Qimron Udi, Kulczyk Arkadiusz W, Hamdan Samir M, Tabor Stanley, Richardson Charles C
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.
Mol Microbiol. 2008 Jan;67(2):448-57. doi: 10.1111/j.1365-2958.2007.06058.x. Epub 2007 Dec 5.
Overexpression of udk, an Escherichia coli gene encoding a uridine/cytidine kinase, interferes with T7 bacteriophage growth. We show here that inhibition of T7 phage growth by udk overexpression can be overcome by inhibition of host RNA polymerase. Overexpression of gene 2, whose product inhibits host RNA polymerase, restores T7 phage growth on hosts overexpressing udk. In addition, rifampicin, an inhibitor of host RNA polymerase, restores the burst size of T7 phage on udk-overexpressing hosts to normal. In agreement with these findings, suppressor mutants that overcome the inhibition arising from udk overexpression gain the ability to grow on hosts that are resistant to inhibition of RNA polymerase by gene 2 protein, and suppressor mutants that overcome a lack of gene 2 protein gain the ability to grow on hosts that overexpress udk. Mutations that eliminate or weaken strong promoters for host RNA polymerase in T7 DNA, and mutations in T7 gene 3.5 that affect its interaction with T7 RNA polymerase, also reduce the interference with T7 growth by host RNA polymerase. We propose a general model for the requirement of host RNA polymerase inhibition.
大肠杆菌中编码尿苷/胞苷激酶的udk基因的过表达会干扰T7噬菌体的生长。我们在此表明,udk过表达对T7噬菌体生长的抑制作用可通过抑制宿主RNA聚合酶来克服。基因2的过表达,其产物可抑制宿主RNA聚合酶,能恢复T7噬菌体在过表达udk的宿主上的生长。此外,利福平,一种宿主RNA聚合酶抑制剂,可将T7噬菌体在过表达udk的宿主上的爆发量恢复至正常。与这些发现一致,克服udk过表达所产生抑制作用的抑制突变体获得了在对基因2蛋白抑制RNA聚合酶有抗性的宿主上生长的能力,而克服基因2蛋白缺失的抑制突变体获得了在过表达udk的宿主上生长的能力。消除或削弱T7 DNA中宿主RNA聚合酶强启动子的突变,以及影响T7基因3.5与T7 RNA聚合酶相互作用的突变,也会减少宿主RNA聚合酶对T7生长的干扰。我们提出了一个关于宿主RNA聚合酶抑制需求的通用模型。