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A DNA unwinding factor involved in DNA replication in cell-free extracts of Xenopus eggs

机译:非洲爪蟾卵的无细胞提取物中涉及DNA复制的DNA解旋因子

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Background: Alteration of chromatin structure is a key step in various aspects of DNA metabolism. DNA unwinding factors such as the high mobility group (HMG) proteins are thought to play a general role in controlling chromatin structure and a specific role in controlling DNA replication. For instance, in the in vitro simian virus 40 replication system, minichromosomes containing HMG-17 replicate more efficiently than those without it, suggesting that HMG-17 enhances the rate of replication of a chromatin template by unfolding the higher-order chromatin structure. At present, however, only limited data suggest an involvement of DNA unwinding factors in DNA replication. Results: We purified from Xenopus eggs a novel heterodimeric factor, termed DNA unwinding factor (DUF), that consists of 87 kDa and 140 kDa polypeptides. DUF unwinds closed-circular duplex DNA in the presence of topoisomerase I, but it does not possess a DNA gyrase activity: it does not introduce negative supercoils into DNA at the expense of ATP hydrolysis. Cloning and sequencing of the cDNAs encoding the two polypeptides revealed that the 87 kDa polypeptide is homologous to a mammalian HMG protein, T160/structure-specific recognition protein. The 140 kDa polypeptide is homologous to yeast Cdc68, a protein that controls the expression of several genes during the G1 phase of the cell cycle by modulating chromatin structure. Immunodepletion of DUF from Xenopus egg extracts drastically reduced the ability of the extract to replicate exogenously added sperm chromatin or plasmid DNA. Conclusions: We propose that DUF plays a role in DNA replication in Xenopus egg extracts.
机译:背景:染色质结构的改变是DNA代谢各个方面的关键步骤。人们认为诸如高迁移率族(HMG)蛋白之类的DNA解绕因子在控制染色质结构中起一般作用,而在控制DNA复制中起特定作用。例如,在体外猿猴病毒40复制系统中,含有HMG-17的微型染色体比没有它的微型染色体更有效地复制,这表明HMG-17通过展开较高阶的染色质结构来提高染色质模板的复制速率。然而,目前只有有限的数据表明DNA解旋因子参与DNA复制。结果:我们从非洲爪蟾卵中纯化了一种新的异二聚因子,称为DNA解链因子(DUF),它由87 kDa和140 kDa多肽组成。在拓扑异构酶I存在的情况下,DUF可以解开封闭的圆形双链DNA,但是它不具有DNA旋转酶活性:它不会以ATP水解为代价将负超螺旋引入DNA。编码这两种多肽的cDNA的克隆和测序表明,该87 kDa多肽与哺乳动物HMG蛋白T160 /结构特异性识别蛋白同源。 140 kDa多肽与酵母Cdc68同源,后者是一种通过调节染色质结构来控制细胞周期G1期几个基因表达的蛋白质。非洲爪蟾卵提取物中对DUF的免疫缺陷化大大降低了提取物复制外源添加的精子染色质或质粒DNA的能力。结论:我们建议DUF在非洲爪蟾卵提取物中的DNA复制中起作用。

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