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The mitochondrial transcription and packaging factor Tfam imposes a U-turn on mitochondrial DNA

机译:线粒体转录和包装因子Tfam使线粒体DNA发生掉头

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摘要

Tfam (transcription factor A, mitochondrial), a DNA-binding protein with tandem high-mobility group (HMG)-box domains, has a central role in the expression, maintenance and organization of the mitochondrial genome. It activates transcription from mitochondrial promoters and organizes the mitochondrial genome into nucleoids. Using X-ray crystallography, we show that human Tfam forces promoter DNA to undergo a U-turn, reversing the direction of the DNA helix. Each HMG-box domain wedges into the DNA minor groove to generate two kinks on one face of the DNA. On the opposite face, a positively charged α-helix serves as a platform to facilitate DNA bending. The structural principles underlying DNA bending converge with those of the unrelated HU family proteins, which have analogous architectural roles in organizing bacterial nucleoids. The functional importance of this extreme DNA bending is promoter specific and seems to be related to the orientation of Tfam on the promoters.
机译:Tfam(转录因子A,线粒体)是具有串联高迁移率基团(HMG)-box域的DNA结合蛋白,在线粒体基因组的表达,维持和组织中起着核心作用。它激活线粒体启动子的转录,并将线粒体基因组组织成核苷。使用X射线晶体学,我们表明人类Tfam迫使启动子DNA进行掉头,从而反转DNA螺旋的方向。每个HMG盒结构域都楔入DNA小沟中,从而在DNA的一个面上产生两个纽结。在相反的面上,带正电的α-螺旋充当促进DNA弯曲的平台。 DNA弯曲的基础结构原理与无关的HU家族蛋白的结构原理融合,后者在组织细菌类核苷酸方面具有类似的建筑作用。这种极端的DNA弯曲的功能重要性是启动子特异性的,并且似乎与Tfam在启动子上的方向有关。

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