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Overlapping activator sequences determined for two oppositely oriented promoters in halophilic Archaea

机译:嗜盐古生菌中两个相反方向启动子的重叠激活序列

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摘要

Transcription of the genomic region involved in gas vesicle formation in Halobacterium salinarum (p-vac) and Haloferax mediterranei (mc-vac) is driven by two divergent promoters, PA and PD, separated by only 35 nt. Both promoters are activated by the transcription activator GvpE which in the case of PmcA requires a 20-nt sequence (UAS) consisting of two conserved 8-nt sequence portions located upstream of BRE. Here, we determined the two UAS elements in the promoter region of p-vac by scanning mutageneses using constructs containing PpD (without PpA) fused to the bgaH reporter gene encoding an enzyme with β-galactosidase activity, or the dual reporter construct pApD with PpD fused to bgaH and PpA to an altered version of gvpA. The two UAS elements found exhibited a similar extension and distance to BRE as previously determined for the UAS in PmcA. Their distal 8-nt portions almost completely overlapped in the centre of PpD–PpA, and mutations in this region negatively affected the GvpE-mediated activation of both promoters. Any alteration of the distance between BRE and UAS resulted in the loss of the GvpE activation, as did a complete substitution of the proximal 8-nt portion, underlining that a close location of UAS and BRE was very important.
机译:唾液盐杆菌(p-vac)和地中海嗜盐菌(haloferax mediterranei)(mc-vac)中参与气体囊泡形成的基因组区域的转录是由两个不同的启动子PA和PD驱动的,它们仅相距35 nt。这两个启动子都被转录激活因子GvpE激活,在PmcA的情况下,它需要一个20-nt序列(UAS),该序列由位于BRE上游的两个保守的8-nt序列组成。在这里,我们通过使用包含与编码具有β-半乳糖苷酶活性的酶的bgaH报告基因融合的PpD(无PpA)的构建体或带有PpD的双重报告子构建体pApD,通过扫描诱变酶来确定p-vac启动子区域中的两个UAS元件。与bgaH和PpA融合为gvpA的变更版本。发现的两个UAS元素显示出与BRE相似的延伸范围和距离,这与先前在PmcA中为UAS确定的相似。它们的远端8-nt部分几乎完全重叠在PpD–PpA的中心,该区域的突变对GvpE介导的两个启动子的激活均产生负面影响。 BRE和UAS之间距离的任何改变都会导致GvpE激活的丧失,近端8-nt部分的完全置换也是如此,这表明UAS和BRE的紧密位置非常重要。

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