Wichitwechkarn J, Bailey S, Bodley J W, Anderson D
Department of Microbiology/Dentistry, University of Minnesota, Minneapolis 55455.
Nucleic Acids Res. 1989 May 11;17(9):3459-68. doi: 10.1093/nar/17.9.3459.
We previously demonstrated (Guo et al., 1987. Nucl. Acids Res. 15, 7081-7090) that purified proheads of bacteriophage phi 29 contain an RNA of 120 bases which is essential for DNA packaging. Here we report that this RNA exists primarily as a polymer of ca. 174 residues in phage-infected cells and that ca. 54 bases are cleaved from its 3'-terminus by adventitious nucleases during the purification of proheads. The long and short forms of the RNA had similar activity in in vitro DNA packaging and phage assembly. We report the sequence of the long form of the RNA and show that similar long and short forms can be isolated from the proheads of the phi 29 relatives phi 21, phi 15 and SF5. The concentration dependence in the reconstitution of RNA-free proheads suggests that one copy of the RNA is sufficient to restore DNA packaging activity to RNA-free proheads. However, quantitative measurements indicate that 5 to 6 copies of the RNA are present on proheads isolated from phage-infected cells.
我们先前已证明(Guo等人,1987年。《核酸研究》15卷,7081 - 7090页),噬菌体phi 29的纯化原头部含有一段120个碱基的RNA,它对DNA包装至关重要。在此我们报告,这种RNA在噬菌体感染的细胞中主要以约174个残基的聚合物形式存在,并且在原头部纯化过程中,其3'末端约54个碱基会被偶然的核酸酶切割。RNA的长形式和短形式在体外DNA包装和噬菌体组装中具有相似的活性。我们报告了RNA长形式的序列,并表明可以从phi 29的亲缘噬菌体phi 21、phi 15和SF5的原头部中分离出相似的长形式和短形式。无RNA原头部重构中的浓度依赖性表明,一份RNA就足以将DNA包装活性恢复到无RNA的原头部。然而,定量测量表明,从噬菌体感染细胞中分离出的原头部上存在5到6份这种RNA。