Alcorlo Martín, González-Huici Víctor, Hermoso José M, Meijer Wilfried J J, Salas Margarita
Instituto de Biología Molecular Eladio Viñuela, Centro de Biología Molecular Severo Ochoa, Universidad Autónoma, Canto Blanco, 28049 Madrid, Spain.
J Bacteriol. 2007 Aug;189(15):5542-9. doi: 10.1128/JB.00402-07. Epub 2007 May 25.
It is becoming clear that in vivo phage DNA ejection is not a mere passive process. In most cases, both phage and host proteins seem to be involved in pulling at least part of the viral DNA inside the cell. The DNA ejection mechanism of Bacillus subtilis bacteriophage phi29 is a two-step process where the linear DNA penetrates the cell with a right-left polarity. In the first step approximately 65% of the DNA is pushed into the cell. In the second step, the remaining DNA is actively pulled into the cytoplasm. This step requires protein p17, which is encoded by the right-side early operon that is ejected during the first push step. The membrane protein p16.7, also encoded by the right-side early operon, is known to play an important role in membrane-associated phage DNA replication. In this work we show that, in addition, p16.7 is required for efficient execution of the second pull step of DNA ejection.
越来越明显的是,体内噬菌体DNA的注入并非仅仅是一个被动过程。在大多数情况下,噬菌体和宿主蛋白似乎都参与了将至少部分病毒DNA拉进细胞内的过程。枯草芽孢杆菌噬菌体phi29的DNA注入机制是一个两步过程,其中线性DNA以从右到左的极性穿透细胞。在第一步中,大约65%的DNA被推进细胞。在第二步中,剩余的DNA被主动拉进细胞质。这一步需要蛋白质p17,它由右侧早期操纵子编码,在第一步推进过程中被注入。膜蛋白p16.7也由右侧早期操纵子编码,已知在与膜相关的噬菌体DNA复制中起重要作用。在这项工作中我们表明,此外,p16.7对于高效执行DNA注入的第二步拉动过程也是必需的。