Chen S J, Chen Z, Font M P, d'Auriol L, Larsen C J, Berger R
Unité INSERM U 301 and SDI CNRS no. 159541, CNRS, Hôpital Saint-Louis, Paris, France.
Nucleic Acids Res. 1989 Oct 11;17(19):7631-42. doi: 10.1093/nar/17.19.7631.
In the Philadelphia positive bcr negative acute leukemias (Ph1+bcr- AL), the chromosomal breakpoints on chromosome 22 have been shown clustered within 10.8kb (bcr2) and 5kb (bcr3) fragments of the first intron of the BCR gene. We previously reported that the breakpoints were localized in Alu repeats on chromosomes 9 and 22 in a Ph1+bcr- acute lymphoblastic leukemia with a rearrangement involving bcr2. Molecular data of two other Ph1 translocations, one a Ph1+bcr- acute myeloblastic leukemia in the bcr2 region, and the other an acute lymphoblastic leukemia in the bcr3 region are presented. In the former, the breakpoints on chromosomes 9 and 22 are localized in Alu repeats, in regions with two inverted Alu sequences, as in our previously reported case. In the second leukemia, the breakpoints are not located in Alu sequences, but such repeats are found in their vicinity. The implications of these findings are discussed.
在费城染色体阳性、bcr阴性的急性白血病(Ph1+bcr-AL)中,22号染色体上的染色体断点已显示聚集在BCR基因第一内含子的10.8kb(bcr2)和5kb(bcr3)片段内。我们先前报道,在一例涉及bcr2重排的Ph1+bcr-急性淋巴细胞白血病中,断点定位于9号和22号染色体上的Alu重复序列中。本文展示了另外两例Ph1易位的分子数据,一例是bcr2区域的Ph1+bcr-急性髓细胞白血病,另一例是bcr3区域的急性淋巴细胞白血病。在前者中,9号和22号染色体上的断点定位于Alu重复序列中,位于有两个反向Alu序列的区域,如同我们先前报道的病例。在第二种白血病中,断点并不位于Alu序列中,但在其附近发现了此类重复序列。本文讨论了这些发现的意义。