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截短的Hoxa1蛋白在干细胞中与Hoxa1和Pbx1相互作用。

The truncated Hoxa1 protein interacts with Hoxa1 and Pbx1 in stem cells.

作者信息

Fernandez Cristina C, Gudas Lorraine J

机构信息

Department of Pharmacology, Weill Cornell Medical College, 1300 York Avenue, New York, New York 10065, USA.

出版信息

J Cell Biochem. 2009 Feb 15;106(3):427-43. doi: 10.1002/jcb.22023.

Abstract

Hox genes contain a homeobox encoding a 60-amino acid DNA binding sequence. The Hoxa1 gene (Hox1.6, ERA1) encodes two alternatively spliced mRNAs that encode distinct proteins, one with the homeodomain (Hoxa1-993), and another protein lacking this domain (Hoxa1-399). The functions of Hoxa1-399 are unknown. We detected Hoxa1-993 and Hoxa1-399 by immunoprecipitation using Hoxa1 antibodies. To assess whether Hoxa1-399 functions in cellular differentiation, we analyzed Hoxb1, a Hoxa1 target gene. Hoxa1-993 and its cofactor, Pbx1, bind to the Hoxb1 SOct-R3 promoter to transcriptionally activate a luciferase reporter. Results from F9 stem cells that stably express ectopic Hoxa1-399 (the F9-399 line) show that Hoxa1-399 reduces this transcriptional activation. Gel shift assays demonstrate that Hoxa1-399 reduces Hoxa1-993/Pbx1 binding to the Hoxb1 SOct-R3 region. GST pull-down experiments suggest that Hoxa1-399, Hoxa1-993, and Pbx1 form a trimer. However, the F9-399 line exhibits no differences in RA-induced proliferation arrest or endogenous Hoxb1, Pbx1, Hoxa5, Cyp26a1, GATA4, or Meis mRNA levels when compared to F9 wild-type.

摘要

Hox基因包含一个编码60个氨基酸DNA结合序列的同源异型框。Hoxa1基因(Hox1.6,ERA1)编码两种选择性剪接的mRNA,它们编码不同的蛋白质,一种带有同源结构域(Hoxa1-993),另一种缺乏该结构域的蛋白质(Hoxa1-399)。Hoxa1-399的功能尚不清楚。我们使用Hoxa1抗体通过免疫沉淀检测到了Hoxa1-993和Hoxa1-399。为了评估Hoxa1-399在细胞分化中的功能,我们分析了Hoxa1的靶基因Hoxb1。Hoxa1-993及其辅因子Pbx1与Hoxb1 SOct-R3启动子结合,以转录激活荧光素酶报告基因。稳定表达异位Hoxa1-399的F9干细胞(F9-399系)的结果表明,Hoxa1-399降低了这种转录激活。凝胶迁移实验表明,Hoxa1-399减少了Hoxa1-993/Pbx1与Hoxb1 SOct-R3区域的结合。GST下拉实验表明,Hoxa1-399、Hoxa1-993和Pbx1形成三聚体。然而,与F9野生型相比,F9-399系在视黄酸诱导的增殖停滞或内源性Hoxb1、Pbx1、Hoxa5、Cyp26a1、GATA4或Meis mRNA水平上没有差异。

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