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Updated: Aug 19, 2026

The MultiBac Protein Complex Production Platform at the EMBL
Published on: July 11, 2013
Characterization of Plys-proximal morphogenetic genes of transposable bacteriophage Mu
1Department of Microbiology and Immunology, McGill University, Montreal, Canada. irsiboo@itsa.ucsf.edu
Abstract:
Late during the bacteriophage Mu lytic cycle, Mu DNA must be matured and packaged from its dispersed integration sites in the host DNA in order to produce progeny virions. Whereas control of late gene transcription in Mu is becoming well understood, less is known about the phage morphogenetic process. To investigate the latter, we cloned and sequenced a approximately 4.3-kb region of the phage DNA beginning just upstream of the leftmost late promoter Plys. Previous mapping of amber mutations had located the lysis (lys) and proposed DNA maturation genes D and E in this region. When the DNA sequence was analyzed, seven potential open reading frames were found. DNA sequence analysis of amber mutations in genes D and E identified the sixth and seventh open reading frames as D and E, respectively. Cloning and expression of this region enabled production of cell-free protein extracts that specifically recognize the phage-encoded packaging sequence (pac), a characteristic exhibited by phage maturation enzymes. In addition, the E protein was found to share homology with the large subunit of many phage DNA maturation enzymes. These results support the hypothesis that D and E encode subunits of the Mu DNA maturation enzyme.
Insights
Bacteriophage Mu DNA maturation and packaging are crucial for producing new viruses. This study identifies genes D and E as key components of the Mu DNA maturation enzyme, essential for phage assembly.
Area of Science:
- Molecular Biology
- Virology
- Bacteriophage Genetics
Background:
- The bacteriophage Mu lytic cycle requires DNA maturation and packaging for progeny virion production.
- While late gene transcription in bacteriophage Mu is understood, the phage morphogenetic process remains less clear.
Purpose of the Study:
- To investigate the phage morphogenetic process by analyzing a specific DNA region.
- To identify and characterize genes involved in bacteriophage Mu DNA maturation and packaging.
Main Methods:
- Cloning and sequencing of a 4.3-kb bacteriophage Mu DNA region.
- DNA sequence analysis of amber mutations in genes D and E.
- Cloning and expression of the DNA region to produce cell-free protein extracts.
Main Results:
- Seven potential open reading frames were identified in the sequenced region.
- Genes D and E were identified as the sixth and seventh open reading frames, respectively.
- Cell-free extracts recognized the phage packaging sequence (pac); E protein showed homology to known DNA maturation enzymes.
Conclusions:
- Genes D and E encode subunits of the bacteriophage Mu DNA maturation enzyme.
- This finding contributes to understanding bacteriophage Mu morphogenesis and DNA packaging.
Related Concept Videos
Lytic Cycle of Bacteriophages
Lysogenic Cycle of Bacteriophages
Transposons
Viral Replication: Lysogenic Cycle
DNA Bacteriophages
Bacteriophages of the Human Virome

