Regulation of expression of late genes of bacteriophage T5

Journal of Virology
|January 1, 1974
PubMed

Insights

Bacteriophage T5 gene C2 mutants prevent late protein synthesis by blocking RNA transcription. This gene product is crucial for both early and late viral gene expression during infection.

Area of Science:

  • Molecular Biology
  • Virology
  • Genetics

Background:

  • Bacteriophage T5 employs intricate regulatory mechanisms for gene expression during infection.
  • Understanding phage gene regulation is key to controlling viral replication and developing antiviral strategies.

Purpose of the Study:

  • To characterize amber mutants of bacteriophage T5 defective in gene C2.
  • To elucidate the role of the gene C2 product in viral gene expression, particularly during late stages of infection.

Main Methods:

  • Characterization of bacteriophage T5 amber mutants.
  • Analysis of RNA and protein synthesis in infected nonpermissive cells.
  • Assessment of cellular factors like lysis, energy supply, and DNA integrity.

Main Results:

  • Mutants defective in gene C2 are unable to initiate normal synthesis of late RNAs and proteins.
  • The gene C2 product is also required for sustained early RNA and protein synthesis during late infection stages.
  • Inability to synthesize proteins is not caused by premature lysis, energy depletion, or DNA degradation.

Conclusions:

  • The product of bacteriophage T5 gene C2 plays a critical role in regulating both early and late viral transcription.
  • Gene C2 is essential for the coordinated expression of the viral genome throughout the infection cycle.

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