Gulati P, Xu D, Kaplan H B
Department of Microbiology and Molecular Genetics, University of Texas Medical School, Houston 77030, USA.
J Bacteriol. 1995 Aug;177(16):4645-51. doi: 10.1128/jb.177.16.4645-4651.1995.
Developmental expression of the Myxococcus xanthus gene 4521 requires extracellular A-signal. This signal is generated in response to nutrient limitation and functions in cell density sensing. To identify the upstream limit of the minimum region required in vivo for A-signal-dependent 4521 expression, a 5' deletion analysis of the 4521 regulatory region was performed. A new vector, pHBK280, was designed to facilitate this analysis. This vector creates tandem copies of the 4521 gene in the M. xanthus chromosome, such that the regulatory region to be tested is upstream of a single copy of the lacZ reporter gene. The 5' deletion analysis revealed that at most, 146 bp of DNA upstream of the transcription start site (TSS) was required for full developmental expression of 4521. Basal expression levels were observed with constructions containing 90 bp of DNA upstream of the TSS. In vitro gel retardation assays revealed that DNA fragments with 5' ends of 146 and 125 bp upstream of the TSS and a common 3' end of +24 bp were retarded in their mobility after incubation with all of the M. xanthus developmental crude cell extracts tested. In contrast, a fragment starting at 90 bp upstream of the TSS and ending at +24 bp was not retarded in its mobility after incubation with the same cell extracts. These in vivo and in vitro data suggest that cis-acting elements located between 146 and 90 bp upstream of the TSS serve as binding sites for one or more trans-acting regulatory factors required for 4521 developmental expression.
黄色粘球菌基因4521的发育表达需要细胞外A信号。该信号是对营养限制作出反应而产生的,并在细胞密度感应中发挥作用。为了确定体内A信号依赖性4521表达所需最小区域的上游界限,对4521调控区域进行了5'缺失分析。设计了一种新载体pHBK280来促进这一分析。该载体在黄色粘球菌染色体中产生4521基因的串联拷贝,使得待测试的调控区域位于lacZ报告基因单拷贝的上游。5'缺失分析表明,转录起始位点(TSS)上游最多146 bp的DNA对于4521的完全发育表达是必需的。在含有TSS上游90 bp DNA的构建体中观察到基础表达水平。体外凝胶阻滞试验表明,TSS上游5'端为146和125 bp且3'端为+24 bp的DNA片段,在与所有测试的黄色粘球菌发育粗细胞提取物孵育后,其迁移率受到阻滞。相比之下,一个从TSS上游90 bp开始并在+24 bp结束的片段,在与相同细胞提取物孵育后,其迁移率没有受到阻滞。这些体内和体外数据表明,位于TSS上游146至90 bp之间的顺式作用元件作为4521发育表达所需的一种或多种反式作用调节因子的结合位点。