Romeo J M, Zusman D R
Department of Molecular and Cell Biology, University of California, Berkeley 94720.
J Bacteriol. 1991 May;173(9):2969-76. doi: 10.1128/jb.173.9.2969-2976.1991.
Myxobacterial hemagglutinin (MBHA) is a major developmentally induced protein that accumulates during the period of cellular aggregation of the fruiting bacterium Myxococcus xanthus. In this study, DNA sequences mediating the transcriptional regulation of mbhA have been identified. Examination of nucleotide sequences upstream of the start site for mbhA transcription has indicated a region of DNA that bears strong homology to the consensus sequence for promoters recognized by the sigma 54 holoenzyme form of RNA polymerase of Escherichia coli and other eubacteria. Deletion of this sequence completely abolished mbhA transcription. Additionally, a cis-acting DNA element, affecting the efficiency of mbhA transcription, has been mapped within a region of DNA 89 to 276 nucleotides upstream of the sigma 54-like sequence. Transposon insertions, mapping within the cis element, drastically reduced mbhA transcriptional activity. These observations suggest that transcription of mbhA requires a productive interaction between a form of RNA polymerase that recognizes a sigma 54-like sequence and a transcriptional activator that binds to DNA sequences upstream of the mbhA promoter.
粘细菌血凝素(MBHA)是一种主要在发育过程中诱导产生的蛋白质,在粘球菌形成子实体的细胞聚集期积累。在本研究中,已鉴定出介导mbhA转录调控的DNA序列。对mbhA转录起始位点上游核苷酸序列的检查表明,有一段DNA区域与大肠杆菌和其他真细菌的RNA聚合酶σ54全酶形式识别的启动子共有序列具有高度同源性。删除该序列完全消除了mbhA转录。此外,一个影响mbhA转录效率的顺式作用DNA元件已被定位在类σ54序列上游89至276个核苷酸的DNA区域内。位于顺式元件内的转座子插入显著降低了mbhA转录活性。这些观察结果表明,mbhA转录需要识别类σ54序列的RNA聚合酶形式与结合在mbhA启动子上游DNA序列的转录激活因子之间进行有效的相互作用。