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鉴定在急性髓系白血病发病机制中与Cbfb-MYH11协同作用的基因。

Identification of genes that synergize with Cbfb-MYH11 in the pathogenesis of acute myeloid leukemia.

作者信息

Castilla L H, Perrat P, Martinez N J, Landrette S F, Keys R, Oikemus S, Flanegan J, Heilman S, Garrett L, Dutra A, Anderson S, Pihan G A, Wolff L, Liu P P

机构信息

Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):4924-9. doi: 10.1073/pnas.0400930101. Epub 2004 Mar 24.

Abstract

Acute myeloid leukemia subtype M4 with eosinophilia is associated with a chromosome 16 inversion that creates a fusion gene CBFB-MYH11. We have previously shown that CBFB-MYH11 is necessary but not sufficient for leukemogenesis. Here, we report the identification of genes that specifically cooperate with CBFB-MYH11 in leukemogenesis. Neonatal injection of Cbfb-MYH11 knock-in chimeric mice with retrovirus 4070A led to the development of acute myeloid leukemia in 2-5 months. Each leukemia sample contained one or a few viral insertions, suggesting that alteration of one gene could be sufficient to synergize with Cbfb-MYH11. The chromosomal position of 67 independent retroviral insertion sites (RISs) was determined, and 90% of the RISs mapped within 10 kb of a flanking gene. In total, 54 candidate genes were identified; six of them were common insertion sites (CISs). CIS genes included members of a zinc finger transcription factors family, Plag1 and Plagl2, with eight and two independent insertions, respectively. CIS genes also included Runx2, Myb, H2T24, and D6Mm5e. Comparison of the remaining 48 genes with single insertion sites with known leukemia-associated RISs indicated that 18 coincide with known RISs. To our knowledge, this retroviral genetic screen is the first to identify genes that cooperate with a fusion gene important for human myeloid leukemia.

摘要

伴有嗜酸性粒细胞增多的急性髓系白血病M4亚型与16号染色体倒位有关,该倒位产生融合基因CBFB-MYH11。我们之前已表明,CBFB-MYH11对于白血病发生是必要的,但并不充分。在此,我们报告了在白血病发生过程中与CBFB-MYH11特异性协同作用的基因的鉴定。用逆转录病毒4070A对Cbfb-MYH11基因敲入嵌合小鼠进行新生期注射,可导致在2至5个月内发生急性髓系白血病。每个白血病样本含有一个或几个病毒插入位点,这表明改变一个基因可能足以与Cbfb-MYH11协同作用。确定了67个独立逆转录病毒插入位点(RIS)的染色体位置,90%的RIS定位于侧翼基因的10 kb范围内。总共鉴定出54个候选基因;其中6个是常见插入位点(CIS)。CIS基因包括一个锌指转录因子家族的成员Plag1和Plagl2,分别有8个和2个独立插入位点。CIS基因还包括Runx2、Myb、H2T24和D6Mm5e。将其余48个具有单个插入位点的基因与已知白血病相关RIS进行比较,结果表明有18个与已知RIS一致。据我们所知,这种逆转录病毒基因筛选是首次鉴定出与对人类髓系白血病重要的融合基因协同作用的基因。

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