HOST-VIRUS INTERACTIONS IN THE CONTROL OF T4-PREREPLICATIVE TRANSCRIPTION .1. TABC (RHO) MUTANTS

In this paper we describe properties of old (Takahashi, 1978) and new tabCts and tabCcs bacterial mutants. We find that under non-permissive conditions they differently inhibit the synthesis of specific T4 prereplicative gene products. Among such products, that we have been able to identify, are P43 and PrIIA. In contrast, P32 and PrIIB are not affected. Inhibition of P43 (T4 DNA polymerase) synthesis is sufficient to account for depressed DNA synthesis in tabC (Takahashi, 1978). In heterodiploids: (1) all tabC mutants are recessive; (2) all tabC mutants do not complement with each other; (3) at least one, tabCts-5521, becomes dominant at 42.6 °C if rho mutant ts15 (Tab+) (Das et al., 1976) is situated in trans; (4) tabCts-5521 also becomes dominant at 42.6 °C if tabCcs-110 and tabCcs-18 are situated in trans (42.6 °C is non-permissive for T4 development on tabCcs-5521 and permissive for T4 development on tabCcs mutants). We discuss the possibility that in tabC mutants rho protein is altered and insensitive to T4-specific anti-termination functions. We also discuss a model that accounts for the differential effect of tabC mutants on the synthesis of T4 prereplicative proteins. © 1979.