Comparative genome mapping of the ataxia-telangiectasia region in mouse, rat, and Syrian hamster

Genomics

Volumn 34, Issue 3, 1996, Pages 347-352

  Matsuda, Yoichi ^a,e   Imai, Takashi ^a   Shiomi, Tadahiro ^a   Saito, Toshiyuki ^a   Yamauchi, Masatake ^a   Fukao, Toshiyuki ^b   Akao, Yukihiro ^c   Seki, Naohiko ^d   Ito, Hiroko ^a   Hori, Tada Aki ^a  

^a NATIONAL INSTITUTE OF RADIOLOGICAL SCIENCES   (Japan)

^b GIFU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c OSAKA MEDICAL COLLEGE   (Japan)

^d KAZUSA DNA RESEARCH INSTITUTE   (Japan)

^e NAGOYA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ANIMAL CELL; ARTICLE; ATAXIA TELANGIECTASIA; CHROMOSOME 11Q; CHROMOSOME 12Q; CHROMOSOME 8; CHROMOSOME 9; CHROMOSOME BREAKAGE; CHROMOSOME INVERSION; CHROMOSOME MAP; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENOME; HUMAN; MOUSE; NONHUMAN; PRIORITY JOURNAL; RAT; SYRIAN HAMSTER;

ANIMALIA; ATAXIA; ATAXIA TELANGIECTASIA; CRICETINAE; MESOCRICETUS AURATUS; RODENTIA;

EID: 0030585751     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0297     Document Type: Article

References (27)

1. Akao, Y., Seto, M., Takahashi, T., Kubonishi, I., Miyoshi, I., Nakazawa, S., Tsujimoto, Y., Croce, C. M., and Ueda, R. (1991). Molecular cloning of the chromosomal breakpoint of a B-cell lymphoma with the t(11;14)(q23;q32) translocation. Cancer Res. 51: 1574-1576.
2. Akao, Y., Seto, M., Yamamoto, K., Iida, S., Nakazawa, S., Inazawa, J., Abe, T., Takahashi, T., and Ueda, R. (1992). The RCK gene associated with t(11;14) translocation is distinct from the MLL/ALL-1 gene with t(4;11) and t(11;19) translocations. Cancer Res. 52: 6083-6087.
3. Ambrose, H. J., Byrd, P. J., McConville, C. M., Cooper, P. R., Stankovic, T., Riley, J. H., Shiloh, Y., McNamara, J. O., Fukao, T., and Taylor, M. R. (1994). A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia. Genomics 21: 612-619.
4. Charmley, P., Nguyen, J., Wei, S., and Gatti, R. A. (1991). Genetic linkage analysis and homology relationships of genes located on human chromosome 11q. Genomics 10: 608-617.
5. Evans, E. P. (1989). Standard idiogram. In "Genetic Variants and Strains of the Laboratory Mouse" (M. F. Lyon and A. G. Searle, Eds.), pp. 576-578, Oxford Univ. Press, Oxford.
6. Fukao, T., Kamijo, K., Osumi, T., Fujiki, Y., Yamaguchi, S., Orii, T., and Hashimoto, T. (1989). Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase. J. Biochem. 106: 197-204.
7. Harada, Y-N., Matsuda, Y., Shiomi, N., and Shiomi, T. (1995). Complementary DNA sequence and chromosomal localization of xpg, the mouse counterpart of human repair gene XPG/ERCC5. Genomics 28: 59-65.
8. Imai, K., and Kingsley, D. M. (1994). Mouse Chromosome 9. Mamm. Genome 5: S139-S153.
9. Imai, T., Seki, N., Saito, T., Yamauchi, M., Matsuda, Y., Ito, H., Ogiwara, A., Nomura, N., and Hori, T. (1995). Construction of YAC contigs at human chromosome 11q22.3-q23.1 region covering the ataxia telangiectasia locus. DNA Res. 2: 113-121.
10. Imai, T., Yamauchi, M., Seki, N., Sugawara, T., Saito, T., Matsuda, Y., Ito, H., Nagase, T., Nomura, N., and Hori, T. (1996). Identification and characterization of a new gene physically linked to the ATM gene. Genome Res., in press.
11. James, M. R., Richard, C. W. III, Schott, J-J., Yousry, C., Clark, K., Bell, J., Terwilliger, J. D., Hazan, J., Dubay, C., Vignal, A., Agrapart, M., Imai, T., Nakamura, Y., Polymeropoulos, M., Weissenbach, J., Cox, D. R., and Lathrop, G. M. (1994). A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nature Genet. 8: 70-76.
12. Li, S., Pathak, S., and Hsu, T. C. (1982). High resolution G-banding patterns of Syrian hamster chromosomes. Cytogenet. Cell Genet. 33: 295-302.
13. Lyon, M. F., and Kirby, M. C. (1995). Mouse chromosome atlas. Mouse Genome 93: 23-66.
14. Masuno, M., Kano, M., Fukao, T., Yamaguchi, S., Osumi, T., Hashimoto, T., Takahashi, E., Hori, T., and Orii, T. (1992). Chromosome mapping of the human mitochondrial acetoacetyl-coenzyme A thiolase gene to 11q22.3-q23.1 by fluorescence in situ hybridization. Cytogenet. Cell Genet. 60: 121-122.
15. Matsuda, Y., Harada, Y.-N., Natsuume-Sakai, S., Lee, K., Shiomi, T., and Chapman, V. M. (1992). Location of the mouse complement factor H gene (cfh) by FISH analysis and replication R-banding. Cytogenet. Cell Genet. 61: 282-285.
16. Matsuda, Y., and Chapman, V. M. (1995). Application of fluorescence in situ hybridization in genome analysis of the mouse. Electrophoresis 16: 261-272.
17. McConville, C. M., Byrd, P. J., Ambrose, H. J., Stankovic, T., Ziv, Y., Bar-Shira, A., Vanagaite, L., Rotman, G., Shiloh, Y., Gillett, G. T., Riley, J. H., and Taylor, A. M. R. (1993). Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangietasia locus on chromosome 11q22-q23. Hum. Mol. Genet. 2: 969-974.
18. McNamara, J. O., Eubanks, J. H., McPherson, J. D., Wasmuth, J. J., Evans, G. A., and Heinemann, S. F. (1992). Chromosomal localization of human glutamate receptor genes. J. Neurosci. 12: 2555-2562.
19. Mullins, L. J., Stephenson, D. A., Grant, S. G., and Chapman, V. M. (1990). Efficient linkage of 10 loci in the proximal region of the mouse X chromosome. Genomics 7: 19-30.
20. Saito, T., Matsuda, Y., Ito, H., Fusaki, N., Hori, T., and Yamamoto, T. (1996). Localization of ZAP-70, the gene for a T cell-specific protein tyrosine kinase, to mouse and rat chromosomes by fluorescence in situ hybridization and molecular linkage analyses. Mamm. Genome, in press.
21. Satoh, H., Yoshida, M. C., and Sasaki, M. (1989). High resolution chromosome banding in the Norway rat, Rattus norvegicus. Cytogenet. Cell Genet. 50: 151-154.
22. Savitsky, K., Bar-Shira, A., Gilad, S., Rotman, G., Ziv, Y., Vanagaite, L., Tagle, D. A., Smith, S., Uziel, T., Sfez, S., Ashkenazi, M., Pecker, I., Frydman, M., Harnik, R., Patanjali, S. R., Simmons, A., Clines, G. A., Sartiel, A., Gatti, R. A., Chessa, L., Sanal, O., Lavin, M. F., Jaspers, N. G. J., Taylor, A. M. R., Arlett, C. F., Miki, T., Weissman, S. M., Lovett, M., Collins, F. S., and Shiloh, Y. (1995a). A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268: 1749-1753.
23. Savitsky, K., Sfez, S., Tagle, D. A., Ziv, Y., Sartiel, A., Collins, F. S., Shiloh, Y., and Rotman, G. (1995b). The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species. Hum. Mol. Genet. 4: 2025-2032.
24. Sedgwick, R. P., and Boder, E. (1991). Ataxia telangiectasia. In "Hereditary Neuropathies and Spinocerebellar Atrophies" (J. M. B. V. de Jong, Ed.), pp. 347-423, Elsevier, Amsterdam.
25. Somssich, I. E., and Hameister, H. (1989). Standard karyotype of early replicating bands (RBG-banding). In "Genetic Variants and Strains of the Laboratory Mouse" (M. F. Lyon and A. G. Searle, Eds.), pp. 580-581, Oxford Univ. Press, Oxford.
26. Taylor, A. M. R., Byrd, P. J., McConville, C. M., and Thacker, S. (1994). Genetic and cellular features of ataxia telangiectasia. Int. J. Radiat. Biol. 65: 65-70.
27. Yamada, J., Kuramoto, T., and Serikawa, T. (1994). A rat genetic linkage map and comparative maps for mouse or human homologous rat genes. Mamm. Genome 5: 63-83.