Explain how the process of RNA interference technology is used effectively to prevent infestation of the roots of tobacco plant by the nematode Meloidogyne incognita. OR
Explain how more than a billion copies of a fragment of DNA are formed using the technique of PCR.
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RNA interference uses double-stranded RNA to silence genes, while PCR uses repeated cycles of heating and cooling to exponentially amplify DNA fragments.
In this method, specific genes responsible for nematode infestation are silenced.
The nematode Meloidogyne incognita affects tobacco plant roots.
To counter this, a DNA sequence producing both sense and antisense RNA strands for the nematode’s essential genes is introduced into the plant using Agrobacterium vectors.
These complementary RNA strands form double-stranded RNA (dsRNA) inside the host plant cells.
The dsRNA triggers the RNA interference (RNAi) mechanism, degrading the nematode’s specific mRNA.
As a result, the target gene is silenced, protecting tobacco plants from nematode attack.
Polymerase Chain Reaction (PCR) Process:
PCR is a technique to amplify a specific segment of DNA.
The process involves multiple cycles of:
Denaturation: Double-stranded DNA is heated to separate into single strands.
Annealing: Primers bind to the specific target sequences.
Extension: DNA polymerase extends primers to synthesize new DNA strands.
Each cycle doubles the DNA quantity.
Repeating this process for around 30 cycles results in over a billion copies of the desired DNA fragment.