scholarly journals PARTIAL EXCLUSION BETWEEN T-EVEN BACTERIOPHAGES; AN INCIPIENT GENETIC ISOLATION MECHANISM

Genetics ◽  
1974 ◽  
Vol 78 (4) ◽  
pp. 989-1014
Author(s):  
Richard L Russell ◽  
Robert J Huskey

ABSTRACT Conditional lethal mutant systems developed in T-even bacteriophages T2, T4 and T6 have been used to study the partial exclusion which characterizes mixed infections of these phages. In bacteria mixedly infected with T2 and T4, the dominant phage (T4) acts against localized exclusion sensitivity determinants in the genome of the excluded phage (T2). These determinants are clustered near genes controlling early functions; the determinants themselves do not appear among the progeny, but markers located close to them appear infrequently, by recombination. The excluding action of T4 does not depend on the action of any gene so far identified by conditional lethal mutations, nor does it depend on differences in DNA glucosylation between infecting phages. Regardless of mechanism, the genetic consequence of this partial exclusion is to limit genetic exchange between T2 and T4 in the region of the genome controlling early functions, while retaining the capacity for extensive exchange in other regions; in short, partial exclusion constitutes a localized genetic isolating mechanism. Related forms of partial exclusion characterize mixed infections of other T-even phages, including those of some phages newly isolated from nature.

Virology ◽  
1984 ◽  
Vol 132 (2) ◽  
pp. 436-444 ◽  
Author(s):  
Beatriz G.T. Pogo ◽  
Elchonon M. Berkowitz ◽  
Samuel Dalest

2006 ◽  
Vol 188 (5) ◽  
pp. 1969-1978 ◽  
Author(s):  
Lydia Dubytska ◽  
Henry P. Godfrey ◽  
Felipe C. Cabello

ABSTRACT ftsZ is essential for cell division in many microorganisms. In Escherichia coli and Bacillus subtilis, FtsZ plays a role in ring formation at the leading edge of the cell division septum. An ftsZ homologue is present in the Borrelia burgdorferi genome (ftsZBbu ). Its gene product (FtsZBbu) is strongly homologous to other bacterial FtsZ proteins, but its function has not been established. Because loss-of-function mutants of ftsZBbu might be lethal, the tetR/tetO system was adapted for regulated control of this gene in B. burgdorferi. Sixty-two nucleotides of an ftsZBbu antisense DNA sequence under the control of a tetracycline-responsive modified hybrid borrelial promoter were cloned into pKFSS1. This construct was electroporated into a B. burgdorferi host strain carrying a chromosomally located tetR under the control of the B. burgdorferi flaB promoter. After induction by anhydrotetracycline, expression of antisense ftsZ RNA resulted in generation of filamentous B. burgdorferi that were unable to divide and grew more slowly than uninduced cells. To determine whether FtsZBbu could interfere with the function of E. coli FtsZ, ftsZBbu was amplified from chromosomal DNA and placed under the control of the tetracycline-regulated hybrid promoter. After introduction of the construct into E. coli and induction with anhydrotetracycline, overexpression of ftsZBbu generated a filamentous phenotype. This suggested interference of ftsZBbu with E. coli FtsZ function and confirmed the role of ftsZBbu in cell division. This is the first report of the generation of a B. burgdorferi conditional lethal mutant equivalent by tetracycline-controlled expression of antisense RNA.


1996 ◽  
Vol 271 (10) ◽  
pp. 5704-5711 ◽  
Author(s):  
Colin Gordon ◽  
Gordon McGurk ◽  
Mairi Wallace ◽  
Nicholas D. Hastie

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