Zeilinger S, Haller M, Mach R, Kubicek C P
Section Microbial Biochemistry, Institute of Biochemical Technology and Microbiology, Technical University of Vienna, Getreidemarkt 9, Wien, A-1060, Austria.
Biochem Biophys Res Commun. 2000 Nov 2;277(3):581-8. doi: 10.1006/bbrc.2000.3726.
The "cbh2 activating element," CAE, consisting of two separate boxes (ATTGG = CCAAT and GTAATA, respectively) is essential for cellobiohydrolase II gene expression in the filamentous fungus Hypcrea jecorina. Here we report that cell-free extracts from a cellulase-negative mutant form CAE-protein complexes with higher mobility and lower binding-strength compared to the wild type. EMSA analysis demonstrated an increased mobility of the GTAATA-binding protein complex and, supported by in vivo footprinting, a lowered binding strength of the HAP2/3/5 proteins. However, the hap2/hap3/hap5 genes of the mutant are unaltered and transcribed normally. A nucleotide fragment of the cbh1 promoter containing a (GG)CTAATA motif without an adjacent CCAAT box is also bound by cell-free extracts of H. jecorina, and the protein-DNA complex of the mutant shows the characteristic increase in mobility. We conclude that this mutant is defective in the functional formation of the CAE-protein complexes but not in their binding to the target sequences itself.
由两个独立的框(分别为ATTGG = CCAAT和GTAATA)组成的“cbh2激活元件”(CAE)对于丝状真菌里氏木霉中纤维二糖水解酶II基因的表达至关重要。在此我们报告,与野生型相比,纤维素酶阴性突变体的无细胞提取物形成迁移率更高、结合强度更低的CAE - 蛋白质复合物。电泳迁移率变动分析(EMSA)表明GTAATA结合蛋白复合物的迁移率增加,并且在体内足迹法的支持下,HAP2/3/5蛋白的结合强度降低。然而,该突变体的hap2/hap3/hap5基因未改变且转录正常。里氏木霉的无细胞提取物也能结合含有(GG)CTAATA基序但没有相邻CCAAT框的cbh1启动子的核苷酸片段,并且该突变体的蛋白质 - DNA复合物显示出迁移率的特征性增加。我们得出结论,该突变体在CAE - 蛋白质复合物的功能形成方面存在缺陷,但在它们与靶序列本身的结合方面没有缺陷。