Fusion AML1 transcript in a radiation-associated leukemia results in a truncated inhibitory AML1 protein

被引:35
作者
Hromas, R
Busse, T
Carroll, A
Mack, D
Shopnick, R
Zhang, DE
Nakshatri, H
Richkind, K
机构
[1] Indiana Univ, Ctr Canc, Indianapolis, IN 46202 USA
[2] Canc Care Consultants, Las Vegas, NV USA
[3] Scripps Res Inst, La Jolla, CA USA
[4] Genzyme Genet, Santa Fe, NM USA
关键词
D O I
10.1182/blood.V97.7.2168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AML1 is a transcription factor that is essential for normal hematopoietic development. It is the mast frequent target for translocations in acute leukemia. Recently, fluorescence in situ hybridization was used to identify a novel syndrome of radiation-associated secondary acute myelogenous leukemia that had AML1 translocations. Using polymerase chain reaction, the AML1 fusion transcript was isolated from the patient who had a t(19;21) radiation-associated leukemia. The AML1 gene is fused out of frame to chromosome 19 sequences, resulting in a truncated AML protein bearing the DNA binding domain but not the transcriptional activation domain. This fusion AML1 protein functions as an inhibitor of the normal AML1 protein. (Blood. 2001;97:2168-2170) (C) 2001 by The American Society of Hematology.
引用
收藏
页码:2168 / 2170
页数:3
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