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Suppression of Expression Between Adjacent Genes Within Heterologous Modules in Yeast

机译:酵母异源模块内相邻基因之间的表达抑制

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摘要

Recent studies have shown that proximal arrangement of multiple genes can have complex effects on gene expression. For example, in the case of heterologous gene expression modules, certain arrangements of the selection marker and the gene expression cassette may have unintended consequences that limit the predictability and interpretability of module behaviors. The relationship between arrangement and expression has not been systematically characterized within heterologous modules to date. In this study, we quantitatively measured gene expression patterns of the selection marker (KlURA3 driven by the promoter, pKlURA) and the gene expression cassette (GFP driven by the galactose-inducible promoter, pGAL1) in all their possible relative arrangements in Saccharomyces cerevisiae. First, we observed that pKlURA activity depends strongly on the relative arrangement and the activity of pGAL1. Most notably, we observed transcriptional suppression in the case of divergent arrangements: pKlURA activity was reduced when pGAL1 was inactive. Based on our nucleosome occupancy data, we attribute the observed transcriptional reduction to nucleosome repositioning. Second, we observed that pGAL1 activity also depends on the relative arrangement of pKlURA. In particular, strains with divergent promoters showed significantly different pGAL1 activation patterns from other strains, but only when their growth was compromised by lack of uracil. We reasoned that this difference in pGAL1 activation patterns arises from arrangement-dependent pKlURA activity that can affect the overall cell physiology (i.e., cell growth and survival in the uracil-depleted condition). Our results underscore the necessity to consider ramifications of promoter arrangement when using synthetic gene expression modules.
机译:最近的研究表明,多个基因的近端排列可能会对基因表达产生复杂影响。例如,在异源基因表达模块的情况下,选择标记和基因表达盒的某些排列可能会产生意想不到的后果,从而限制了模块行为的可预测性和可解释性。迄今为止,在异源模块中尚未系统地表征排列和表达之间的关系。在这项研究中,我们定量测量了酿酒酵母中所有可能的相对排列的选择标记(由启动子驱动的KlURA3,pKlURA)和基因表达盒(由半乳糖诱导型启动子,pGAL1驱动的GFP)的基因表达模式。首先,我们观察到pKlURA活性很大程度上取决于pGAL1的相对排列和活性。最值得注意的是,我们观察到在不同排列情况下的转录抑制:当pGAL1失活时,pKlURA活性降低。基于我们的核小体占用数据,我们将观察到的转录减少归因于核小体重新定位。其次,我们观察到pGAL1的活性还取决于pKlURA的相对排列。特别是,具有不同启动子的菌株显示出与其他菌株明显不同的pGAL1激活模式,但仅当其生长因缺乏尿嘧啶而受到损害时。我们推断pGAL1激活模式的这种差异是由与排列有关的pKlURA活性引起的,该活性可能影响总体细胞生理(即尿嘧啶耗尽状态下的细胞生长和存活)。我们的结果强调了在使用合成基因表达模块时必须考虑启动子排列的后果。

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