Nørgaard Per, Tachibana Christine, Bruun Anette W, Winther Jakob R
Department of Physiology, Carlsberg Laboratory, Gamle Carlsberg Vej 10, DK-2500 Copenhagen Valby, Denmark.
Yeast. 2003 May;20(7):645-52. doi: 10.1002/yea.978.
We have examined the activities of promoters of a number of yeast genes encoding resident endoplasmic reticulum proteins, and found increased expression in a strain with severe protein disulphide isomerase deficiency. Serial deletion in the promoter of the MPD1 gene, which encodes a PDI1-homologue, revealed a cis-acting element responding to deficiency of protein disulphide isomerase activity (designated CERP). The presence of the sequence element is necessary and sufficient for the upregulation in response to disulphide isomerase deficiency, as measured by a minimal promoter containing the CERP element. The sequence (GACACG) does not resemble the unfolded protein response element. It is present in the upstream regions of the MPD1, MPD2, KAR2, PDI1 and ERO1 genes.
我们研究了多个编码内质网驻留蛋白的酵母基因启动子的活性,发现在严重缺乏蛋白质二硫键异构酶的菌株中表达增加。编码PDI1同源物的MPD1基因启动子的系列缺失揭示了一个对蛋白质二硫键异构酶活性缺乏作出反应的顺式作用元件(称为CERP)。通过含有CERP元件的最小启动子测量,该序列元件的存在对于响应二硫键异构酶缺乏的上调是必要且充分的。序列(GACACG)与未折叠蛋白反应元件不同。它存在于MPD1、MPD2、KAR2、PDI1和ERO1基因的上游区域。