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Drosophila nuclear factor DREF regulates the expression of the mitochondrial DNA helicase and mitochondrial transcription factor B2 but not the mitochondrial translation factor B1

机译:果蝇核因子DREF调节线粒体DNA解旋酶和线粒体转录因子B2的表达但不调节线粒体翻译因子B1的表达

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摘要

DREF [DRE (DNA replication-related element)-binding factor] controls the transcription of numerous genes in Drosophila, many involved in nuclear DNA (nDNA) replication and cell proliferation, three in mitochondrial DNA (mtDNA) replication and two in mtDNA transcription termination. In this work, we have analysed the involvement of DREF in the expression of the known remaining genes engaged in the minimal mtDNA replication (d-mtDNA helicase) and transcription (the activator d-mtTFB2) machineries and of a gene involved in mitochondrial mRNA translation (d-mtTFB1). We have identified their transcriptional initiation sites and DRE sequences in their promoter regions. Gel-shift and chromatin immunoprecipitation assays demonstrate that DREF interacts in vitro and in vivo with the d-mtDNA helicase and d-mtTFB2, but not with the d-mtTFB1 promoters. Transient transfection assays in Drosophila S2 cells with mutated DRE motifs and truncated promoter regions show that DREF controls the transcription of d-mtDNA helicase and d-mtTFB2, but not that of d-mtTFB1. RNA interference of DREF in S2 cells reinforces these results showing a decrease in the mRNA levels of d-mtDNA helicase and d-mtTFB2 and no changes in those of the d-mtTFB1. These results link the genetic regulation of nuclear DNA replication with the genetic control of mtDNA replication and transcriptional activation in Drosophila.
机译:DREF [DRE(DNA复制相关元件)结合因子]控制果蝇中众多基因的转录,许多基因参与核DNA(nDNA)复制和细胞增殖,其中三个参与线粒体DNA(mtDNA)复制,另外两个参与mtDNA转录终止。在这项工作中,我们分析了DREF与参与最小mtDNA复制(d-mtDNA解旋酶)和转录(活化剂d-mtTFB2)机制的已知剩余基因以及参与线粒体mRNA翻译的基因的表达有关。 (d-mtTFB1)。我们已经确定了它们的启动子区域中的转录起始位点和DRE序列。凝胶移位和染色质免疫沉淀试验表明,DREF在体外和体内与d-mtDNA解旋酶和d-mtTFB2相互作用,但不与d-mtTFB1启动子相互作用。在果蝇S2细胞中具有突变的DRE基序和截短的启动子区域的瞬时转染测定表明,DREF控制d-mtDNA解旋酶和d-mtTFB2的转录,但不控制d-mtTFB1的转录。 DREF对S2细胞的RNA干扰增强了这些结果,表明d-mtDNA解旋酶和d-mtTFB2的mRNA水平下降,而d-mtTFB1的mRNA水平没有变化。这些结果将果蝇中核DNA复制的遗传调控与mtDNA复制和转录激活的遗传控制联系起来。

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