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Cloning and chromosomal mapping of the mouse DNA-dependent protein kinase gene
Authors:Kiyohiro Hamatani  Yoichi Matsuda  Ryoko Araki  Masahiro Itoh  M Abe
Institution:(1) Cell Biology Laboratory, Department of Radiobiology, Radiation Effects Research Foundation, 8-6 Nakagawa 1 chome, Nagasaki 850, Japan, JP;(2) Laboratory of Animal Genetics, Nagoya University School of Agricultural Sciences, Furou-cho, Chigusa-ku, Nagoya 464-01, Japan, JP;(3) Division of Biology and Oncology, National Institute of Radiological Sciences, 4-9-1 Anagawa, Chiba 263, Japan, JP
Abstract: Severe combined immune deficiency (scid) mice are assumed to have two types of abnormalities: one is high radiosensitivity and the other is abnormal recombination in immunoglobulin and T-cell receptor genes. The human chromosome 8 q1.1 region has an ability to complement the scid aberrations. Moreover, the localization of the subunit DNA-dependent protein kinase DNA-PKcs] participating in DNA double-strand break repair in the same locus was clarified. In scid mouse cells, the number of DNA-PKcs products and extent of DNA-PK activity remarkably decrease. These observations gave rise to the assumption that DNA-PKcs is the scid factor itself. In order to determine whether the DNA-PK cs gene is the scid gene, we isolated the mouse DNA-PK cs gene and investigated its chromosomal locus by fluorescence in situ hybridization (FISH). Consequently, it became clear that the mouse DNA-PK cs gene existed in the centromeric region of mouse chromosome 16, determined by cross-genetic study, as a scid locus. This finding strongly suggests that mouse DNA-PK cs is the scid gene. Received: 22 March 1996
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