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调控乳酸克鲁维酵母中KARS12染色体复制起点的DNA元件。

DNA elements modulating the KARS12 chromosomal replicator in Kluyveromyces lactis.

作者信息

Irene Carmela, Maciariello Clelia, Micheli Gioacchino, Theis James F, Newlon Carol S, Fabiani Lucia

机构信息

Dipartimento di Biologia Cellulare e dello Sviluppo, Università La Sapienza, Piazzale A. Moro, 5, Roma, Italy.

出版信息

Mol Genet Genomics. 2007 Mar;277(3):287-99. doi: 10.1007/s00438-006-0188-7. Epub 2006 Nov 29.

Abstract

Eukaryotic chromosomal DNA replication is initiated by a highly conserved set of proteins that interact with cis-acting elements on chromosomes called replicators. Despite the conservation of replication initiation proteins, replicator sequences show little similarity from species to species in the small number of organisms that have been examined. Examination of replicators in other species is likely to reveal common features of replicators. We have examined a Kluyeromyces lactis replicator, KARS12, that functions as origin of DNA replication on plasmids and in the chromosome. It contains a 50-bp region with similarity to two other K. lactis replicators, KARS101 and the pKD1 replication origin. Replacement of the 50-bp sequence with an EcoRI site completely abrogated the ability of KARS12 to support plasmid and chromosomal DNA replication origin activity, demonstrating this sequence is a common feature of K. lactis replicators and is essential for function, possibly as the initiator protein binding site. Additional sequences up to 1 kb in length are required for efficient KARS12 function. Within these sequences are a binding site for a global regulator, Abf1p, and a region of bent DNA, both of which contribute to the activity of KARS12. These elements may facilitate protein binding, protein/protein interaction and/or nucleosome positioning as has been proposed for other eukaryotic origins of DNA replication.

摘要

真核染色体DNA复制由一组高度保守的蛋白质启动,这些蛋白质与染色体上称为复制子的顺式作用元件相互作用。尽管复制起始蛋白具有保守性,但在已研究的少数生物体中,复制子序列在物种间几乎没有相似性。对其他物种复制子的研究可能会揭示复制子的共同特征。我们研究了乳酸克鲁维酵母复制子KARS12,它在质粒和染色体上作为DNA复制起点发挥作用。它包含一个50bp的区域,与另外两个乳酸克鲁维酵母复制子KARS101和pKD1复制起点相似。用EcoRI位点取代50bp序列完全消除了KARS12支持质粒和染色体DNA复制起点活性的能力,表明该序列是乳酸克鲁维酵母复制子的共同特征,并且对于功能是必不可少的,可能作为起始蛋白结合位点。高效的KARS12功能还需要长达1kb的其他序列。在这些序列中有一个全局调节因子Abf1p的结合位点和一个DNA弯曲区域,这两者都对KARS12的活性有贡献。正如针对其他真核生物DNA复制起点所提出的那样,这些元件可能促进蛋白质结合、蛋白质/蛋白质相互作用和/或核小体定位。

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