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Mitochondrial transcription is regulated via an ATP 'sensing' mechanism that couples RNA abundance to respiration

机译:线粒体转录是通过将RNA丰度与呼吸耦合的ATP“传感”机制来调节的

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摘要

The information encoded in both the nuclear and mitochondrial genomes must be coordinately regulated to respond to changes in cellular growth and energy states. Despite identification of the mitochondrial RNA polymerase (mtRNAP) from several organisms, little is known about mitochondrial transcriptional regulation. Studying the shift from fermentation to respiration in Saccharomyces cerevisiae, we have demonstrated a direct correlation between in vivo changes in mitochondrial transcript abundance and in vitro sensitivity of mitochondrial promoters to ATP concentration (K,,ATP). Consistent with the idea that the mtRNAP itself senses in vivo ATP levels, we found that transcript abundance correlates with respiration, but only when coupled to mitochondrial ATP synthesis. In addition, we characterized mutations in the mitochondrial promoter and the mtRNAP accessory factor Mtf1 that alter both in vitro K(m)ATP and in vivo transcription in response to respiratory changes. We propose that shifting cellular pools of ATP coordinately control nuclear and mitochondrial transcription.
机译:必须协调地调节在核和线粒体基因组中编码的信息,以响应细胞生长和能量状态的变化。尽管已从几种生物中鉴定出线粒体RNA聚合酶(mtRNAP),但对线粒体转录调控的了解甚少。研究了酿酒酵母从发酵到呼吸的转变,我们证明了线粒体转录本丰度的体内变化与线粒体启动子对ATP浓度(K ,, ATP)的体外敏感性之间存在直接关系。与mtRNAP本身可检测体内ATP水平的想法一致,我们发现转录本丰度与呼吸相关,但仅在与线粒体ATP合成偶联时才存在。此外,我们表征了线粒体启动子和mtRNAP辅助因子Mtf1中的突变,这些突变可改变体外K(m)ATP和体内转录以响应呼吸变化。我们建议,转移ATP的细胞池协调控制核和线粒体的转录。

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