Regulation of gene expression in Borrelia burgdorferi

伯氏疏螺旋体是莱姆病的病原体。B。布格多费里运河 合成参与发病或传播的几种不同的外表面蛋白质 在动物流行周期中。外表面蛋白质合成的调节还不清楚 在分子水平上。本申请提出评估顺式作用因子， 如DNA超螺旋，和反式作用因子，如DNA结合阻遏蛋白， 调节外表面蛋白基因的表达以响应环境信号。 外表面蛋白OspA和OspC的产生是受调节的，这可能是如何 B。burgdorferi适应蜱媒介和哺乳动物宿主的不同环境或影响 环境之间的传播。一种ospAB操纵子启动子特异性反式作用蛋白， 假设抑制ospAB转录。将纯化和鉴定调节蛋白。 假设ospAB启动子区域中的顺式作用序列介导转录调控。 调控将对这些地点进行测绘和定性。建筑DNA结合蛋白 假设Hbb促进ospC表达的调节。探讨血红蛋白的功能 通过hbb基因和ospC启动子区域中的Hbb结合位点的诱变。ospc 启动子将被诱导型启动子系统替换，以控制细胞OspC水平， 扰乱DNA超螺旋，从而可以研究ospC和ospAB转录的偶联。 假定来自flac杂合启动子的ospC基因表达受IPTG调节， 以影响ospAB操纵子表达。DNA超螺旋调控ospC的机制 假设表达涉及Hbb和ospC启动子中的特定序列基序 地区将构建突变体ospC启动子。这些突变体的转录反应 为了确定顺式作用元件， 负责监管。这些研究的长期目标是了解 外表面蛋白基因对环境信号的调控机制。

The bacterium Borrelia burgdorferi is a causative agent of Lyme disease. B. burgdorferi can synthesize several different outer surface proteins that are involved in pathogenesis or transmission during the enzootic cycle. The regulation of outer surface protein synthesis is not well understood at the molecular level. This application proposes to evaluate the hypothesis that cis-acting factors, such as DNA supercoiling, and trans-acting factors, such as DNA-binding repressor proteins, regulate the expression of outer surface protein genes in response to environmental signals. Production of outer surface proteins OspA and OspC is reciprocally regulated, which may be how B. burgdorferi adapts to the different environments of the tick vector and mammalian host or effects transmission between the environments. An ospAB operon promoter-specific trans-acting protein is hypothesized to repress ospAB transcription. The regulatory protein will be purified and identified. Cis-acting sequences in the ospAB promoter region are hypothesized to mediate transcriptional regulation. These sites will be mapped and characterized. The architectural DNA-binding protein Hbb is hypothesized to facilitate regulation of ospC expression. The function of Hbb will be probed by mutagenesis of the hbb gene and the Hbb binding site in the ospC promoter region. The ospC promoter will be replaced with an inducible promoter system to control cellular OspC levels without perturbing DNA supercoiling so that the coupling of ospC and ospAB transcription can be studied. ospC gene expression from the flac hybrid promoter is hypothesized to be regulated by IPTG and to influence ospAB operon expression. The mechanism by which DNA supercoiling regulates ospC expression is hypothesized to involve Hbb and specific sequence motifs in the ospC promoter region. Mutant ospC promoters will be constructed. The transcriptional response of these mutants to temperature and DNA supercoiling will be assayed in order to define the cis-acting elements responsible for regulation. The long-term objective of these studies is to understand the mechanism of outer surface protein gene regulation in response to environmental signals.