Yepiskoposyan Hasmik, Egli Dieter, Fergestad Tim, Selvaraj Anand, Treiber Carina, Multhaup Gerd, Georgiev Oleg, Schaffner Walter
Institute of Molecular Biology, University of Zurich CH-8057 Zurich, Switzerland.
Nucleic Acids Res. 2006;34(17):4866-77. doi: 10.1093/nar/gkl606. Epub 2006 Sep 14.
All organisms are confronted with external variations in trace element abundance. To elucidate the mechanisms that maintain metal homeostasis and protect against heavy metal stress, we have determined the transcriptome responses in Drosophila to sublethal doses of cadmium, zinc, copper, as well as to copper depletion. Furthermore, we analyzed the transcriptome of a metal-responsive transcription factor (MTF-1) null mutant. The gene family encoding metallothioneins, and the ABC transporter CG10505 that encodes a homolog of 'yeast cadmium factor' were induced by all three metals. Zinc and cadmium responses have similar features: genes upregulated by both metals include those for glutathione S-transferases GstD2 and GstD5, and for zinc transporter-like proteins designated ZnT35C and ZnT63C. Several of the metal-induced genes that emerged in our study are regulated by the transcription factor MTF-1. mRNA studies in MTF-1 overexpressing or null mutant flies and in silico search for metal response elements (binding sites for MTF-1) confirmed novel MTF-1 regulated genes such as ferritins, the ABC transporter CG10505 and the zinc transporter ZnT35C. The latter was analyzed in most detail; biochemical and genetic approaches, including targeted mutation, indicate that ZnT35C is involved in cellular and organismal zinc efflux and plays a major role in zinc detoxification.
所有生物都面临着微量元素丰度的外部变化。为了阐明维持金属稳态并抵御重金属胁迫的机制,我们确定了果蝇对亚致死剂量的镉、锌、铜以及对铜缺乏的转录组反应。此外,我们分析了金属反应转录因子(MTF-1)缺失突变体的转录组。编码金属硫蛋白的基因家族以及编码“酵母镉因子”同源物的ABC转运蛋白CG10505均被这三种金属诱导。锌和镉的反应具有相似的特征:两种金属上调的基因包括谷胱甘肽S-转移酶GstD2和GstD5以及名为ZnT35C和ZnT63C的锌转运蛋白样蛋白的基因。我们研究中出现的几个金属诱导基因受转录因子MTF-1调控。对MTF-1过表达或缺失突变果蝇的mRNA研究以及对金属反应元件(MTF-1的结合位点)的计算机搜索证实了新的MTF-1调控基因,如铁蛋白、ABC转运蛋白CG10505和锌转运蛋白ZnT35C。对后者进行了最详细的分析;包括靶向突变在内的生化和遗传方法表明,ZnT35C参与细胞和机体的锌外流,并在锌解毒中起主要作用。