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Interstitial insertion of varying amounts of ABL-containing genetic material into chromosome 22 in Ph-negative CML.

作者信息

Rassool F, Martiat P, Taj A, Klisak I, Goldman J

机构信息

MRC/LRF Leukaemia Unit, Hammersmith Hospital, London, U.K.

出版信息

Leukemia. 1990 Apr;4(4):273-7.

PMID:2164119
Abstract

We studied the cells from three selected patients with Ph-chromosome-negative chronic myeloid leukemia (CML) by Southern blotting, polymerase chain reaction, and in situ hybridization of informative probes to metaphase chromosomes. All three patients had rearrangement of M-BCR sequences in the BCR gene and expression of one or other of the mRNA species characteristic of Ph-positive CML. Leukemic metaphases studied after trypsin-Giemsa banding were indistinguishable from normal. The ABL probe localized both to chromosome 9 and 22 in each case. A probe containing 3' M-BCR sequences localized only to chromosome 22, and not to chromosome 9 as would be expected in Ph-positive CML. Two new probes that recognize different polymorphic regions distal to the ABL gene on chromosome 9 in normal subjects localized exclusively to chromosome 9 in two patients and to both chromosomes 9 and 22 in one patient. These results show that Ph-negative CML with BCR rearrangement is associated with insertion of a variable quantity of chromosome 9 derived material into chromosome 22q11; there is no evidence for reciprocal translocation of material from chromosome 22 to chromosome 9.

摘要

相似文献

1
Interstitial insertion of varying amounts of ABL-containing genetic material into chromosome 22 in Ph-negative CML.
Leukemia. 1990 Apr;4(4):273-7.
2
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Molecular characterization of a variant Ph1 translocation t(9;22;11) (q34;q11;q13) in chronic myelogenous leukemia (CML) reveals the translocation of the 3'-part of BCR gene to the chromosome band 11q13.慢性髓性白血病(CML)中一种变异的费城染色体1易位t(9;22;11) (q34;q11;q13)的分子特征显示,BCR基因的3'端部分易位至染色体带11q13。 1 费城染色体(Philadelphia chromosome,Ph)是一种特异性染色体异常,在慢性髓性白血病中常见。
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Chronic myeloid leukemia with insertion-derived BCR-ABL1 fusion: redefining complex chromosomal abnormalities by correlation of FISH and karyotype predicts prognosis.伴有插入衍生 BCR-ABL1 融合的慢性髓性白血病:通过 FISH 和核型相关性来重新定义复杂染色体异常可预测预后。
Mod Pathol. 2020 Oct;33(10):2035-2045. doi: 10.1038/s41379-020-0564-6. Epub 2020 May 13.
3
Persistence of derivative chromosome 22 after achieving a major molecular response in chronic myeloid leukemia with a cryptic BCR-ABL1 fusion gene.
慢性髓性白血病中隐匿性 BCR-ABL1 融合基因导致达到主要分子缓解后衍生染色体 22 的持续存在。
Int J Hematol. 2009 Dec;90(5):623-626. doi: 10.1007/s12185-009-0448-5. Epub 2009 Dec 10.
4
Molecular analysis of the Philadelphia chromosome.费城染色体的分子分析
Chromosoma. 1991 Sep;100(8):479-86. doi: 10.1007/BF00352198.