Genetic and physical maps of the stargazer locus on mouse chromosome 15

Genomics

Volumn 43, Issue 1, 1997, Pages 62-68

  Letts, Verity A ^a   Valenzuela, Alicia ^a   Kirley, Jessica P ^a   Sweet, Hope O ^a   Davisson, Muriel T ^a   Frankel, Wayne N ^a  

^a JACKSON LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG; RECOMBINANT DNA;

ABSENCE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; ATAXIA; CHROMOSOME 15; GENE LOCUS; GENE MAPPING; MOUSE; NONHUMAN; PRIORITY JOURNAL; VESTIBULAR DISORDER; YEAST ARTIFICIAL CHROMOSOME;

ANIMALIA; ATAXIA;

EID: 0031194448     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4780     Document Type: Article

References (44)

1. Adolph, S., Berchtold, M. W., and Hameister, H. (1989). Fine localization of genes on distal murine chromosome 15. Cytogenet. Cell Genet. 52: 177-179.
2. Avraham, K. B., Hasson, T., Steel, K. P., Kingsley, D. M., Russell, L. B., Mooseker, M. S., Copeland, N. G., and Jenkins, N. A. (1995). The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nature Genet. 11: 369-375.
3. Baimbridge, K. G., Celio, M. R., and Rogers, J. H. (1992). Calcium-binding proteins in the nervous system. Trends Neurosci. 15: 303-308.
4. Bar, I., Lambert De Rouvroit, C., Royaux, I., Krizman, D. B., Dernoncourt, C., Ruelle, D., Beckers, M. C., and Goffinet, A. M. (1995). A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments. Genomics 26: 543-549.
5. Berchtold, M. W., Epstein, P., Beaudet, A. L., Payne, M. E., Heizmann, C. W., and Means, A. R. (1987). Structural organization and chromosomal assignment of the parvalbumin gene. J. Biol. Chem. 262: 8696-8701.
6. Bottorff, D., and Stone, J. C. (1992). The murine leukemia inhibition factor gene (Lif) is located on proximal chromosome 11, not chromosome 13. Mamm. Genome 3: 681-684.
7. Brannan, C. I., Gilbert, D. J., Ceci, J. D., Matsuda, Y., Chapman, V. M., Mercer, J. A., Eisen, H., Johnston, L. A., Copeland, N. G., and Jenkins, N. A. (1992). An interspecific linkage map of mouse chromosome 15 positioned with respect to the centromere. Genomics 13: 1075-1081.
8. Budarf, M. L., Perier, F., Barnoski, B. L., Bell, C. J., and Vandenberg, C. A. (1995). Assignment of the human hippocampal inward rectifier potassium channel (HIR) gene to 22q13.1. Genomics 26: 625-629.
9. Casalotti, S. O., Pelaia, G., Yakovlev, A. G., Csikos, T., Grayson, D. R., and Krueger, K. E. (1992). Structure of the rat gene encoding the mitochondrial benzodiazepine receptor. Gene 121: 377-382.
10. Chartier, F. L., Keer, J. T., Sutcliffe, M. J., Henriques, D. A., Mileham, P., and Brown, S. D. M. (1992). Construction of a mouse yeast artificial chromosome library in a recombinant-deficient strain of yeast. Nature Genet. 1: 132-136.
11. D'Arcangelo, G., Miao, G. G., Chen, S. C., Soares, H. D., Morgan, J. I., and Curran, T. (1995). A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374: 719-723.
12. DeLorenzo, R. J. (1991). The challenging genetics of epilepsy. In "Genetic Strategies in Epilepsy Research: Epilepsy Research Supplement" (V. E. Anderson, W. A. Hauser, I. E. Leppik, J. L. Noebels, and S. S. Rich, Eds.), Vol. 4, pp. 3-17, Elsevier, New York.
13. Dietrich, W., Katz, H., Lincoln, S., Shin, H.-S., Friedman, J., Dracopoli, N. C., and Lander, E. S. (1992). A genetic map of the mouse suitable for typing intraspecific crosses. Genetics 131: 423-447.
14. Dietrich, W. F., Miller, J. C., Steen, R. G., Merchant, M., Damron, D., Nahf, R., Gross, A., Joyce, D. C., Wessel, M., Dredge, R. D., Marquis, A., Stein, L. D., Goodman, N., Page, D. C., and Lander, E. S. (1994). A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nature Genet. 7: 220-245.
15. Ebersole, T. A., Chen, Q., Justice, M. J., and Artzt, K. (1996). The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins. Nature Genet. 12: 260-265.
16. Eicher, E. M., and Womack, J. E. (1977). Chromosomal location of soluble glutamic-pyruvic transaminase-1 (Gpt-1) in the mouse. Biochem. Genet. 15: 1-8.
17. Elango, R., Riba, L., Housman, D., and Hunter, K. (1996). Generation and mapping of Mus spretus strain-specific markers for rapid genomic scanning. Mamm. Genome 7: 340-343.
18. Fletcher, C. F., Lutz, C. M., O'Sullivan, T. N., Shaughnessy, J. D., Hawkes, R., Frankel, W. N., Copeland, N. G., and Jenkins, N. A. (1996). Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell 87: 607-617.
19. Francis, F., Zehetner, G., Hoglund, M., and Lehrach, H. (1994). Construction and preliminary analysis of the ICRF human P1 library. Genet. Anal. Tech. Appl. 11: 148-157.
20. Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K. A., Antonio, M., Beisel, K. W., Steel, K. P., and Brown, S. D. (1995). A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374: 62-64.
21. Haldi, M., Perrot, V., Saumier, M., Desai, T., Cohen, D., Cherif, D., Ward, D., and Lander, E. S. (1994). Large human YACs constructed in a rad52 strain show a reduced rate of chimerism. Genomics 24: 478-484.
22. Hamilton, B. A., Frankel, W. N., Kerrebrock, A. W., Hawkins, T. L., FitzHugh, W., Kusumi, K., Russell, L. B., Mueller, K. L., van Berkel, V., Birren, B. W., Kruglyak, L., and Lander, E. S. (1996). Disruption of the nuclear hormone receptor RORalpha in staggerer mice. Nature 379: 736-739.
23. Hirotsune, S., Takahara, T., Sasaki, N., Hirose, K., Yoshiki, A., Ohashi, T., Kusakabe, M., Murakami, Y., Muramatsu, M., Watanabe, S., et al. (1995). The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Nature Genet. 10: 77-83.
24. Huppi, K., Siwarski, D., Eppig, J. T., and Mock, B. A. (1996). Encyclopedia of the mouse genome. V. Mouse chromosome 15. Mamm. Genome 6: S256-70.
25. Kusumi, K., Smith, J. S., Koos, D. S., and Lander, S. (1993). Construction of a large insert yeast artificial chromosome (YAC) library of a mouse genome. Mamm. Genome 4: 321-322.
26. Larin, Z., Monaco, D. B., and Lehrach, H. (1991). Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc. Natl. Acad. Sci. USA 88: 4123-4127.
27. Lyford, G. L., Yamagata, K., Kaufmann, W. E., Barnes, C. A., Sanders, L. K., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Lanahan, A. A., and Worley, P. F. (1995). Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites. Neuron 14: 433-445.
28. Mercer, J. A., Seperack, P. K., Strobel, M. C., Copeland, N. G., and Jenkins, N. A. (1991). Novel myosin heavy chain encoded by murine dilute coat colour locus. Nature 349: 709-713.
29. Noebels, J. L., Qiao, X., Bronson, R. T., Spencer, C., and Davisson, M. T. (1990). Stargazer: A new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures. Epilepsy Res. 7: 129-135.
30. Patil, N., Cox, D. R., Bhat, D., Faham, M., Myers, R. M., and Peterson, A. S. (1995). A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nature Genet. 11: 126-129.
31. Pierce, J. C., Sternberg, N., and Sauer, B. (1992). A mouse genomic library in the bacteriophage P1 cloning system: Organization and characterization. Mamm. Genome 3: 550-558.
32. Qiao, X., Hefti, F., Knusel, B., and Noebels, J. L. (1996). Selective failure of brain-derived neurotrophic factor mRNA expression in the cerebellum of stargazer, a mutant mouse with ataxia. J. Neurosci. 16: 640-648.
33. Qiao, X., and Noebels, J. L. (1993). Developmental analysis of hippocampal mossy fiber outgrowth in a mutant mouse with inherited spike-wave seizures. J. Neurosci. 13: 4622-4635.
34. Rocha, J., Amorim, A., Almeida, V. M., Oliveira, J. P., Leao, M., Tavares, M. C., Pereira, M. S., and Vidal-Pinheiro, L. (1988). Gene dosage evidence for the regional assignment of GPT (glutamate-pyruvate transaminase; E.C. 2.6.1.2) locus to 8q24.2-8qter. Hum. Genet. 80: 299-300.
35. Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989). "Molecular Cloning: A Laboratory Manual," 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
36. Segre, J. A., Nemhauser, J. L., Taylor, B. A., Nadeau, J. H., and Lander, E. S. (1995). Positional cloning of the nude locus: Genetic, physical, and transcription maps of the region and mutations in the mouse and rat. Genomics 28: 549-559.
37. Shizuya, H., Birren, B., Kim, U. J., Mancino, V., Slepak, T., Tachiiri, Y., and Simon, M. (1992). Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector. Proc. Natl. Acad. Sci. USA 89: 8794-8797.
38. Stoye, J. P., Frankel, W. N., and Coffin, J. M. (1991). DNA hybridization in dried gels with fragmented probes: An improvement over blotting techniques. Technique 3: 123-128.
39. Sutherland, G. R., Baker, E., Hyland, V. J., Callen, D. F., Stahl, J., and Gough, N. M. (1989). The gene for human leukemia inhibitory factor (LIF) maps to 22q12. Leukemia 3: 9-13.
40. Taylor, B. A., Rowe, L., and Grieco, D. A. (1993). The MEV mouse linkage testing stock: Mapping 30 novel proviral insertions and establishment of an improved stock. Genomics 16: 380-394.
41. Treco, D. A. (1991). "Preparation of Yeast DNA," Wiley, New York.
42. Yamada, Y., Reisine, T., Law, S. F., Ihara, Y., Kubota, A., Kagimoto, S., Seino, M., Seino, Y., Bell, G. I., and Seino, S. (1992). Somatostatin receptors, an expanding family: Cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase. Mol. Endocrinol. 6: 2136-2142.
43. Yasuda, K., Rens-Domiano, S., Breder, C. D., Law, S. F., Saper, C. B., Reisine, T., and Bell, G. I. (1992). Cloning a novel somatostatin receptor, SSTR3, coupled to adenylylcyclase. J. Biol. Chem. 267: 20422-20428.
44. Zara, F., Bianchi, A., Avanzini, G., Di Donato, S., Castellotti, B., Patel, P. I., and Pandolfo, M. (1995). Mapping of genes predisposing to idiopathic generalized epilepsy. Hum. Mol. Genet. 4: 1201-1207.