FLP Recombinase and Yeast DNA Replication: Solving the 2 micron Plasmid Problem

  • Thread starter whamola411
  • Start date
In summary, the Flp system utilizes site-specific recombination to increase the copy number of the 2 micron plasmid in a timely manner, overcoming the issue of a short initiation window for DNA replication in yeast cells.
  • #1
whamola411
13
0
This problem talks about the 2 micron plasmid of s. cerivisiae. The yeast cell cycle has a limited time during which initiation of DNA replication can occur. This initiation window is too short to allow the plasmid to undergo several serial replications. The flp system provides a mechanism whereby the copy number of the plasmid can be rapidly increased with one replication initiation event. Show that this is so by observing what happens if flp recombination occurs shortly after replication has begun. Specifically, follow the consequences of recombination between one flp site that has just been replicated and a second site that is still ahead of the DNA replication fork. Look at what happens as the fork advances. Describe this. How does it solve the replication initiation problem described above

I am pretty lost on this. My only idea is that if recombination occurs just after replication it can utilize a rolling circle mechanism. Otherwise, if it starts ahead of the fork, it wouldn't. Thanks for your help!
 
Physics news on Phys.org
  • #2
The Flp system works by using a specific type of recombination called site-specific recombination. This process involves the recognition and exchange of two specific sequences (known as flp sites) located on the same plasmid molecule. When replication occurs, the two flp sites are replicated along with the plasmid's DNA. As the replication fork advances, one of the flp sites is copied and the other one remains ahead of the fork. When the two flp sites come into contact, they recombine, creating a circle of DNA that can then be replicated again. By replicating the plasmid in this way, the copy number of the plasmid can be rapidly increased with one replication initiation event, thus solving the problem of the limited time during which initiation of DNA replication can occur.
 

FAQ: FLP Recombinase and Yeast DNA Replication: Solving the 2 micron Plasmid Problem

What is FLP recombinase and how does it solve the 2 micron plasmid problem?

FLP recombinase is an enzyme that is commonly used in genetic engineering to manipulate DNA sequences. In the context of yeast DNA replication, FLP recombinase is used to specifically target and remove the 2 micron plasmid, a large circular piece of DNA that can cause instability and hinder proper replication of the yeast genome. By cutting and recombining specific DNA sequences, FLP recombinase can effectively remove the 2 micron plasmid and restore stability to the yeast DNA replication process.

What is the 2 micron plasmid and why is it a problem in yeast DNA replication?

The 2 micron plasmid is a large circular piece of DNA that is found in many strains of yeast. It is not essential for survival, but can replicate independently from the yeast genome and be passed down to daughter cells during cell division. This can lead to an excess of plasmids in the cell, which can cause instability and interfere with proper replication of the yeast DNA. This can result in mutations and other genetic abnormalities, making the 2 micron plasmid a problem in yeast DNA replication.

How does FLP recombinase specifically target the 2 micron plasmid?

FLP recombinase recognizes specific DNA sequences, called FLP recognition targets (FRTs), that are present on both the 2 micron plasmid and the yeast genome. By binding to these FRTs, FLP recombinase can cut and recombine the DNA, effectively removing the plasmid from the yeast genome. This specificity allows FLP recombinase to target and remove the 2 micron plasmid without affecting other essential DNA sequences.

What are some potential applications of using FLP recombinase to solve the 2 micron plasmid problem?

One potential application is in the production of recombinant proteins in yeast. The 2 micron plasmid can carry genes that encode for specific proteins, so by removing the plasmid, researchers can control which proteins are being produced by the yeast. This can be useful for studying the function of certain proteins or for producing large quantities of a specific protein for research or therapeutic purposes.

Are there any limitations or drawbacks to using FLP recombinase for solving the 2 micron plasmid problem?

One limitation is that FLP recombinase is only effective in strains of yeast that contain FRTs on both the 2 micron plasmid and the genome. This means that it may not work in all strains of yeast and may not be a universal solution to the 2 micron plasmid problem. Additionally, the process of cutting and recombining DNA can be technically challenging and may require specialized equipment and expertise. However, with proper precautions and techniques, FLP recombinase can be a powerful tool for solving the 2 micron plasmid problem in yeast DNA replication.

Back
Top