Related Experiment Video
Updated: Jul 2, 2025

06:12
Production of Double-stranded DNA Ministrings
Published on: February 29, 2016
10.4K
Loop extrusion-mediated plasmid DNA cleavage by the bacterial SMC Wadjet complex.
Biswajit Pradhan1, Amar Deep2, Jessica König1
1Max Planck Institute of Biophysics, 60438 Frankfurt am Main, Germany.
Biorxiv : the Preprint Server for Biology
|February 26, 2024
Summary
Wadjet, a bacterial SMC complex, uses DNA loop extrusion to recognize and cleave circular plasmids. This mechanism is crucial for bacterial defense against foreign DNA.
Area of Science:
- Molecular Biology
- Genetics
- Microbiology
Background:
- Structural Maintenance of Chromosomes (SMC) complexes are vital for genome organization in all life forms.
- Bacterial Wadjet complexes, similar to MukBEF, defend against plasmid transformation.
- Previous studies showed Wadjet cleaves circular DNA, but the mechanism was unknown.
Approach:
- Utilized in vitro single-molecule imaging to observe Wadjet's DNA interaction.
- Visualized DNA loop extrusion and plasmid cleavage dynamics.
- Investigated the role of the dimeric JetABC supercomplex and JetC motor subunits.
Key Points:
- Wadjet functions as a symmetric DNA loop extruder, coiling DNA from both sides.
- Loop extrusion requires a dimeric JetABC supercomplex with two JetC motor dimers.
- Wadjet extrudes entire plasmids, stalls, and then cleaves the DNA.
Conclusions:
- DNA loop extrusion is key to Wadjet's plasmid recognition and elimination.
- This study reveals a novel defense mechanism in bacteria.
- Loop extrusion is an evolutionarily conserved process among SMC complexes.
Related Concept Videos
The Replisome
33.5K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or 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 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...
33.5K
Homologous Recombination
50.5K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.5K
Mismatch Repair
4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.8K
DNA Isolation
39.1K
DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
39.1K
Single-Strand DNA Binding Proteins
14.1K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
14.1K
Replication in Prokaryotes
24.9K
DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...
24.9K

