Cherif D, Der-Sarkissian H, Derré J, Tokino T, Nakamura Y, Berger R
Unité INSERM U 301, Paris, France.
Genes Chromosomes Cancer. 1992 Mar;4(2):107-12. doi: 10.1002/gcc.2870040202.
Thirteen cosmid probes were mapped on the long arm of chromosome 11 between 11q22 and 11q24 by nonradioactive in situ hybridization. Starting with these localizations and those of other probes mapped to 11q23, four acute leukemias with translocations involving 11q23 were studied with the same method. The translocation breakpoints of the t(4;11)(q21;q23), t(6;11)(q27;q23), t(9;11)(p21-p22;q23), and t(11;19)(q23;p13) were confirmed to be distal to CD3D. The probe cC111-304 was proximal to the t(11;19) breakpoint while distal to the breakpoints of the other rearrangements. In view of the diversity of chromosomal abnormalities involving band 11q23, our finding extends the molecular heterogeneity of the breakpoint localization in leukemias with rearrangements involving 11q23.
通过非放射性原位杂交技术,将13个黏粒探针定位在11号染色体长臂上11q22和11q24之间的区域。基于这些定位以及其他定位到11q23的探针,采用相同方法对4例伴有涉及11q23易位的急性白血病进行了研究。t(4;11)(q21;q23)、t(6;11)(q27;q23)、t(9;11)(p21-p22;q23)和t(11;19)(q23;p13)的易位断点被证实位于CD3D远端。探针cC111-304位于t(11;19)断点近端,但位于其他重排断点远端。鉴于涉及11q23带的染色体异常具有多样性,我们的发现扩展了伴有涉及11q23重排的白血病断点定位的分子异质性。