Huebner K, Cannizzaro L A, Nakamura T, Hillova J, Mariage-Samson R, Hecht F, Hill M, Croce C M
Wistar Institute of Anatomy and Biology, Philadelphia, Pennsylvania 19114.
Oncogene. 1988 Oct;3(4):449-55.
The transfection recombinant transforming gene, tre, originated from discontinuous human genetic elements after transfection of NIH3T3 cells with genomic DNA from a Ewing's sarcoma cell line. Probes for the three normally discontinuous human elements involved in the transfection recombinant were subcloned and used in conjunction with a panel of rodent-human hybrid cells to determine their normal location in the human genome. The leftmost (5') element derives from the long arm of chromosome 5 (5q); the internal fragment derives from human chromosome 18 proximal to the bcl-2 gene; and the rightmost (3') element derives from the long arm of chromosome 17 (17q) distal to an acute leukemia breakpoint at 17q21. In situ hybridization of the same probes to human metaphase chromosomes confirmed localization of these sequences to regions 5q23----q31, 18q12, and 17q12----q22.
转染重组转化基因tre,是在用尤因肉瘤细胞系的基因组DNA转染NIH3T3细胞后,源自不连续的人类遗传元件。参与转染重组的三个通常不连续的人类元件的探针被亚克隆,并与一组啮齿动物-人类杂交细胞一起使用,以确定它们在人类基因组中的正常位置。最左边(5')的元件来自5号染色体长臂(5q);内部片段来自靠近bcl-2基因的人类18号染色体;最右边(3')的元件来自17号染色体长臂(17q),位于17q21急性白血病断点的远端。将相同的探针与人中期染色体进行原位杂交,证实这些序列定位于5q23----q31、18q12和17q12----q22区域。