Mosig G, Bock S
J Virol. 1976 Mar;17(3):756-61. doi: 10.1128/JVI.17.3.756-761.1976.
Genes 46 and 47 of phage T4 control a nuclease that is required for genetic recombination and may act similarly to the Escherichia coli RecBC nuclease. In vivo, the nucleolytic activities of both of these nucleases must be moderated so that recombining DNA intermediates are not destroyed. We conclude from our present experiments that the phage T4 gene 32 protein, specifically its C-terminal domain, participates in such moderation. We have investigated DNA degradation in different gene 32 and gene 32/46 mutants under conditions that are completely restrictive for progeny production in all the mutants. Under these conditions, DNA of those gene 32 mutants in which the C-terminal domain of the protein is not synthesized or is modified is degraded to acid-soluble material. T4 gene 46 or E. coli recB mutations reduce such degradation; together they abolish it completely. By contrast, single gene 32 mutants which produce an unaltered C-terminal domain show little or no degradation of their DNA. Residual protection against nucleases is unrelated to residual primary DNA replication or to overproduction of the mutant peptides in the different gene 32 mutants.
噬菌体T4的基因46和47控制着一种核酸酶,这种核酸酶是基因重组所必需的,其作用可能类似于大肠杆菌的RecBC核酸酶。在体内,必须调节这两种核酸酶的核酸水解活性,以使重组DNA中间体不被破坏。我们从目前的实验中得出结论,噬菌体T4基因32蛋白,特别是其C末端结构域,参与了这种调节。我们研究了在对所有突变体的子代产生完全限制的条件下,不同基因32和基因32/46突变体中的DNA降解情况。在这些条件下,那些蛋白质C末端结构域未合成或被修饰的基因32突变体的DNA被降解为酸溶性物质。T4基因46或大肠杆菌recB突变会减少这种降解;它们共同作用则会完全消除这种降解。相比之下,产生未改变的C末端结构域的单基因32突变体的DNA几乎没有或没有降解。对核酸酶的残余保护与残余的初级DNA复制或不同基因32突变体中突变肽的过量产生无关。