ETO interacting proteins

被引:86
作者
Hug, BA
Lazar, MA
机构
[1] Univ Penn, Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Penn Diabet Ctr, Philadelphia, PA 19104 USA
关键词
ETO; MTG8; repression; corepressor; HDAC;
D O I
10.1038/sj.onc.1207674
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 8; 21 translocation produces a fusion between the ETO gene and that encoding the myeloid transcription factor AML1. The AML1-ETO fusion substitutes the majority of the ETO protein for the coregulator recruitment domains of AML1. Biochemical analyses of ETO have led to the identification of numerous interacting proteins including many corepressors. Importantly, the proteins interacting with ETO are different from those of wild-type AML1, suggesting that altered coregulator recruitment underlies the oncogenic properties of AML1 - ETO. The list of corepressors capable of binding ETO includes histone deacetylases (HDACs) and components of distinct HDAC core complexes. These investigations have provided mechanistic insight into corepressor recruitment by ETO and clues to the leukemogenic activity of AML1 - ETO.
引用
收藏
页码:4270 / 4274
页数:5
相关论文
共 50 条
[11]   Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO [J].
Gelmetti, V ;
Zhang, JS ;
Fanelli, M ;
Minucci, S ;
Pelicci, PG ;
Lazar, MA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (12) :7185-7191
[12]   Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis [J].
Gottlieb, PD ;
Pierce, SA ;
Sims, RJ ;
Yamagishi, H ;
Weihe, EK ;
Harriss, JV ;
Maika, SD ;
Kuziel, WA ;
King, HL ;
Olson, EN ;
Nakagawa, O ;
Srivastava, D .
NATURE GENETICS, 2002, 31 (01) :25-32
[13]   DEAF-1, a novel protein that binds an essential region in a Deformed response element [J].
Gross, CT ;
McGinnis, W .
EMBO JOURNAL, 1996, 15 (08) :1961-1970
[14]  
Guenther MG, 2000, GENE DEV, V14, P1048
[15]   The SMRT and N-CoR corepressors are activating cofactors for histone deacetylase 3 [J].
Guenther, MG ;
Barak, O ;
Lazar, MA .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (18) :6091-6101
[16]   Multiple regions of ETO cooperate in transcriptional repression [J].
Hildebrand, D ;
Tiefenbach, J ;
Heinzel, T ;
Grez, M ;
Maurer, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9889-9895
[17]  
Hug BA, 2002, CANCER RES, V62, P2906
[18]   Stable histone deacetylase complexes distinguished by the presence of SANT domain proteins CoREST/kiaa0071 and Mta-L1 [J].
Humphrey, GW ;
Wang, YH ;
Russanova, VR ;
Hirai, T ;
Qin, J ;
Nakatani, Y ;
Howard, BH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6817-6824
[19]  
Hung HL, 1999, MOL CELL BIOL, V19, P3496
[20]   Stimulation of NF-E2 DNA binding by CREB-binding protein (CBP)-mediated acetylation [J].
Hung, HL ;
Kim, AY ;
Hong, W ;
Rakowski, C ;
Blobel, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :10715-10721