首页> 美国卫生研究院文献>other >The Escherichia coli Cryptic Prophage Protein YfdR Binds to DnaA and Initiation of Chromosomal Replication Is Inhibited by Overexpression of the Gene Cluster yfdQ-yfdR-yfdS-yfdT
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The Escherichia coli Cryptic Prophage Protein YfdR Binds to DnaA and Initiation of Chromosomal Replication Is Inhibited by Overexpression of the Gene Cluster yfdQ-yfdR-yfdS-yfdT

机译:大肠杆菌隐性噬菌体蛋白YfdR绑定到DnaA和染色体复制的启动被基因簇yfdQ-yfdR-yfdS-yfdT的过表达抑制

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摘要

The initiation of bacterial chromosomal replication is regulated by multiple pathways. To explore novel regulators, we isolated multicopy suppressors for the cold-sensitive hda-185 ΔsfiA(sulA) mutant. Hda is crucial for the negative regulation of the initiator DnaA and the hda-185 mutation causes severe replication overinitiation at the replication origin oriC. The SOS-associated division inhibitor SfiA inhibits FtsZ ring formation, an essential step for cell division regulation during the SOS response, and ΔsfiA enhances the cold sensitivity of hda-185 cells in colony formation. One of the suppressors comprised the yfdQ-yfdR-yfdS-yfdT gene cluster carried on a cryptic prophage. Increased copy numbers of yfdQRT or yfdQRS inhibited not only hda-185-dependent overinitiation, but also replication overinitiation in a hyperactive dnaA mutant, and in a mutant lacking an oriC-binding initiation-inhibitor SeqA. In addition, increasing the copy number of the gene set inhibited the growth of cells bearing specific, initiation-impairing dnaA mutations. In wild-type cells, multicopy supply of yfdQRT or yfdQRS also inhibited replication initiation and increased hydroxyurea (HU)-resistance, as seen in cells lacking DiaA, a stimulator of DnaA assembly on oriC. Deletion of the yfdQ-yfdR-yfdS-yfdT genes did not affect either HU resistance or initiation regulation. Furthermore, we found that DnaA bound specifically to YfdR in soluble protein extracts oversupplied with YfdQRST. Purified YfdR also bound to DnaA, and DnaA Phe46, an amino acid residue crucial for DnaA interactions with DiaA and DnaB replicative helicase was important for this interaction. Consistently, YfdR moderately inhibited DiaA-DnaA and DnaB-DnaA interactions. In addition, protein extracts oversupplied with YfdQRST inhibited replication initiation in vitro. Given the roles of yfdQ and yfdS in cell tolerance to specific environmental stresses, the yfdQ-yfdR-yfdS-yfdT genes might downregulate the initiator DnaA-oriC complex under specific growth conditions.
机译:细菌染色体复制的启动受多种途径调控。为了探索新型调节剂,我们分离了冷敏hda-185ΔsfiA(sulA)突变体的多拷贝抑制子。 Hda对于启动子DnaA的负调控至关重要,hda-185突变会导致复制起点oriC处严重的复制过度初始化。与SOS相关的分裂抑制剂SfiA抑制FtsZ环的形成,这是SOS应答过程中细胞分裂调节的重要步骤,而ΔsfiA增强了hda-185细胞对菌落形成的冷敏感性。抑制子之一包括携带隐性噬菌体的yfdQ-yfdR-yfdS-yfdT基因簇。 yfdQRT或yfdQRS拷贝数的增加不仅抑制了hda-185依赖的过度启动,而且抑制了过度活跃的dnaA突变体和缺少oriC结合启动抑制剂SeqA的突变体中的复制过度启动。此外,增加基因组的拷贝数会抑制带有特定的,起始受损dnaA突变的细胞的生长。在野生型细胞中, yfdQRT yfdQRS 的多拷贝供应也抑制复制起始并增加对羟基脲(HU)的抵抗力,这在缺乏DiaA(DnaA刺激物)的细胞中可见。在 oriC 上进行汇编。删除 yfdQ - yfdR - yfdS - yfdT 基因既不影响HU抗性,也不影响启动调控。此外,我们发现DnaA与YfdQRST过量供应的可溶性蛋白提取物中的YfdR特异性结合。纯化的YfdR也与DnaA和DnaA Phe46结合,DnaA与DiaA和DnaB复制解旋酶相互作用至关重要的氨基酸残基对于这种相互作用很重要。一致地,YfdR适度抑制DiaA-DnaA和DnaB-DnaA相互作用。此外,过量供应YfdQRST的蛋白质提取物会抑制体外复制启动。。考虑到 yfdQ yfdS 在细胞对特定环境胁迫的耐受性中的作用, yfdQ - yfdR - yfdS - yfdT 基因可能下调启动子DnaA- oriC 复合物。

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