Liu E S, Lee A S
Department of Biochemistry, University of Southern California School of Medicine, Los Angeles 90033.
Nucleic Acids Res. 1991 Oct 11;19(19):5425-31. doi: 10.1093/nar/19.19.5425.
The GRP78 and GRP94 are two constitutively expressed ER resident proteins that are coordinately induced in response to stress conditions. The control of their induction is at the transcriptional level. We have previously demonstrated that the GRP78 and the GRP94 promoters share a common regulatory domain which is highly conserved. We report here that within this 36 bp promoter region is a CG/CAAT and a GC-rich sequence motif which are important for basal level and induced expression of the gene. Gel mobility shift assays with HeLa nuclear extracts and the conserved element from GRP78 and GRP94 show two shared, specific protein-DNA complexes. By ultraviolet cross-linking, the sizes of the proteins labeled in the slower-migrating complex are 210-, 110-, a doublet at 90/92- and 70 kD, and in the faster-migrating complex, protein species of about 55 kD. The formation of the second complex can be inhibited by competition with the coding strand of the conserved GRP element in a sequence specific manner. In addition, the Ku autoantigen which is abundant in HeLa cell extracts also binds. The sizes of the nuclear factors binding to the GRP78 and GRP94 conserved promoter elements are strikingly similar, providing further evidence that the two genes are coordinately regulated by common trans-acting factors.
GRP78和GRP94是两种组成型表达的内质网驻留蛋白,在应激条件下会被协同诱导。它们的诱导调控发生在转录水平。我们之前已经证明,GRP78和GRP94启动子共享一个高度保守的共同调控域。我们在此报告,在这个36 bp的启动子区域内有一个CG/CAAT和一个富含GC的序列基序,它们对基因的基础水平和诱导表达很重要。用HeLa细胞核提取物以及GRP78和GRP94的保守元件进行凝胶迁移率变动分析,显示出两个共享的特异性蛋白质-DNA复合物。通过紫外线交联,在迁移较慢的复合物中标记的蛋白质大小为210、110、90/92处的双峰以及70 kD,在迁移较快的复合物中,蛋白质种类约为55 kD。第二个复合物的形成可以通过与保守的GRP元件的编码链进行序列特异性竞争来抑制。此外,HeLa细胞提取物中丰富的Ku自身抗原也会结合。与GRP78和GRP94保守启动子元件结合的核因子大小惊人地相似,这进一步证明这两个基因由共同的反式作用因子协同调控。