Chen Yun, Leal Alejandro D, Patel Sejal, Gorski David H
Division of Surgical Oncology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, The Cancer Institute of New Jersey, New Brunswick, New Jersey 088901, USA.
J Biol Chem. 2007 Jan 5;282(1):507-17. doi: 10.1074/jbc.M606604200. Epub 2006 Oct 30.
Tumors secrete pro-angiogenic factors to induce the ingrowth of blood vessels from the surrounding stroma, the end targets of which are vascular endothelial cells (ECs). The homeobox gene GAX inhibits angiogenesis and induces p21(WAF1/CIP1) expression in vascular ECs. To elucidate the mechanism through which GAX activates p21(WAF1/CIP1) expression, we constructed GAX cDNAs with deletions of the N-terminal domain, the homeodomain, or the C-terminal domain and then assessed these constructs for their ability to activate p21(WAF1/CIP1). There was an absolute requirement for the homeodomain, whereas deleting the C-terminal domain decreased but did not abolish transactivation of the p21(WAF1/CIP1) promoter by GAX. Deleting the N-terminal domain did abolish transactivation. Next, we performed chromatin immunoprecipitation and found, approximately 15 kb upstream of the p21(WAF1/CIP1) ATG codon, an ATTA-containing GAX-binding site (designated A6) with a sequence similar to that of other homeodomain-binding sites. GAX was able to bind to A6 in a homeodomain-dependent manner and thereby activate the expression of a reporter gene coupled to this sequence, and this activation was abolished by mutating specific residues in this sequence. On the basis of the sequence of A6, we were then able to locate other ATTA-containing sequences that also bound GAX and activated transcription in reporter constructs. Finally, we found that the ability of these GAX deletions to induce G(0)/G(1) arrest correlates with their ability to transactivate the p21(WAF1/CIP1) promoter. We conclude that GAX activates p21(WAF1/CIP1) through multiple upstream AT-rich sequences. Given the multiple biological activities of GAX in regulating EC function, identification of a putative GAX-binding site will allow the study of how GAX activates or represses other downstream targets to inhibit angiogenesis.
肿瘤分泌促血管生成因子以诱导周围基质中的血管向内生长,其最终作用靶点是血管内皮细胞(ECs)。同源盒基因GAX抑制血管生成并在血管内皮细胞中诱导p21(WAF1/CIP1)表达。为了阐明GAX激活p21(WAF1/CIP1)表达的机制,我们构建了缺失N端结构域、同源结构域或C端结构域的GAX cDNA,然后评估这些构建体激活p21(WAF1/CIP1)的能力。结果发现,绝对需要同源结构域,而删除C端结构域会降低但不会消除GAX对p21(WAF1/CIP1)启动子的反式激活作用。删除N端结构域则确实消除了反式激活作用。接下来,我们进行了染色质免疫沉淀,发现在p21(WAF1/CIP1)ATG密码子上游约15 kb处,有一个含ATTA的GAX结合位点(命名为A6),其序列与其他同源结构域结合位点的序列相似。GAX能够以同源结构域依赖的方式与A6结合,从而激活与该序列偶联的报告基因的表达,并且通过突变该序列中的特定残基可消除这种激活作用。基于A6的序列,我们随后能够定位其他也与GAX结合并在报告基因构建体中激活转录的含ATTA序列。最后,我们发现这些GAX缺失诱导G(0)/G(1)期阻滞的能力与其反式激活p21(WAF1/CIP1)启动子的能力相关。我们得出结论,GAX通过多个上游富含AT的序列激活p21(WAF1/CIP1)。鉴于GAX在调节内皮细胞功能方面具有多种生物学活性,确定一个假定的GAX结合位点将有助于研究GAX如何激活或抑制其他下游靶点以抑制血管生成。