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A novel function of the mitochondrial transcription factor Mtf1 in fission yeast; Mtf1 regulates the nuclear transcription of srk1

机译:线粒体转录因子Mtf1在裂变酵母中的新功能; Mtf1调节srk1的核转录

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摘要

In eukaryotic cells, Mtf1 and its homologues function as mitochondrial transcription factors for the mitochondrial RNA polymerase in the mitochondrion. Here we show that in fission yeast Mtf1 exerts a non-mitochondrial function as a nuclear factor that regulates transcription of srk1, which is a kinase involved in the stress response and cell cycle progression. We first found Mtf1 expression in the nucleus. A ChIP-chip approach identified srk1 as a putative Mtf1 target gene. Over expression of Mtf1 induced transcription of the srk1 gene and Mtf1 deletion led to a reduction in transcription of the srk1 gene in vivo. Mtf1 overexpression causes cell elongation in a srk1 dependent manner. Mtf1 overexpression can cause cytoplasmic accumulation of Cdc25. We also provide biochemical evidence that Mtf1 binds to the upstream sequence of srk1. This is the first evidence that a mitochondrial transcription factor Mtf1 can regulate a nuclear gene. Mtf1 may also have a role in cell cycle progression.
机译:在真核细胞中,Mtf1及其同源物充当线粒体中线粒体RNA聚合酶的线粒体转录因子。在这里,我们显示在裂变酵母中,Mtf1发挥非线粒体功能,作为调节srk1转录的核因子,srk1是参与应激反应和细胞周期进程的激酶。我们首先在细胞核中发现了Mtf1表达。 ChIP芯片方法确定srk1为推定的Mtf1靶基因。 Mtf1的过度表达诱导srk1基因的转录和Mtf1缺失导致体内srk1基因的转录减少。 Mtf1过度表达导致细胞伸长以srk1依赖的方式。 Mtf1过表达会导致Cdc25的细胞质积累。我们还提供Mtf1绑定到srk1上游序列的生化证据。这是线粒体转录因子Mtf1可以调节核基因的第一个证据。 Mtf1也可能在细胞周期进程中起作用。

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