Chen Hexin, Rubin Ethel, Zhang Huiping, Chung Seung, Jie Charles C, Garrett Elizabeth, Biswal Shyam, Sukumar Saraswati
Breast Cancer Program, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins Hospital, Baltimore, Maryland 21231-1000, USA.
J Biol Chem. 2005 May 13;280(19):19373-80. doi: 10.1074/jbc.M413528200. Epub 2005 Mar 9.
The homeobox gene HOXA5 encodes a transcription factor that has been shown to play important roles in embryogenesis, hematopoiesis, and tumorigenesis. In order to decipher downstream signaling pathways of HOXA5, we utilized oligonucleotide microarray analysis to identify genes that are differentially expressed in HOXA5-induced cells compared with uninduced cells. Comparative analysis of gene expression changes after 9 h of HOXA5 induction in Hs578T breast cancer cells identified 306 genes whose expression was modulated at least 2-fold. Ten of these 306 genes were also up-regulated by at least 2-fold at 6 h post-induction. The expression of all of these 10 genes was confirmed by semiquantitative reverse transcription-PCR. Among these 10 genes, which are most likely to be direct targets of HOXA5, we initiated an investigation into the pleiotrophin gene by first cloning its promoter. Transient transfection assays indicated that HOXA5 can specifically activate the pleiotrophin promoter. Promoter deletion, chromatin immunoprecipitation assay, and gel-shift assays were performed to show that HOXA5 can directly bind to one binding site on the pleiotrophin promoter. These data strongly suggest that microarray analysis can successfully identify many potential direct downstream genes of HOXA5. Further functional analysis of these targets will allow us to better understand the diverse functions of HOXA5 in embryonic development and tumorigenesis.
同源框基因HOXA5编码一种转录因子,该转录因子已被证明在胚胎发生、造血和肿瘤发生中发挥重要作用。为了解析HOXA5的下游信号通路,我们利用寡核苷酸微阵列分析来鉴定与未诱导细胞相比,在HOXA5诱导的细胞中差异表达的基因。对Hs578T乳腺癌细胞中HOXA5诱导9小时后的基因表达变化进行比较分析,鉴定出306个表达至少被调节2倍的基因。这306个基因中的10个在诱导后6小时也至少上调了2倍。通过半定量逆转录PCR证实了所有这10个基因的表达。在这10个最有可能是HOXA5直接靶标的基因中,我们首先通过克隆其启动子对多效生长因子基因展开研究。瞬时转染实验表明HOXA5可以特异性激活多效生长因子启动子。进行了启动子缺失、染色质免疫沉淀实验和凝胶迁移实验,以表明HOXA5可以直接结合多效生长因子启动子上的一个结合位点。这些数据有力地表明,微阵列分析可以成功鉴定出许多HOXA5潜在的直接下游基因。对这些靶标的进一步功能分析将使我们能够更好地理解HOXA5在胚胎发育和肿瘤发生中的多种功能。