Liu Yang, Cui Yaya, Mukherjee Asita, Chatterjee Arun K
Department of Plant Pathology, University of Missouri-Columbia, 108 Waters Hall, MO 65211, USA.
Microbiology (Reading). 1997 Mar;143 ( Pt 3):705-712. doi: 10.1099/00221287-143-3-705.
The activation of pectin lyase (Pnl) production in Erwinia carotovora subsp. carotovora strain 71 occurs upon DNA damage via a unique regulatory circuit involving recA, rdgA and rdgB. In a similar Pnl-inducible system reconstituted in Escherichia coli, the rdgB product was found to activate the expression of pnlA, the structural gene for pectin lyase. The kinetic data presented here also show that transcription of pnlA followed that of rdgB in Er. carotovora subsp. carotovora, indicating a temporal order of gene expression. By deletion analysis we have localized the promoter/regulatory region within a 66 bp DNA segment upstream of the pnlA transcriptional start site. This region contains the -10 consensus sequence but not the sequences corresponding to the E. coli -35 region. For DNA-binding studies, rdgB was overexpressed in E. coli and a 14 kDa polypeptide was identified as the gene product. RdgB from crude extracts or a purified preparation caused an identical gel mobility shift of a 164 bp DNA segment containing the pnlA promoter/regulatory region. Utilizing DNase I protection assay the RdgB-binding site was localized between nucleotides -29 and -56, i.e. overlapping the position of the putative -35 box. The findings reported here, taken along with our previous observation that the rdgE product is required for pnlA expression, establishes that rdgB encodes a transcriptional factor which specifically interacts with the pnlA promoter/regulatory region.
胡萝卜软腐欧文氏菌胡萝卜软腐亚种71中果胶裂解酶(Pnl)产量的激活发生在DNA损伤时,通过一个涉及recA、rdgA和rdgB的独特调控回路。在大肠杆菌中重建的类似Pnl诱导系统中,发现rdgB产物可激活果胶裂解酶结构基因pnlA的表达。此处给出的动力学数据还表明,在胡萝卜软腐欧文氏菌胡萝卜软腐亚种中,pnlA的转录跟随rdgB的转录,表明基因表达存在时间顺序。通过缺失分析,我们将启动子/调控区域定位在pnlA转录起始位点上游66 bp的DNA片段内。该区域包含-10共有序列,但不包含与大肠杆菌-35区域对应的序列。为了进行DNA结合研究,rdgB在大肠杆菌中过表达,一种14 kDa的多肽被鉴定为基因产物。来自粗提物或纯化制剂的RdgB导致包含pnlA启动子/调控区域的164 bp DNA片段发生相同的凝胶迁移率变动。利用DNase I保护试验,RdgB结合位点定位在核苷酸-29至-56之间,即与假定的-35框位置重叠。此处报道的研究结果,连同我们之前观察到的pnlA表达需要rdgE产物这一结果,表明rdgB编码一种转录因子,该转录因子与pnlA启动子/调控区域特异性相互作用。