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ets-1与染色质结合的特性及其对血小板因子4基因表达的影响。

Properties of ets-1 binding to chromatin and its effect on platelet factor 4 gene expression.

作者信息

Lu Jun, Pazin Michael J, Ravid Katya

机构信息

Department of Biochemistry, Cancer Center, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

出版信息

Mol Cell Biol. 2004 Jan;24(1):428-41. doi: 10.1128/MCB.24.1.428-441.2004.

Abstract

Ets-1 is important for transcriptional regulation in several hematopoietic lineages, including megakaryocytes. Some transcription factors bind to naked DNA and chromatin with different affinities, while others do not. In the present study we used the megakaryocyte-specific promoters platelet factor 4 (PF4), and glycoprotein IIb (GPIIb) as model systems to explore the properties of Ets-1 binding to chromatin. Chromatin immunoprecipitation assays indicated that Ets-1 binds to proximal regions in the PF4 and GPIIb promoters in vivo. In vitro and in vivo experiments showed that Ets-1 binding to chromatin on lineage-specific promoters does not require lineage-specific factors. Moreover, this binding shows the same order of affinity as the binding to naked DNA and does not require ATP-dependent or Sarkosyl-sensitive factors. The effect of Ets-1 binding on promoter activity was examined using the PF4 promoter as a model. We identified a novel Ets-1 site (at -50), and a novel Sarkosyl-sensitive DNase I-hypersensitive site generated by Ets-1 binding to chromatin, which significantly affect PF4 promoter activity. Taken together, our results suggest a model by which Ets-1 binds to chromatin without the need for lineage-specific accessory factors, and Ets-1 binding induces changes in chromatin and affects transactivation, which are essential for PF4 promoter activation.

摘要

Ets-1对包括巨核细胞在内的多种造血谱系的转录调控至关重要。一些转录因子以不同亲和力结合裸露的DNA和染色质,而另一些则不然。在本研究中,我们使用巨核细胞特异性启动子血小板因子4(PF4)和糖蛋白IIb(GPIIb)作为模型系统,以探索Ets-1与染色质结合的特性。染色质免疫沉淀分析表明,Ets-1在体内与PF4和GPIIb启动子的近端区域结合。体外和体内实验表明,Ets-1与谱系特异性启动子上的染色质结合不需要谱系特异性因子。此外,这种结合显示出与结合裸露DNA相同的亲和力顺序,并且不需要ATP依赖性或对十二烷基肌氨酸敏感的因子。以PF4启动子为模型研究了Ets-1结合对启动子活性的影响。我们鉴定出一个新的Ets-1位点(位于-50处),以及一个由Ets-1与染色质结合产生的新的对十二烷基肌氨酸敏感的DNase I超敏位点,它们显著影响PF4启动子活性。综上所述,我们的结果提出了一个模型,即Ets-1无需谱系特异性辅助因子即可与染色质结合,并且Ets-1结合会诱导染色质变化并影响反式激活,这对PF4启动子激活至关重要。

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