Runx1, c-Myb, and C/EBPα couple differentiation to proliferation or growth arrest during hermatopoiesis

被引:27
作者
Friedman, AD [1 ]
机构
[1] Johns Hopkins Univ, Dept Pediat Oncol, Baltimore, MD 21231 USA
关键词
Runxl; C/EBP alpha; c-Myb; hematopoiesis; cell cycle;
D O I
10.1002/jcb.10271
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
Immature hematopoietic precursors proliferate as they differentiate, whereas terminal differentiation is associated with cell cycle arrest. Stem cell lineage commitment and subseqent maturation is regulated predominantly by transcription factors. Runx1 and c-Myb act in early stage hematopoietic cells to both stimulate proliferation and differentiation, whereas C/EBPalpha, and perhaps other C/EBP family members, block progression from G1 to S and induce terminal maturation. Coupling of differentiation to either proliferation or growth arrest by transcription factors is likely an important regulatory mechanism in multiple developmental systems. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:624 / 629
页数:6
相关论文
共 46 条
[1]   ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain [J].
Amann, JM ;
Nip, J ;
Strom, DK ;
Lutterbach, B ;
Harada, H ;
Lenny, N ;
Downing, JR ;
Meyers, S ;
Hiebert, SW .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (19) :6470-6483
[2]   AN OLIGOMER COMPLEMENTARY TO C-MYB-ENCODED MESSENGER-RNA INHIBITS PROLIFERATION OF HUMAN MYELOID-LEUKEMIA CELL-LINES [J].
ANFOSSI, G ;
GEWIRTZ, AM ;
CALABRETTA, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3379-3383
[3]   AML1 stimulates G1 to S progression via its transactivation domain [J].
Bernardin, F ;
Friedman, AD .
ONCOGENE, 2002, 21 (20) :3247-3252
[4]  
BERNARDIN F, 2002, IN PRESS CANC RES
[5]  
BIES J, 1995, CELL GROWTH DIFFER, V6, P59
[6]   Core binding factor cannot synergistically activate the myeloperoxidase proximal enhancer in immature myeloid cells without c-Myb [J].
BritosBray, M ;
Friedman, AD .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5127-5135
[7]   Dichotomy of AML1-ETO functions: Growth arrest versus block of differentiation [J].
Burel, SA ;
Harakawa, N ;
Zhou, LM ;
Pabst, T ;
Tenen, DG ;
Zhang, DE .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (16) :5577-5590
[8]   CBF beta-SMMHC, expressed in M4Eo AML, reduced CBF DNA-binding and inhibited the G1 to S cell cycle transition at the restriction point in myeloid and lymphoid cells [J].
Cao, WS ;
BritosBray, M ;
Claxton, DF ;
Kelley, CA ;
Speck, NA ;
Liu, PP ;
Friedman, AD .
ONCOGENE, 1997, 15 (11) :1315-1327
[9]   The core binding factor (CBF) α interaction domain and the smooth muscle myosin heavy chain (SMMHC) segment of CBFβ-SMMHC are both required to slow cell proliferation [J].
Cao, WS ;
Adya, N ;
Britos-Bray, M ;
Liu, PP ;
Friedman, AD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (47) :31534-31540
[10]   Retinoblastoma protein directly interacts with and activates the transcription factor NF-IL6 [J].
Chen, PL ;
Riley, DJ ;
ChenKiang, S ;
Lee, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :465-469