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首页> 外文期刊>Journal of bacteriology >Promoters for Chlamydia Type III Secretion Genes Show a Differential Response to DNA Supercoiling That Correlates with Temporal Expression Pattern
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Promoters for Chlamydia Type III Secretion Genes Show a Differential Response to DNA Supercoiling That Correlates with Temporal Expression Pattern

机译:衣原体III型分泌基因的启动子显示对与时间表达模式相关的DNA超螺旋的差异反应

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Type III secretion (T3S) is important for the establishment and maintenance of a chlamydial infection. The genes encoding T3S components in Chlamydia are transcribed as separate temporal classes, but the mechanisms that regulate the timing of their expression are not understood. In this study, we demonstrate that promoters for 10 predicted T3S transcriptional units are each transcribed in vitro by the major form of chlamydial RNA polymerase but not by an alternative form of RNA polymerase containing σ28. Since changes in DNA supercoiling during chlamydial development have been proposed as a mechanism for temporal gene regulation, we examined the in vitro response of T3S promoters to altered superhelical density. Promoters for three T3S genes that are upregulated at mid times were activated in response to increased DNA supercoiling. In contrast, promoters for three late T3S genes were not sensitive to changes in superhelical density. This differential response to changes in DNA topology is similar to the pattern that has been reported for representative mid and late chlamydial genes that are unrelated to the T3S system. Based on these results, we propose that the temporal expression of T3S genes in Chlamydia is controlled by general mechanisms that regulate σ66-dependent gene expression during the developmental cycle. Our results are consistent with a model in which T3S genes that are upregulated in mid cycle are activated together with other mid genes in response to increased DNA supercoiling.
机译:III型分泌物(T3S)对于衣原体感染的建立和维持很重要。在衣原体中编码T3S成分的基因被转录为单独的时间类别,但尚不清楚调节其表达时间的机制。在这项研究中,我们证明了10个预测的T3S转录单位的启动子分别通过衣原体RNA聚合酶的主要形式在体外转录,而不是通过包含σ 28 < / sup>。由于衣原体发育过程中DNA超螺旋的变化已被提出作为时间基因调控的机制,我们研究了T3S启动子对改变的超螺旋密度的体外响应。响应于DNA超螺旋的增加,激活了在中期正被上调的三个T3S基因的启动子。相反,三个晚期T3S基因的启动子对超螺旋密度的变化不敏感。这种对DNA拓扑变化的差异响应类似于已报道的与T3S系统无关的中,晚期衣原体基因的模式。基于这些结果,我们提出<3>衣原体中T3S基因的时间表达受发育过程中调节σ 66 依赖性基因表达的一般机制的控制。我们的结果与一个模型一致,在该模型中,响应于DNA超螺旋的增加,中周期中上调的T3S基因与其他中基因一起被激活。

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