Brendler T, Abeles A, Austin S
Laboratory of Chromosome Biology, ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, MD 21702-1201, USA.
EMBO J. 1995 Aug 15;14(16):4083-9. doi: 10.1002/j.1460-2075.1995.tb00080.x.
The P1 plasmid replication origin P1oriR is controlled by methylation of four GATC adenine methylation sites within heptamer repeats. A comparable (13mer) region is present in the host origin, oriC. The two origins show comparable responses to methylation; negative control by recognition of hemimethylated DNA (sequestration) and a positive requirement for methylation for efficient function. We have isolated a host protein that recognizes the P1 origin region only when it is isolated from a strain proficient for adenine methylation. The substantially purified 22 kDa protein also binds to the 13mer region of oriC in a methylation-specific fashion. It proved to be the product of the seqA gene that acts in the negative control of oriC by sequestration. We conclude that the role of the SeqA protein in sequestration is to recognize the methylation state of P1oriR and oriC by direct DNA binding. Using synthetic substrates we show that SeqA binds exclusively to the hemimethylated forms of these origins forms that are the immediate products of replication in a methylation-proficient strain. We also show that the protein can recognize sequences with multiple GATC sites, irrespective of the surrounding sequence. The basis for origin specificity is primarily the persistence of hemimethylated forms that are over-represented in the natural. DNA preparations relative to controls.
P1 质粒复制起点 P1oriR 受七聚体重复序列内四个 GATC 腺嘌呤甲基化位点的甲基化作用控制。宿主复制起点 oriC 中存在一个类似的(13 聚体)区域。这两个复制起点对甲基化表现出相似的反应:通过识别半甲基化 DNA(隔离)进行负调控,以及甲基化对高效功能的正需求。我们分离出了一种宿主蛋白,该蛋白仅在从腺嘌呤甲基化 proficient 的菌株中分离出 P1 复制起点区域时才会识别它。这种经过大量纯化的 22 kDa 蛋白也以甲基化特异性方式与 oriC 的 13 聚体区域结合。事实证明它是 seqA 基因的产物,通过隔离作用对 oriC 进行负调控。我们得出结论,SeqA 蛋白在隔离中的作用是通过直接结合 DNA 来识别 P1oriR 和 oriC 的甲基化状态。使用合成底物,我们表明 SeqA 仅与这些复制起点的半甲基化形式结合,这些形式是甲基化 proficient 菌株中复制的直接产物。我们还表明,该蛋白可以识别具有多个 GATC 位点的序列,而与周围序列无关。复制起点特异性的基础主要是半甲基化形式的持久性,在天然 DNA 制剂中相对于对照,其含量过高。