Simon, M., Applebury, M., Li, T., Bowes, C., and Farber, D. (1992). Transgenic rescue of the rd/rd phenotype. Invest. Ophthalmol. Vis. Sci. 33: 945. [ARVO Abstracts]
7. Heckenlively, J. R., Winston, J. V., and Roderick, T. H. (1989). Screening for mouse retinal degeneration. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology. Doc. Ophthalmol. 71: 229-239.
8. Heckenlively, J. R., Chang, B., Peng, C., Erway, L. C., Hawes, N. L., Hageman, G. S., and Roderick, T. H. (1995). A mouse model (rd5) for Usher Syndrome: linkage mapping suggests homology to Usher Type I reported at human chromosome 11p15. Proc. Natl. Acad. Sci. USA 92: 11100-11104.
9. Mouse Genome Database (MGD) (1996). Mouse Genome Informatics Project, The Jackson Laboratory, Bar Harbor, ME (Available, http://www.informatics.jax.org/).
10. Mullen, R. J., Eicher, E. M., and Sidman, R. L. (1976). Purkinje cell degeneration, a new neurological mutation in the mouse. Proc. Natl. Acad. Sci. USA 73: 208-212.
11. Roderick, T. H. (1983). Using inversions to detect and study recessive lethals and detrimentals in mice. In "Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk" (F. J. deSerres and W. Sheridan, Eds.), pp. 135-167, Plenum, New York.
12. Roderick, T. H., and Hawes, N. L. (1970). Two radiation-induced chromosomal inversions in mice (Mus musculus). Proc. Natl. Acad. Sci. USA 67: 961-967.
13. Roderick, T. H., and Hawes, N. L. (1974). Nineteen paracentric chromosomal inversions in mice. Genetics 76: 109-117.
14. Ruddle, F. H., Shows, T. B., and Roderick, T. H. (1968). Autosomal control of an electrophoretic variant of glucose-6-phosphate dehydrogenase in the mouse (Mus musculus). Genetics 58: 599-606.
15. Shows, T. B., Ruddle, F. H., and Roderick, T. H. (1969). Phosphoglucomutase electrophoretic variants in the mouse. Biochem. Genet. 3: 25-35.
16. Sidman, R. L., and Green, M. C. (1965). Retinal degeneration in the mouse: Location of the rd locus in linkage group XVII. J. Hered. 56: 23-29.
17. Sidman, R. L., and Green, M. C. (1970). Nervous, a new mutant mouse with cerebellar disease. In "Les mutants pathologiques chez l'animal" (M. Sabourdy, Ed.), pp. 69-79, Centre National de la Recherche Scientific, Paris.
18. Travis, G. H., Groshan, K. R., Lloyd, M., and Bok, D. (1992). Complete rescue of outer segment dysplasia and photoreceptor degeneration in transgenic retinal degeneration slow (rds) mice. Invest. Ophthalmol. Vis. Sci. 33: 946. [ARVO Abstracts]
19. Van Nie, R., Ivanyi, D., and Demant, P. (1978). A new H-2 linked mutation, rds, causing retinal degeneration in the mouse. Tissue Antigens 12: 106-108.
20. Yokoyama, T., Hanten, G., Baehr, W., and Overbeek, P. A. (1992). Partial rescue of the rd mutation by photoreceptor-specific expression of cGMP phosphodiesterase beta-subunit in transgenic mice. Invest. Ophthalmol. Vis. Sci. 33: 945. [ARVO Abstracts]