Zhang F, Anderson D
Department of Genetics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J Biol Chem. 1998 Jan 30;273(5):2947-53. doi: 10.1074/jbc.273.5.2947.
Prohead RNA (pRNA) of the Bacillus subtilis bacteriophage phi29 is needed for in vitro packaging of DNA-gene product 3 (DNA-gp3). Residues 22-84 of the 174-base pRNA bind the portal vertex of the prohead, the site of DNA packaging. To define the nucleotides of pRNA needed for prohead binding and DNA-gp3 packaging and to seek biologically active variants of pRNA, segments of pRNA were randomized to obtain vast repertoires of RNA molecules. RNA aptamers, ligands best suited for prohead binding, were obtained by multiple rounds of in vitro selection. Evolution of pRNA aptamers was followed by a competition binding assay and nucleotide sequencing, and mutants were tested for DNA-gp3 packaging. Aptamers selected following randomization of the E stem and loop and a part of the C-E loop that were active in DNA-gp3 packaging were invariably wild-type. DNA-gp3 packaging activity also required nucleotides G82 and G83 that form base pairs intermolecularly with C47 and C48 to produce a novel hexameric oligomer of pRNA. The only mutant aptamers that retained full DNA-gp3 packaging activity showed changes of the U residues at positions 81, 84, and 85 of the D loop. Thus, the in vitro selections essentially recapitulated the natural evolution of pRNA.
枯草芽孢杆菌噬菌体phi29的前头部RNA(pRNA)是DNA基因产物3(DNA-gp3)体外包装所必需的。174个碱基的pRNA的22-84位残基与前头部的门户顶点结合,即DNA包装的位点。为了确定前头部结合和DNA-gp3包装所需的pRNA核苷酸,并寻找pRNA的生物活性变体,对pRNA片段进行随机化处理以获得大量的RNA分子库。通过多轮体外筛选获得了最适合前头部结合的RNA适配体(配体)。通过竞争结合试验和核苷酸测序跟踪pRNA适配体的进化,并对突变体进行DNA-gp3包装测试。在E茎环和部分C-E环随机化后选择的、在DNA-gp3包装中具有活性的适配体总是野生型的。DNA-gp3包装活性还需要核苷酸G82和G83,它们与C47和C48分子间形成碱基对,从而产生一种新型的pRNA六聚体寡聚物。唯一保留完全DNA-gp3包装活性的突变体适配体显示D环81、84和85位的U残基发生了变化。因此,体外筛选基本上重现了pRNA的自然进化。