Related Experiment Video
Updated: Jul 14, 2026

Visualization and Quantitative Analysis of Genotoxin-Induced PARP1/PARP2 Activation in Cells Using a Fluorescent Fusion Protein-Based Reporter
Published on: April 17, 2026
The phage phi29 membrane protein p16.7, involved in DNA replication, is required for efficient ejection of the viral
Martín Alcorlo1, Víctor González-Huici, José M Hermoso
1Instituto de Biología Molecular Eladio Viñuela, Centro de Biología Molecular Severo Ochoa, Universidad Autónoma, Canto Blanco, 28049 Madrid, Spain.
Abstract:
It is becoming clear that in vivo phage DNA ejection is not a mere passive process. In most cases, both phage and host proteins seem to be involved in pulling at least part of the viral DNA inside the cell. The DNA ejection mechanism of Bacillus subtilis bacteriophage phi29 is a two-step process where the linear DNA penetrates the cell with a right-left polarity. In the first step approximately 65% of the DNA is pushed into the cell. In the second step, the remaining DNA is actively pulled into the cytoplasm. This step requires protein p17, which is encoded by the right-side early operon that is ejected during the first push step. The membrane protein p16.7, also encoded by the right-side early operon, is known to play an important role in membrane-associated phage DNA replication. In this work we show that, in addition, p16.7 is required for efficient execution of the second pull step of DNA ejection.
Insights
Bacteriophage phi29 DNA ejection involves active protein participation. Protein p16.7 is essential for the second, pulling step of viral DNA entry into Bacillus subtilis cells.
Area of Science:
- Microbiology
- Molecular Biology
- Virology
Background:
- In vivo phage DNA ejection is an active process involving viral and host proteins.
- Bacteriophage phi29 DNA ejection occurs in two steps: an initial push and a subsequent pull.
- Protein p17, ejected during the first step, is known to be required for the second DNA pull step.
Purpose of the Study:
- To investigate the role of membrane protein p16.7 in the DNA ejection mechanism of Bacillus subtilis bacteriophage phi29.
- To determine if p16.7 is involved in the active pulling step of phage DNA entry.
Main Methods:
- Analysis of bacteriophage phi29 DNA ejection in the presence and absence of functional p16.7.
- Investigating the requirement of p16.7 for the second DNA pull step.
Main Results:
- The study demonstrates that protein p16.7 is required for efficient execution of the second DNA pull step.
- This finding indicates a dual role for p16.7, beyond its known function in membrane-associated DNA replication.
Conclusions:
- Bacteriophage phi29 DNA ejection is an active, protein-mediated process.
- Membrane protein p16.7 plays a critical role in the efficient completion of phage DNA entry into the host cell.
Related Concept Videos
DNA Bacteriophages
Viral Replication: Lytic Cycle
Restarting Stalled Replication Forks
The Replisome
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
The Replisome
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
Lytic Cycle of Bacteriophages

