Iida S, Seto M, Yamamoto K, Komatsu H, Akao Y, Nakazawa S, Ariyoshi Y, Takahashi T, Ueda R
Laboratory of Chemotherapy, Aichi Cancer Center Research Institute, Nagoya.
Jpn J Cancer Res. 1993 May;84(5):532-7. doi: 10.1111/j.1349-7006.1993.tb00172.x.
We studied the breakpoint regions involved in t(11;19)(q23;p13) translocation associated with infantile leukemias. Southern blot analysis with the partial cDNA clone for the MLL gene at 11q23 which we had isolated previously detected gene rearrangements in all three cell lines and three leukemia samples from the patients with t(11;19) translocation, indicating that these breakpoints were clustered within the 8.5 kb BamHI germline fragment detected by the probe. To study the breakpoint region, a genomic library of one of the cell lines, KOCL-33, was made. We have isolated the der(19) allele containing the breakpoint as well as the germline alleles at 19p13 and 11q23. Using the genomic probes on chromosome 19 near the breakpoint, Southern blot analysis was performed. The breakpoints at 19p13 of the two other cell lines and the three leukemia samples were not located within 36 kilobases of the KOCL-33 breakpoint, although pulsed-field gel electrophoresis showed that the breakpoints of all three cell lines were on the same NruI fragment of 230 kilobases. These results showed that the breakpoints at 19p13 were not clustered like those at 11q23 in t(11;19) translocation.
我们研究了与婴儿白血病相关的t(11;19)(q23;p13)易位所涉及的断点区域。用我们之前分离得到的位于11q23的MLL基因部分cDNA克隆进行Southern印迹分析,在所有三个细胞系以及来自t(11;19)易位患者的三个白血病样本中均检测到基因重排,这表明这些断点聚集在探针检测到的8.5 kb BamHI种系片段内。为了研究断点区域,构建了其中一个细胞系KOCL-33的基因组文库。我们分离出了包含断点的der(19)等位基因以及19p13和11q23处的种系等位基因。使用靠近断点的19号染色体上的基因组探针进行Southern印迹分析。另外两个细胞系以及三个白血病样本在19p13处的断点并不位于KOCL-33断点的36千碱基范围内,尽管脉冲场凝胶电泳显示所有三个细胞系的断点都在230千碱基的同一片段NruI上。这些结果表明,在t(11;19)易位中,19p13处的断点不像11q23处的断点那样聚集。