PU.1 Directly Regulates cdk6 Gene Expression, Linking the Cell Proliferation and Differentiation Programs in Erythroid Cells

被引:27
作者
Choe, Kevin S. [1 ]
Ujhelly, Olga [1 ]
Wontakal, Sandeep N. [1 ]
Skoultchi, Arthur I. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR PU.1; CYCLIN-DEPENDENT KINASES; TERMINAL DIFFERENTIATION; ERYTHROLEUKEMIA-CELLS; C-MYC; DEREGULATED EXPRESSION; C/EBP-ALPHA; GATA-1; MACROPHAGE; BINDING;
D O I
10.1074/jbc.M109.077727
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
Cell proliferation and differentiation are highly coordinated processes during normal development. Most leukemia cells are blocked from undergoing terminal differentiation and also exhibit uncontrolled proliferation. Dysregulated expression of transcription factor PU.1 is strongly associated with Friend virus-induced erythroleukemia. PU.1 inhibits erythroid differentiation by binding to and inhibiting GATA-1. PU.1 also may be involved in controlling proliferation of erythroid cells. We reported previously that the G(1) phase-specific cyclin-dependent kinase 6 (CDK6) also blocks erythroid differentiation. We now report that PU.1 directly stimulates transcription of the cdk6 gene in both normal erythroid progenitors and erythroleukemia cells, as well as in macrophages. We propose that PU.1 coordinates proliferation and differentiation in immature erythroid cells by inhibiting the GATA-1-mediated gene expression program and also by regulating expression of genes that control progression through the G(1) phase of the cell cycle, the period during which the decision to differentiate is made.
引用
收藏
页码:3044 / 3052
页数:9
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