MOZ-TIF2-induced acute myeloid leukemia requires the MOZ nucleosome binding motif and TIF2-mediated recruitment of CBP

被引:164
作者
Deguchi, K
Ayton, PM
Carapeti, M
Kutok, JL
Snyder, CS
Williams, IR
Cross, NCP
Glass, CK
Cleary, ML
Gilliland, DG
机构
[1] Brigham & Womens Hosp, Div Hematol & Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Harvard Inst Med, Boston, MA 02115 USA
[3] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[4] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[5] Univ Calif San Diego, Dept Med & Cellular & Mol Med, La Jolla, CA 92093 USA
[6] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[7] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
[8] Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
D O I
10.1016/S1535-6108(03)00051-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The MOZ-TIF2 fusion is associated with acute myeloid leukemia (AML) with inv(8)(p11q13). MOZ is a MYST family histone acetyltransferase (HAT), whereas TIF2 is a nuclear receptor coactivator that associates with CREB binding protein (CBP). Here we demonstrate that MOZ-TIF2 has transforming properties in vitro and causes AML in a murine bone marrow transplant assay. The C2HC nucleosome recognition motif of MOZ is essential for transformation, whereas MOZ HAT activity is dispensable. However, MOZ-TIF2 interaction with CBP through the TIF2 CBP interaction domain (CID) is essential for transformation. These results indicate that nucleosomal targeting by MOZ and recruitment of CBP by TIF2 are critical requirements for MOZ-TIF2 transformation and indicate that MOZ gain of function contributes to leukemogenesis.
引用
收藏
页码:259 / 271
页数:13
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