Recombinant dna technology-[how are specific genes chosen]?

In summary, recombinant DNA technology involves taking specific segments of DNA from one organism and inserting them into another. Scientists use various methods, such as expression cloning and gene prediction, to determine which portions of DNA regulate specific traits. A famous example is the discovery of the GFP gene in jellyfish, which was later used to label cancer cells. In order to clone the gene, a portion of the sequence was chemically synthesized based on the known amino acid sequence. Another method is expression cloning, which involves determining whether a given sequence is a functional gene.
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ARAVIND113122
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Recombinant dna technology-[how are specific genes chosen]??

IN recombinant dna technology,certain segments of dna are removed from one organism and put in another.How are are specific portions of DNA removed from certain animals and fused into others?? More importantly,how do scientists know which portion of DNA regulates the desired trait-how can they figure this out when there are millions of base pairs??
 
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A famous case is how a gene that makes you glow green was found.

http://gfp.conncoll.edu/prasher.html: Prasher's GFP work was funded by the National Cancer Institute. In his grant he suggested that it should be possible to take the GFP gene out of the jellyfish cell and attach it to cancer cells so that they would be labeled with a fluorescent tag. Prasher managed to find the gene for GFP in Aequorea victoria and was able to express it in bacteria. In 1992, he published a paper in Gene; it reported the cloning of GFP and the sequence of the 238 amino acids in GFP, shown below."

In that case the amino acid sequence was known, from which a portion of the gene sequence was guessed. The guessed sequence was chemically synthesized. The synthesized sequence would bind to the complementary portion of the full gene sequence in a "gene library".

Another way to do it is called expression cloning.
 
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1. How are specific genes chosen for recombinant DNA technology?

Specific genes are chosen based on their function and relevance to the desired outcome. This can involve identifying genes that are responsible for a particular trait or disease, or genes that produce certain proteins or enzymes. Scientists may also use databases and bioinformatics tools to analyze the genetic sequence and identify potential candidate genes.

2. What techniques are used to isolate specific genes for recombinant DNA technology?

The most commonly used techniques to isolate specific genes include polymerase chain reaction (PCR), in which specific segments of DNA are amplified, and restriction enzyme digestion, in which DNA is cut at specific sites. Other techniques such as DNA hybridization and cloning can also be used to isolate specific genes.

3. How are specific genes inserted into a host organism during recombinant DNA technology?

The specific gene of interest is first inserted into a vector, such as a plasmid or virus, which acts as a carrier for the gene. The vector is then introduced into the host organism, where it can replicate and express the desired gene. This process is often done using techniques such as transformation or transfection.

4. What are the potential benefits of using recombinant DNA technology?

Recombinant DNA technology has a wide range of applications, including the production of medicines, vaccines, and genetically modified organisms. It also allows for the study and understanding of gene function and disease mechanisms, and can potentially lead to the development of new treatments and cures for various diseases.

5. Are there any ethical concerns surrounding the use of recombinant DNA technology?

While recombinant DNA technology has many potential benefits, there are also ethical concerns regarding the safety and potential consequences of manipulating genetic material. These concerns include the potential for unintended consequences, unequal access to genetic modifications, and the impact on natural ecosystems. It is important for scientists to consider and address these concerns in their research and applications of recombinant DNA technology.

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