Yamauchi Seiji, Higashitani Nahoko, Otani Mieko, Higashitani Atsushi, Ogura Teru, Yamanaka Kunitoshi
Division of Molecular Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, 2-2-1 Honjo, Kumamoto 860-0811, Japan.
Dev Biol. 2008 Jun 15;318(2):348-59. doi: 10.1016/j.ydbio.2008.02.057. Epub 2008 Mar 13.
Caenorhabditis elegans possesses two p97/VCP/Cdc48p homologues, named CDC-48.1 (C06A1.1) and CDC-48.2 (C41C4.8), and their expression patterns and levels are differently regulated. To clarify the regulatory mechanisms of differential expression of two p97 proteins of C. elegans, we performed detailed deletion analysis of their promoter regions. We found that the promoter of cdc-48.1 contains two regions necessary for embryonic and for post-embryonic expression, while the promoter of cdc-48.2 contains the single region necessary for embryonic expression. In particular, two elements (Element A and Element B) and three conserved boxes (Box a, Box b and Box c) were essential for cdc-48.1 expression in embryos and at post-embryonic stages, respectively. By using South-Western blotting and MALDI-TOF MS analysis, we identified HMG-12 and CAR-1 as proteins that bind to Element A and Element B, respectively, from the embryonic nuclear extract. Importantly, we found the decreased expression of p97 in embryos prepared from hmg-12(RNAi) or car-1(RNAi) worms. These results indicate that both HMG-12 and CAR-1 play important roles in embryonic expression of cdc-48.1.
秀丽隐杆线虫拥有两个p97/VCP/Cdc48p同源物,分别命名为CDC-48.1(C06A1.1)和CDC-48.2(C41C4.8),它们的表达模式和水平受到不同的调控。为了阐明秀丽隐杆线虫两种p97蛋白差异表达的调控机制,我们对它们的启动子区域进行了详细的缺失分析。我们发现,cdc-48.1的启动子包含胚胎期和胚胎后期表达所需的两个区域,而cdc-48.2的启动子只包含胚胎期表达所需的单个区域。特别是,两个元件(元件A和元件B)和三个保守框(框a、框b和框c)分别对胚胎期和胚胎后期cdc-48.1的表达至关重要。通过蛋白质印迹法和基质辅助激光解吸电离飞行时间质谱分析,我们从胚胎核提取物中鉴定出HMG-12和CAR-1分别是与元件A和元件B结合的蛋白质。重要的是,我们发现从hmg-12(RNAi)或car-1(RNAi)线虫制备的胚胎中p97的表达降低。这些结果表明,HMG-12和CAR-1在cdc-48.1的胚胎期表达中都起着重要作用。