García J A, Peñalva M A, Blanco L, Salas M
Proc Natl Acad Sci U S A. 1984 Jan;81(1):80-4. doi: 10.1073/pnas.81.1.80.
The template requirements for the formation of the phi 29 protein p3-dAMP initiation complex in vitro have been studied. The initiation reaction requires the parental protein p3 but not an intact DNA molecule. Protein p3-containing fragments from the left- or right-hand DNA ends were active as template for formation of the initiation complex provided they had a minimal size: a 26-base-pair-long fragment was active whereas a 10-base-pair-long one was essentially inactive. However, the activity of the latter was restored by ligation of an unspecific DNA sequence. phi 29 DNA internal fragments, as well as denatured phi 29 DNA, were inactive as template for the initiation reaction. The terminal protein-DNA complex isolated from Bacillus phage phi 15 was active in formation of the phi 29 p3-dAMP complex, whereas the protein-DNA complex isolated from Bacillus phage GA-1 or from the pneumococcal phage Cp-1, both with a morphology similar to that of phage phi 29, as well as that obtained from adenovirus, were inactive.
已对体外形成φ29蛋白p3-dAMP起始复合物的模板要求进行了研究。起始反应需要亲本蛋白p3,但不需要完整的DNA分子。来自左手或右手DNA末端的含蛋白p3片段只要具有最小尺寸,作为起始复合物形成的模板就是有活性的:一个26个碱基对长的片段是有活性的,而一个10个碱基对长的片段基本上是无活性的。然而,通过连接非特异性DNA序列可恢复后者的活性。φ29 DNA内部片段以及变性的φ29 DNA作为起始反应的模板是无活性的。从芽孢杆菌噬菌体φ15分离的末端蛋白-DNA复合物在形成φ29 p3-dAMP复合物方面是有活性的,而从芽孢杆菌噬菌体GA-1或肺炎球菌噬菌体Cp-1分离的蛋白-DNA复合物(两者形态均与噬菌体φ29相似)以及从腺病毒获得的蛋白-DNA复合物是无活性的。