A Higher-Order Complex Containing AF4 and ENL Family Proteins with P-TEFb Facilitates Oncogenic and Physiologic MLL-Dependent Transcription

被引:289
作者
Yokoyama, Akihiko [1 ]
Lin, Min [2 ]
Naresh, Alpana [2 ]
Kitabayashi, Issay [1 ]
Cleary, Michael L. [2 ]
机构
[1] Natl Canc Ctr, Div Mol Oncol, Tokyo 1040045, Japan
[2] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
MIXED-LINEAGE LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; HISTONE METHYLTRANSFERASE COMPLEX; PROTO-ONCOPROTEIN MLL; MYELOID PROGENITORS; CHROMOSOMAL TRANSLOCATIONS; H3K79; METHYLATION; AF4-RELATED GENE; NUCLEAR-PROTEIN; FUSION PARTNERS;
D O I
10.1016/j.ccr.2009.12.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
AF4 and ENL family proteins are frequently fused with MLL, and they comprise a higher order complex (designated AEP) containing the P-TEFb transcription elongation factor. Here, we show that AEP is normally recruited to MLL-target chromatin to facilitate transcription. In contrast, MLL oncoproteins fused with AEP components constitutively form MLL/AEP hybrid complexes to cause sustained target gene expression, which leads to transformation of hematopoietic progenitors. Furthermore, MLL-AF6, an MLL fusion with a cytoplasmic protein, does not form such hybrid complexes, but nevertheless constitutively recruits AEP to target chromatin via unknown alternative mechanisms. Thus, AEP recruitment is an integral part of both physiological and pathological MLL-dependent transcriptional pathways. Bypass of its normal recruitment mechanisms is the strategy most frequently used by MLL oncoproteins.
引用
收藏
页码:198 / 212
页数:15
相关论文
共 58 条
[1]   Binding to nonmethylated CpG DNA is essential for target recognition, transactivation, and myeloid transformation by an MLL oncoprotein [J].
Ayton, PM ;
Chen, EH ;
Cleary, ML .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (23) :10470-10478
[2]   Transformation of myeloid progenitors by MLL oncoproteins is dependent on Hoxa7 and Hoxa9 [J].
Ayton, PM ;
Cleary, ML .
GENES & DEVELOPMENT, 2003, 17 (18) :2298-2307
[3]   The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling [J].
Bitoun, Emmanuelle ;
Oliver, Peter L. ;
Davies, Kay E. .
HUMAN MOLECULAR GENETICS, 2007, 16 (01) :92-106
[4]   Protein arginine-methyltransferase-dependent oncogenesis [J].
Cheung, Ngai ;
Chan, Li Chong ;
Thompson, Alex ;
Cleary, Michael L. ;
So, Chi Wai Eric .
NATURE CELL BIOLOGY, 2007, 9 (10) :1208-1215
[5]   Mouse Af9 is a controller of embryo patterning, like Mll, whose human homologue fuses with AF9 after chromosomal translocation in leukemia [J].
Collins, EC ;
Appert, A ;
Ariza-McNaughton, L ;
Pannell, R ;
Yamada, Y ;
Rabbitts, TH .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (20) :7313-7324
[6]   Similar MLL-associated leukemias arising from self-renewing stem cells and short-lived myeloid progenitors [J].
Cozzio, A ;
Passegué, E ;
Ayton, PM ;
Karsunky, H ;
Cleary, ML ;
Weissman, IL .
GENES & DEVELOPMENT, 2003, 17 (24) :3029-3035
[7]   Extending the repertoire of the mixed-lineage leukemia gene MLL in leukemogenesis [J].
Daser, A ;
Rabbitts, TH .
GENES & DEVELOPMENT, 2004, 18 (09) :965-974
[8]   The AF10 leucine zipper is required for leukemic transformation of myeloid progenitors by MLL-AF10 [J].
DiMartino, JF ;
Ayton, PM ;
Chen, EH ;
Naftzger, CC ;
Young, BD ;
Cleary, ML .
BLOOD, 2002, 99 (10) :3780-3785
[9]   A carboxy-terminal domain of ELL is required and sufficient for immortalization of myeloid progenitors by MLL-ELL [J].
DiMartino, JF ;
Miller, T ;
Ayton, PM ;
Landewe, T ;
Hess, JL ;
Cleary, ML ;
Shilatifard, A .
BLOOD, 2000, 96 (12) :3887-3893
[10]   ACUTE MIXED-LINEAGE LEUKEMIA T(4-11)(Q21-Q23) GENERATES AN MLL-AF4 FUSION PRODUCT [J].
DOMER, PH ;
FAKHARZADEH, SS ;
CHEN, CS ;
JOCKEL, J ;
JOHANSEN, L ;
SILVERMAN, GA ;
KERSEY, JH ;
KORSMEYER, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7884-7888