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Neisserial Correia Repeat-Enclosed Elements Do Not Influence the Transcription of pil Genes in Neisseria gonorrhoeae and Neisseria meningitidis ▿ †

机译:奈瑟氏球菌重复封闭的元素不影响淋病奈瑟氏球菌和脑膜炎奈瑟氏球菌中pil基因的转录 ▿ †

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摘要

Two human-specific neisserial pathogens, Neisseria gonorrhoeae and Neisseria meningitidis, require the expression of type IV pili (tfp) for initial attachment to the host during infection. However, the mechanisms controlling the assembly and functionality of tfp are poorly understood. It is known that the gonococcal pilE gene, encoding the major subunit, is positively regulated by IHF, a multifunctional DNA binding protein. A neisserial specific repetitive DNA sequence, termed the Correia repeat-enclosed element (CREE) is situated upstream of three pil loci: pilHIJKX (pilH-X), pilGD, and pilF. CREEs have been shown to contain strong promoters, and some CREE variants contain a functional IHF binding site. CREEs might therefore be involved in the regulation of tfp biogenesis in pathogenic Neisseria. Site-directed and deletion mutagenesis on promoter::cat reporter constructs demonstrated that transcription of pilH-X and pilGD is from a σ70 promoter and is independent of the CREE. The insertion of a CREE in the pilF promoter region in N. meningitidis generated a functional σ70 promoter. However, there is also a functional promoter at this position in N. gonorrhoeae, where there is no CREE. These results suggest CREE insertion in these three pil loci does not influence transcription and that IHF does not coordinately regulate tfp biogenesis.
机译:淋病奈瑟氏球菌和脑膜炎奈瑟氏球菌是两种人类特异性的奈瑟氏球菌病原,它们需要表达IV型菌毛(tfp)才能在感染过程中初步附着于宿主。但是,控制tfp的组装和功能的机制了解得很少。众所周知,编码主要亚基的淋球菌pilE基因受到多功能DNA结合蛋白IHF的正调控。称为Correia重复封闭元件(CREE)的奈瑟氏菌特异性重复DNA序列位于三个pil基因座的上游:pilHIJKX(pilH-X),pilGD和pilF。已经显示CREE包含强启动子,并且一些CREE变体包含功能性IHF结合位点。因此,CREEs可能参与了致病性奈瑟氏菌中tfp生物发生的调控。在启动子::猫报道基因构建体上的定点诱变和缺失诱变表明,pilH-X和pilGD的转录来自σ70启动子,并且独立于CREE。在脑膜炎奈瑟氏球菌的pilF启动子区域插入CREE产生了功能性的σ70启动子。但是,淋病奈瑟氏球菌中此位置也有功能性启动子,没有CREE。这些结果表明在这三个pil基因座中插入CREE不会影响转录,并且IHF不能协调调节tfp生物发生。

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