RFLP | Zoology Optional Notes for UPSC PDF Download

Principle of Restriction Fragment Length Polymorphism (RFLP)


If two organisms differ in the distance between sites of cleavage of a particular restriction endonuclease, the length of the fragments produced will differ when the DNA is digested with a restriction enzyme. The similarity and differences of the patterns thus generated can be used to differentiate species (and even strains) from one another.

Steps Involved in Restriction Fragment Length Polymorphism (RFLP)


RFLP | Zoology Optional Notes for UPSC

  • The first step in this process is to isolate the DNA from the target.
  • Once the the DNA is isolated from the sample it is subjected to restriction digestion using restriction enzymes.
  • The digested DNA sample is then subjected to gel electrophoresis, in which the DNA is separated based on its size. Many DNA fragments with slight differences in length are produced.
  • The gel is then exposed to a chemical to denature double-stranded DNA to become single- stranded.
  • This is followed by southern blotting where DNA is transferred from gel to nylon membrane.
  • The nylon membrane is then exposed to solution with radioactive complementary nucleotide probes that hybridize to specifically chosen DNA sequences on nylon membrane.
  • The membrane is then placed against X- ray film, where hybridized radioactive probes cause exposure of X-ray film, producing an autoradiogram.
  • RFLP analysis is carried out to detect differences in pattern to confirm polymorphisms.

Applications of Restriction Fragment Length Polymorphism (RFLP)


RFLP analysis was formerly an important tool in genome mapping, localization of genes for genetic disorders, determination of risk for disease, and paternity testing.

RFLP can be used in many different settings to accomplish different objectives:

  • In paternity cases or criminal cases to determine the source of a DNA sample. (i.e. it has forensic applications).
  • Determining the disease status of an individual. (e.g. it can be used in the detection of mutations)
  • To measure recombination rates which can lead to a genetic map with the distance between RFLP loci.
  • In the characterization of genetic diversity or breeding patterns in animal populations.
  • RFLP has been developed for chromosomes mapping of humans, mice, maize, tomato, rice, etc.

Advantages of Restriction Fragment Length Polymorphism (RFLP)


  • The main advantage of RFLP analysis over PCR-based protocols is that no prior sequence information, nor oligonucleotide synthesis, is required.
  • Results are based on reliable genotypic characteristics’ rather than on phenotypes.
  • RFLP based Genetic Marker
  • RFLP is the co dominant marker thus can estimate heterozygosity.
  • RFLP & is very useful study in Genomic DNA Sequence. 
  • Highly robust methodology with good transferability between laboratories.

Limitations of Restriction Fragment Length Polymorphism (RFLP)


  • Slow
  • Cumbersome
  • Requires a large amount of sample DNA.
  • Automation not possible
  • Low levels of polymorphism in some species
  • Few loci detected per assay
  • Need a suitable probe library
  • Needing the combined process of probe labeling, DNA fragmentation, electrophoresis, blotting, hybridization, washing, and autoradiography.
The document RFLP | Zoology Optional Notes for UPSC is a part of the UPSC Course Zoology Optional Notes for UPSC.
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FAQs on RFLP - Zoology Optional Notes for UPSC

1. What is the principle of Restriction Fragment Length Polymorphism (RFLP)?
Ans. Restriction Fragment Length Polymorphism (RFLP) is a technique used in molecular biology to analyze variations in DNA sequences. It is based on the fact that different individuals have variations in the DNA sequences recognized by restriction enzymes. RFLP involves cutting DNA using restriction enzymes and then separating the resulting fragments based on their length using gel electrophoresis.
2. What are the steps involved in Restriction Fragment Length Polymorphism (RFLP)?
Ans. The steps involved in Restriction Fragment Length Polymorphism (RFLP) are as follows: 1. DNA extraction: DNA is extracted from the cells or tissues of interest. 2. Digestion: The extracted DNA is digested with restriction enzymes that recognize specific DNA sequences. 3. Gel electrophoresis: The digested DNA fragments are separated based on their size using gel electrophoresis. 4. DNA visualization: The separated DNA fragments are visualized using techniques like staining or radioactive labeling. 5. Analysis: The DNA banding patterns are analyzed to identify variations in DNA sequences among different individuals.
3. What are the applications of Restriction Fragment Length Polymorphism (RFLP)?
Ans. The applications of Restriction Fragment Length Polymorphism (RFLP) include: 1. Genetic mapping: RFLP can be used to map the location of genes on chromosomes. 2. Forensics: RFLP can be used to analyze DNA evidence in criminal investigations. 3. Paternity testing: RFLP can be used to determine biological relationships between individuals. 4. Disease diagnosis: RFLP can be used to identify genetic variations associated with certain diseases. 5. Evolutionary studies: RFLP can be used to study genetic variations within and between species.
4. What are the advantages of Restriction Fragment Length Polymorphism (RFLP)?
Ans. The advantages of Restriction Fragment Length Polymorphism (RFLP) include: 1. High resolution: RFLP can detect small variations in DNA sequences. 2. Cost-effective: RFLP does not require expensive equipment and is relatively inexpensive compared to other DNA analysis techniques. 3. Established technique: RFLP has been widely used and validated in various fields of molecular biology. 4. No prior knowledge of DNA sequence: RFLP can detect genetic variations without prior knowledge of the specific DNA sequence. 5. Long-term stability: RFLP results can be stored and reanalyzed in the future.
5. What are the limitations of Restriction Fragment Length Polymorphism (RFLP)?
Ans. The limitations of Restriction Fragment Length Polymorphism (RFLP) include: 1. Time-consuming: The RFLP technique requires several steps and may take a significant amount of time to obtain results. 2. Low throughput: RFLP is not suitable for high-throughput analysis due to its labor-intensive nature. 3. Limited genetic information: RFLP can only detect variations in specific DNA sequences recognized by restriction enzymes. 4. Inability to detect single nucleotide polymorphisms (SNPs): RFLP is not sensitive enough to detect single nucleotide changes in DNA sequences. 5. Requirement for high-quality DNA: RFLP requires high-quality DNA samples, which can be challenging to obtain from degraded or low-yield sources.
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