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Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element

机译:线粒体D环末端的DNA复制调控涉及解旋酶TWINKLE和保守的序列元件

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摘要

The majority of mitochondrial DNA replication events are terminated prematurely. The nascent DNA remains stably associated with the template, forming a triple-stranded displacement loop (D-loop) structure. However, the function of the D-loop region of the mitochondrial genome remains poorly understood. Using a comparative genomics approach we here identify two closely related 15 nt sequence motifs of the D-loop, strongly conserved among vertebrates. One motif is at the D-loop 5′-end and is part of the conserved sequence block 1 (CSB1). The other motif, here denoted coreTAS, is at the D-loop 3′-end. Both these sequences may prevent transcription across the D-loop region, since light and heavy strand transcription is terminated at CSB1 and coreTAS, respectively. Interestingly, the replication of the nascent D-loop strand, occurring in a direction opposite to that of heavy strand transcription, is also terminated at coreTAS, suggesting that coreTAS is involved in termination of both transcription and replication. Finally, we demonstrate that the loading of the helicase TWINKLE at coreTAS is reversible, implying that this site is a crucial component of a switch between D-loop formation and full-length mitochondrial DNA replication.
机译:大多数线粒体DNA复制事件都提前终止。新生DNA保持与模板稳定结合,形成三链置换环(D环)结构。但是,线粒体基因组的D环区域的功能仍然知之甚少。使用比较基因组学方法,我们在这里鉴定了两个紧密相关的D环的15 nt序列基序,这些基序在脊椎动物中非常保守。一个基序在D-环5'-末端,是保守序列模块1(CSB1)的一部分。另一个基序,在这里表示为coreTAS,在D环3'末端。这两个序列都可能阻止跨D环区域的转录,因为轻链和重链转录分别终止于CSB1和coreTAS。有趣的是,新生D环链的复制沿与重链转录相反的方向发生,也终止于coreTAS,这表明coreTAS参与转录和复制的终止。最后,我们证明了解旋酶TWINKLE在coreTAS上的加载是可逆的,这意味着该位点是D环形成与全长线粒体DNA复制之间转换的关键组成部分。

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