Komatsu K, Ohta T, Jinno Y, Niikawa N, Okumura Y
Department of Radiation Biophysics, Nagasaki University School of Medicine, Japan.
Hum Mol Genet. 1993 Jul;2(7):1031-4. doi: 10.1093/hmg/2.7.1031.
Fragments of human chromosome 8 were introduced into cells derived from murine scid mice via X-irradiation and somatic cell fusion. The resulting hybrid clones contained human DNA fragment(s) which complemented the hyper-radiosensitivity of the scid cells. Alu-PCR products from these hybrids were used for chromosome painting using the technique of chromosome in situ suppression hybridization, allowing assignment of the human HYRC (hyper-radiosensitivity of murine scid mutation, complementing) gene, a candidate for a V(D)J recombinase gene, to human chromosome 8q11.
通过X射线照射和体细胞融合,将人类8号染色体片段导入源自小鼠scid小鼠的细胞中。所得的杂交克隆含有可补充scid细胞超放射敏感性的人类DNA片段。这些杂交体的Alu-PCR产物被用于染色体原位抑制杂交技术进行染色体涂染,从而将人类HYRC(小鼠scid突变超放射敏感性互补)基因(一种V(D)J重组酶基因的候选基因)定位于人类8号染色体q11区域。