Novel exonic mutation (5319 G to A) resulting in two aberrantly spliced transcripts of the ATM gene in a Japanese patient with ataxia-telangiectasia
Corresponding Author
Toshiyuki Fukao
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Dept. of Pediatrics, Gifu University School of Medicine, Gifu 500, JapanSearch for more papers by this authorHideaki Tashita
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorTakahide Teramoto
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorRyosuke Inoue
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorHideo Kaneko
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorKayo Komiyama
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorAnat Bar-Shira
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorShlomit Gilad
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorYosef Shiloh
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorMasaaki Nishimura
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorNaomi Kondo
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorCorresponding Author
Toshiyuki Fukao
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Dept. of Pediatrics, Gifu University School of Medicine, Gifu 500, JapanSearch for more papers by this authorHideaki Tashita
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorTakahide Teramoto
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorRyosuke Inoue
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorHideo Kaneko
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorKayo Komiyama
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorAnat Bar-Shira
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorShlomit Gilad
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorYosef Shiloh
Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorMasaaki Nishimura
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this authorNaomi Kondo
Department of Pediatrics, Gifu University School of Medicine, Gifu, Japan
Search for more papers by this author
References
- Ambrose HJ, Byrd PJ, McConville CM, Cooper PR, Stankovic T, Riley JH, Shiloh Y, McNamara JO, Fukao T, Taylor AMR (1994) A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia. Genomics 21: 612–619.
- Bassam BJ, Caetano-Anolles G, Gresshoff PM (1991) Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 196: 80–83.
- Gatti RA, Berkel I, Boder E, Charmley R, Concannon P, Ersoy R, Foroud T, Jaspers NG, Lange K, Lathrop GM, Leppert M, Nakamura Y, O'connell P, Paterson M, Salser W, Sonal O, Silver J, Sparkes RS, Susi E, Weeks DE, Wei S, White R, Yoder F (1988) Localization of an ataxia-telangiectasia gene to chromosome IIq22–23. Nature 336: 577–580.
- Gilad S, Khosravi R, Shkedy D, Uziel T, Ziv Y, Savitsky K, Rotman G, Smith S, Chessa L, Jorgensen TJ, Harnik R, Frydman M, Sanal O, Portnoi S, Goldwicz Z, Jaspers NGJ, Gatti RA, Lenoir G, Lavin MF, Tatsumi K, Wegner RD, Shiloh Y, Bar-Shira A (1996) Predominance of null mutations in ataxia-telangiectasia. Hum Mol Genet 5: 433–439.
- Harnden DG (1994) The nature of ataxia-telangiectasia: Problems and perspectives. Int J Radiat Biol 66: S13–S19.
- Kondo N, Inoue R, Nishimura S, Kasahara K, Kameyama T, Miwa Y, Lorenzo PR, Orii T (1993) Defective calcium-dependent signal transduction in T lymphocytes of ataxia-telangiectasia. Scand J Immunol 38: 45–48.
- Qiang L, Sommer SS (1995) Restriction endonuclease fingerprinting (REF): A sensitive method for screening mutations in long, contiguous segments of DNA. BioTechniques 18: 470–477.
- Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, Ashkenazi M, Pecker I, Frydman M, Harnik R, Patanjali SR, Simmons A, Clines GA, Sartiel A, Gatti RG, Chessa L, Sanal O, Lavin MF, Jaspers NGJ, Taylor AMR, Arlett CF, Miki T, Weissman SM, Lovett M, Collins FS, Shiloh Y (1995a) A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268: 1749–1753.
- Savitsky K, Sfez S, Tagle DA, Ziv Y, Sartiel A, Collins FS, Shiloh Y, 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.
- Shapiro MB, Senapathy P (1987) RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucleic Acids Res 15: 7155–7175.
- Telatar M, Wang Z, Udar N, Liang T, Bernatowska-Matuszkiewicz E, Lavin M, Shiloh Y, Concannon P, Good RA, Gatti RA (1996) Ataxia-telangiectasia: Mutations in ATM cDNA detected by protein-truncation screening. Am J Hum Genet 59: 40–44.
- Uziel T, Savitsky K, Platzer M, Ziv Y, Helbitz T, Nehls M, Boehm T, Rosenthal A, Shiloh Y, Rotman G (1996) Genomic organization of the ATM gene. Genomics 33: 317–320.