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人白血病细胞系K-562中,bcr/abl融合基因在三条标记染色体上广泛扩增并聚集。

Extensive amplification of bcr/abl fusion genes clustered on three marker chromosomes in human leukemic cell line K-562.

作者信息

Wu S Q, Voelkerding K V, Sabatini L, Chen X R, Huang J, Meisner L F

机构信息

Wisconsin Comprehensive Cancer Center, Madison, USA.

出版信息

Leukemia. 1995 May;9(5):858-62.

PMID:7769849
Abstract

Using fluorescence in situ hybridization (FISH), we were able to demonstrate 22-24-fold amplification of the bcr/abl fusion gene in the human leukemic cell line K-562. About 60% of the amplified sequences are localized to a large acrocentric marker chromosome, with another 30% clustered on a small acrocentric chromosome. In addition to these two masked Ph chromosomes, the remaining bcr/abl fusion genes are located on a der(2) distal to band q33. G- and C-banding analysis revealed similar unique banding patterns in both masked Ph chromosomes and suggests that amplification occurred by tandem duplication of the bcr/abl fusion site. Because the number of bcr/abl fusion genes may be increasing over time, it is critical that researchers using K-562 cells should be aware of this extensive amplification.

摘要

利用荧光原位杂交(FISH)技术,我们能够证实在人白血病细胞系K-562中,bcr/abl融合基因有22 - 24倍的扩增。大约60%的扩增序列定位于一条大的近端着丝粒标记染色体上,另外30%聚集在一条小的近端着丝粒染色体上。除了这两条隐匿的费城染色体(Ph染色体)外,其余的bcr/abl融合基因位于2号染色体q33带远端的衍生染色体der(2)上。G显带和C显带分析显示,两条隐匿的Ph染色体具有相似的独特带型,提示扩增是由bcr/abl融合位点的串联重复所致。由于bcr/abl融合基因的数量可能会随时间增加,使用K-562细胞的研究人员必须意识到这种广泛的扩增现象,这一点至关重要。

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