Hoffman B, Levine M
J Virol. 1975 Dec;16(6):1547-59. doi: 10.1128/JVI.16.6.1547-1559.1975.
P16 is a virion protein and, as such, is incorporated into the phage head as a step in morphogenesis. The role of P16 in assembly is not essential since particles are formed without this protein which appear normal by electron microscopy. P16 is essential when the particle infects a cell in the following cycle of infection. In the absence of functional P16, the infection does not appear to proceed beyond release of phage DNA from the capsid. No known genes are expressed, no DNA is transcribed, and the host cell survives the infection, continuing to grow and divide normally. The P16 function is required only during infection for the expression of phage functions. Induction in the absence of P16 proceeds with the expression of early and late genes and results in particle formation. P16 must be incorporated during morphogenesis into progeny particles after both infection and induction for the progeny to be infectious. The P16 function is necessary for transduction as well as for infection. Its activity is independent of new protein synthesis and it is not under immunity control. P16 can act in trans, but appears to act preferentially on the phage or phage DNA with which it is packaged. The data from complementation studies are compatible with P16 release from the capsid with the phage DNA. In the absence of P16 the infection is blocked, but the phage genome is not degraded. The various roles which have been ruled out for P16 are: (i) an early regulatory function, (ii) an enzymatic activity necessary for phage production, (iii) protection of phage DNA from host degradation enzymes, (iv) any generalized alteration of the host cell, (v) binding parental DNA to the replication complex, and (vi) any direct involvement in the replication of P22 DNA. P16 can be responsible for: (i) complete release of the DNA and disengagement from the capsid, (ii) bringing the released DNA to some necessary cell site or compartment such as the cytoplasm, (iii) removal of other virion proteins from the injected DNA, and (iv) alterations of the structure of the injected DNA.
P16是一种病毒粒子蛋白,因此,作为形态发生过程中的一个步骤,它被整合到噬菌体头部。P16在组装过程中的作用并非必不可少,因为在没有这种蛋白质的情况下也能形成粒子,通过电子显微镜观察,这些粒子看起来是正常的。当粒子在下一轮感染中感染细胞时,P16是必不可少的。在没有功能性P16的情况下,感染似乎不会在噬菌体DNA从衣壳释放后继续进行。没有已知基因表达,没有DNA转录,宿主细胞在感染中存活下来,继续正常生长和分裂。P16功能仅在感染期间是噬菌体功能表达所必需的。在没有P16的情况下诱导会伴随着早期和晚期基因的表达,并导致粒子形成。为了使子代具有感染性,P16必须在形态发生过程中在感染和诱导后被整合到子代粒子中。P16功能对于转导以及感染都是必需的。其活性独立于新的蛋白质合成,且不受免疫控制。P16可以反式作用,但似乎优先作用于与其包装在一起的噬菌体或噬菌体DNA。互补研究的数据与P16随噬菌体DNA从衣壳释放相符。在没有P16的情况下,感染被阻断,但噬菌体基因组不会降解。已被排除的P16的各种作用包括:(i)早期调节功能;(ii)噬菌体产生所需的酶活性;(iii)保护噬菌体DNA免受宿主降解酶的作用;(iv)宿主细胞的任何普遍改变;(v)将亲本DNA与复制复合体结合;(vi)任何直接参与P22 DNA复制的作用。P16可能负责:(i)DNA的完全释放以及与衣壳的脱离;(ii)将释放的DNA带到某些必要的细胞位点或区室,如细胞质;(iii)从注入的DNA中去除其他病毒粒子蛋白;(iv)改变注入DNA的结构。