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21号染色体特异性酵母人工染色体的DNA序列可检测急性髓性白血病的t(8;21)断点。

DNA sequences of chromosome 21-specific YAC detect the t(8;21) breakpoint of acute myelogenous leukemia.

作者信息

Kearney L, Watkins P C, Young B D, Sacchi N

机构信息

Department of Medical Oncology, Imperial Cancer Research Fund, London, England.

出版信息

Cancer Genet Cytogenet. 1991 Nov;57(1):109-19. doi: 10.1016/0165-4608(91)90196-2.

Abstract

The t(8;21)(q22;q22) is a nonrandom translocation specifically marking blasts of acute myelogenous leukemia (AML) with undifferentiated phenotype. The breakpoint on chromosome 21 involved by this rearrangement has been precisely localized relative to cloned DNA markers by physical and genetic linkage analysis enabling the use of positional cloning for its isolation. Yeast artificial chromosome (YAC) clones for loci proximal (D21S65) and distal (ERG) to the (21q22) breakpoint have been developed and their chromosome 21 origin and location relative to the breakpoint has been established. By using in situ hybridization analysis, a 240 kb YAC clone for the D21S65 locus clearly identified both derivative chromosomes of the (8;21) translocation in metaphase spreads of leukemia blasts with the rearrangement. The characterization of the DNA sequences contained in this 240 kb YAC can reveal the functional consequences of their derangement in leukemia with abnormalities of the (21q22) region.

摘要

t(8;21)(q22;q22)是一种非随机易位,专门标记具有未分化表型的急性髓性白血病(AML)原始细胞。通过物理和遗传连锁分析,已将这种重排所涉及的21号染色体上的断点相对于克隆的DNA标记物精确定位,从而能够使用定位克隆法对其进行分离。已开发出针对(21q22)断点近端(D21S65)和远端(ERG)位点的酵母人工染色体(YAC)克隆,并确定了它们在21号染色体上的起源以及相对于断点的位置。通过原位杂交分析,一个针对D21S65位点的240 kb YAC克隆在具有该重排的白血病原始细胞中期铺片中清晰地识别出了(8;21)易位的两条衍生染色体。对这个240 kb YAC中所含DNA序列的表征可以揭示其在(21q22)区域异常的白血病中发生紊乱的功能后果。

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