Isolation and mapping of novel mouse brain cDNA clones containing trinucleotide repeats, and demonstration of novel alleles in recombinant inbred strains

Genome Research

Volumn 6, Issue 8, 1996, Pages 715-723

  Chambers, Doreen M ^a   Abbott, Catherine M ^a  

^a WESTERN GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; TRINUCLEOTIDE;

ALLELE; ARTICLE; CHROMOSOME FRAGILE SITE; CONTROLLED STUDY; DISEASE SEVERITY; GENE ISOLATION; GENE MAPPING; GENE MUTATION; GENETIC DISORDER; GENETIC LINKAGE; INBREEDING; MOUSE; NEWBORN; NONHUMAN; PATHOGENESIS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

ANIMALIA; MUS; MUS MUSCULUS MUSCULUS; MUS SPRETUS; MUSCULUS;

EID: 0029782977     PISSN: 10549803     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.6.8.715     Document Type: Article

References (20)

1. Abbott, C. and D. Chambers. 1994. Analysis of CAG trinucleotide repeats from mouse cDNA sequences. Annu. Hum. Genet. 58: 87-94.
2. Ashley, C.T. and S.T. Warren. 1995. Trinucleotide repeat expansion and human disease. Annu. Rev. Genet. 29: 703-728.
3. Bakker, C.E., C. Verheij, R. Willemsen, R. Vanderheim, F. Oerlemans, M. Vermey, A. Bygrave, A.T. Hoogeveen, B.A. Oostra, E. Reyniers, K. Deboulle, R. Dhooge, P. Cras, D. Vanvelzen, G. Nagels, J.J. Martin, P.P. Dedeyn, J.K. Darby, and P.J. Willems. 1994. FMR1 knockout mice - a model to study fragile X mental retardation. Cell 78: 23-33.
4. Beckman, J.S. and J.L. Weber. 1992. Survey of human and rat microsatellites. Genomics 12: 627-631.
5. Bingham, P.M., M.O. Scott, S.P. Wang, M.J. Mcphaul, E.M. Wilson, J.Y. Garbern, D.E. Merry, and K.H. Fischbeck. 1995. Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice. Nature Genet. 9: 191-196.
6. Braga, E.A., B.I. Kapanadze, N.S. Kupriyanova, G.M. Ivanova, V.M. Brodyanskii, K.K. Nechvolodov, G.A. Skutov, A.P. Ryskov, V.V. Nosikov, and N.K. Yankovskii. 1995. Distribution analysis of 7 microsatellite motifs in cosmids of human chromosome 13 library. Mol. Biol. 29: 584-590.
7. Burright, E.N., H.B. Clark, A. Servadio, T. Matilla, R.M. Feddersen, W.S. Yunis, L.A. Duvick, H.Y. Zoghbi, and H.T. Orr. 1995. SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat. Cell 82: 937-948.
8. Campuzano, V., L. Montermini, M.D. Molto, L. Pianese, M. Cossee, F. Cavalcanti, E. Monros, F. Rodius, F. Duclos, A. Monticelli, F. Zara, J. Canizares, H. Koutnikova, S. Bidichandani, C. Gellera, A. Brice, P. Trouillas, G. De Michele, A. Filla, R. De Frutos, F. Palau, P.I. Patel, S. Di Donato, J.-L. Mandel, S. Cocozza, M. Koenig, and M. Pandolfo. 1996. Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271: 1423-1427.
9. Dietrich, W., H. Katz, S.E. Lincoln, H.-S. Shin, J. Friedman, N.C Dracopoli, and E.S. Lander. 1993. A genetic map of the mouse suitable for typing intraspecific backcrosses. Genetics 131: 423-447.
10. Li, S-H., M.G. McInnis, R.L. Margolis, S.E. Antonarakis, and C.A. Ross. 1993. Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms. Genomics 16: 572-579.
11. Manly, K.F. 1993. A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm. Genome 4: 303-313.
12. Myers, R.H., M.E. MacDonald, W.J. Koroshetz, M.P. Duyao, C.M. Ambrose, S.A.M. Taylor, G. Barnes, J. Srinidhi, C.S. Lin, W.L. Whaley, A.M. Lazzarini, M. Schwartz, G. Wolff, E.D. Bird, J.-P.G. Vonsattel, and J.F. Gusella. 1993. De novo expansion of a (CAG)n repeat in Huntington's disease. Nature Genet. 5: 168-173.
13. Ricke, D.O., Q. Liu, B. Gostout, and S.S. Sommer. 1995. Nonrandom patterns of simple and cryptic triplet repeats in coding and noncoding sequences. Genomics 26: 510-520.
14. Riggins, R.G., L.K. Lokey, J.L. Chastain, H.A. Leiner, S.L. Sherman, K.D. Wilkinson, and S.T. Warren. 1992. Human genes containing polymorphic trinucleotide repeats. Nature Genet. 2: 186-191.
15. Rinchik, E.M. and L.B. Russell. 1990. Germ-line deletion mutations in the mouse: Tools for intensive functional and physical mapping of regions of the mammalian genome. In Genetic and physical mapping (ed. K.E. Davies and S.M. Tilghman), pp. 121-158. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
16. Rowe, L.B., J.H. Nadeau, R. Turner, W.N. Frankel, V.A. Letts, J.T. Eppig, M.S.H. Ko, S.J. Thurston, and E.H. Birkenmeier. 1994. Maps from two interspecific backcross DNA panels available as a community genetic mapping resource. Mamm. Genome 5: 253-274.
17. Stallings, R.L. 1994. Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequence-implications for human genetic diseases. Genomics 21: 116-121.
18. van der Spek, P.J., C.E. Visser, F.H. Hanaoka, B. Smit, A. Hagemeijer, D. Bootsma, and J.H.J. Hoeijmakers. 1996. Cloning, comparative mapping, and RNA expression of the mouse homologues of the Saccharomyces cerevisiae nucleotide excision repair gene RAD23. Genomics 31: 20-27.
19. 2+-ATPases isoforms 2 (ATPB2) and 3 (ATPB3) to human chromosomes 3p26-p25 and Xq28, respectively. Cyogenet. Cell Genet. 67: 41-45.
20. Weber, J.L. 1990. Informativeness of human (dC-dA)n (dG-dT)n polymorphisms. Genomics 7: 524-530.