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在伴有隐匿性费城染色体的慢性髓性白血病中,BCR/ABL融合基因位于9号染色体上。

BCR/ABL fusion located on chromosome 9 in chronic myeloid leukemia with a masked Ph chromosome.

作者信息

Mohamed A N, Koppitch F, Varterasian M, Karanes C, Yao K L, Sarkar F H

机构信息

Department of Pathology, Harper Hospital, Wayne State University, Detroit, Michigan 48201, USA.

出版信息

Genes Chromosomes Cancer. 1995 Jun;13(2):133-7. doi: 10.1002/gcc.2870130210.

Abstract

A reciprocal translocation, t(10;22)(q22;q11), resulting in a masked Ph chromosome was identified in a patient diagnosed with chronic myeloid leukemia (CML). Both homologs of chromosome 9 were of the normal pattern. Two signals for the ABL probe, both of them hybridized to chromosome 9, were demonstrated via fluorescence in situ hybridization (FISH). Furthermore, cohybridization with two differently labeled BCR/ABL translocation DNA probes indicated a BCR/ABL fusion apparently located on 9q34. Molecular studies revealed a rearrangement of the BCR region and expression of a chimeric BCR/ABL mRNA of CML configuration. These findings indicate that the BCR/ABL fusion resulted from an unusual relocation of the BCR gene from its normal position on 22q11 to 9q34 adjacent to the ABL gene.

摘要

在一名被诊断为慢性髓性白血病(CML)的患者中,发现了一种相互易位,即t(10;22)(q22;q11),导致出现一条隐匿的费城染色体。9号染色体的两条同源染色体均为正常模式。通过荧光原位杂交(FISH)显示,ABL探针的两个信号均与9号染色体杂交。此外,用两种不同标记的BCR/ABL易位DNA探针进行共杂交表明,BCR/ABL融合明显位于9q34。分子研究揭示了BCR区域的重排以及CML构型的嵌合BCR/ABL mRNA的表达。这些发现表明,BCR/ABL融合是由于BCR基因从其在22q11的正常位置异常重定位到与ABL基因相邻的9q34所致。

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