Reid R J, Bodley J W, Anderson D
Department of Genetics and Cell Biology, University of Minnesota, Minneapolis 55455.
J Biol Chem. 1994 Feb 18;269(7):5157-62.
The small prohead RNA (pRNA) of the Bacillus subtilis bacteriophage phi 29 is essential for ATP-dependent packaging of viral DNA. The 174-, 124-, and 120-residue forms of pRNA produced in vitro using T7 RNA polymerase were equivalent in prohead binding and DNA packaging activity to pRNAs produced in phi 29-infected cells. pRNA binding to proheads, characterized by the use of Northern hybridization and filter binding assays, was specific, rapid, and irreversible in the presence of 10 mM Mg2+. Proheads produced in phage-infected cells carried 5.8 +/- 2.7 copies of pRNA, and proheads assembled in Escherichia coli in the absence of pRNA bound 6.0 +/- 3.5 copies of pRNA. Footprints of proheads on pRNA generated with the ribonucleases A, T1, and V1 showed that nucleotides 22-84, 5' to 3', were protected from ribonuclease attack. Enhanced cleavage at nucleotides 37-40 with ribonuclease V1 suggested a conformational change of pRNA upon prohead binding.
枯草芽孢杆菌噬菌体phi 29的小前头部RNA(pRNA)对于病毒DNA的ATP依赖性包装至关重要。使用T7 RNA聚合酶在体外产生的174、124和120个残基形式的pRNA,在与前头部结合和DNA包装活性方面,与在phi 29感染细胞中产生的pRNA相当。通过Northern杂交和滤膜结合试验表征,pRNA与前头部的结合在10 mM Mg2+存在下具有特异性、快速且不可逆。在噬菌体感染细胞中产生的前头部携带5.8 +/- 2.7个pRNA拷贝,而在没有pRNA的情况下在大肠杆菌中组装的前头部结合6.0 +/- 3.5个pRNA拷贝。用核糖核酸酶A、T1和V1对前头部在pRNA上产生的足迹表明,5'至3'方向的核苷酸22 - 84免受核糖核酸酶攻击。核糖核酸酶V1在核苷酸37 - 40处增强的切割表明,pRNA在前头部结合时发生了构象变化。