DNA Fingerprinting – Introduction, Principles, Process

A laboratory procedure known as "DNA fingerprinting" is used to infer a person's likely identification from the nucleotide sequences. Check this article to know all about DNA Fingerprinting.

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DNA Fingerprinting

DNA fingerprinting is a chemical test that reveals a person’s or another living thing’s genetic makeup. It is employed to locate blood relatives, identity remains present evidence in court, and discover medical treatments. The importance of DNA fingerprinting is explained in this article.

 DNA analysis has been one of the most significant scientific advancements in criminal investigation since fingerprinting was invented a century ago.

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Introduction

Chemical testing, known as DNA fingerprinting, shows the genetic makeup of a human or other living entity. It is used as evidence in court to discover blood relatives, identify remains, and look for medical treatments.

A method for extracting and detecting variable components within the base-pair sequence of DNA is known as DNA fingerprinting in genetics. It is sometimes called DNA profiling, genotyping, genetic fingerprinting, or identification testing.

Creating a DNA fingerprint takes a sample of DNA-containing cells, such as skin, hair, or blood cells, and observes that specific regions of highly variable DNA that do not affect how genes function are repeated within genes. The DNA is then separated and removed from the cells.

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Principle of DNA Fingerprinting 

 Numerous short, repeatable non-coding sequences that can be inherited make up the human genome. They are called satellite DNA because they may be isolated from the bulk DNA using density gradient centrifugation.

They can be classified as either microsatellites or microsatellites depending on the length, base makeup, and tandemly repeating units. The foundation of DNA fingerprinting is polymorphism, which these satellite DNAs exhibit.

Variable number tandem repeats (VNTRs) and short tandem repeats are two categories for the repeat regions based on the size of the repeats. Every person receives these repeats from their parents, which are genetic markers. As a result, every person has a unique composition of VNTRs, and this is how the DNA fingerprinting approach works.

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DNA Fingerprinting Steps:

  • DNA isolation
  • Restriction endonuclease digestion of DNA
  • DNA fragment separation using electrophoresis,
  • DNA fragments that have been isolated are transferred (blotted) to synthetic membranes such as nitrocellulose or nylon,
  • Employing a labeled VNTR probe to hybridise, and using autoradiography to find the hybridised DNA fragments.

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DNA Fingerprinting Process

Significant improvements include sample collection, DNA extraction, absorption or intensification, and inquiry findings.

Stage 1: Sample Collection 

 DNA can be extracted from any physiological fluid or material. Significant samples include buccal smears, saliva, blood, amniotic fluid, chorionic villi, skin, hair, bodily fluid, and various tissues.

Stage 2: DNA Extraction

First, we must obtain DNA. One of the most important developments in DNA extraction, which is essential for any genetic applications. Excellent DNA quantity and quality increase the likelihood of obtaining better results.

 You can use the DNA extraction techniques listed below,

  •  Strategy for DNA extraction using phenol-chloroform
  •  DNA extraction method using CTAB
  •  DNA extraction with proteinase K

However, for DNA fingerprinting, we strongly advise using a ready-to-use DNA extraction kit. To conduct the DNA test, the purity and quantity of DNA must be 1.80 and 100ng, respectively. If necessary, use the DNA sanitisation equipment to filter the DNA. From that point on, use the UV-visible spectrophotometer to quantify the DNA.  

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Stage 3: DNA sequencing, enhancement, or restriction absorption

 There are three common tactics used:

  • RFLP-based STR analysis
  • PCR-based analysis
  • Real-time PCR analysis

Stage 4: Results Analysis

As we looked at, different DNA profiling results might be obtained using southern blotting, agarose gel electrophoresis, narrow electrophoresis, continuing intensification, and DNA sequencing, where rt-PCR and sequencing are largely used in forensic science.

Stage 5: Interpreting the outcomes 

It is possible to identify differences and similarities between people by examining the DNA profiles of various examples. Amazingly, the entire process is now almost automatic. We don’t need to do anything because the computer provides definitive results.

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Applications

The DNA fingerprinting technique can evaluate a person’s innate personality. There is no superior alternative to DNA fingerprinting for character approval. Body parts that have been gravely injured can be identified. It is used to find contaminated maternal cells.

Maternal cell tainting is one of the main drawbacks of prenatal diagnosis. Maternal DNA or tissue can sometimes be found in the amniotic fluid or CVS test. False-positive results may increase with contamination, especially because of carrier identification. During pregnancy genetic testing, maternal cell tainting can be identified using VNTRs and STRs markers with PCR-gel electrophoresis.

Analysing crime scenes and criminal checks is one of the most important applications of the current strategy. The illustration is taken from the crime scene and may include saliva, blood, hair follicles, or semen. The two previously described markers are used to analyse the suspect’s DNA and compare it to the sample. The identities of criminals involved in a crime can be compiled by coordinating DNA band designs.

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Blood-Typing as a Method for Paternity Tests

Alec Jeffreys first developed the technique for DNA fingerprinting in 1984, and it became available for paternity testing in 1988. Blood classifications were the most popular computation for human paternity testing before this DNA inquiry was available.

Blood bunches are a common example of how Mendelian genetic traits operate. All things considered, countless alleles are present in different human blood groups, and these alleles exhibit various prevalence patterns.

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DNA fingerprinting in agriculture

A few DNA minisatellite tests have produced component profiles that are useful for work on plant reproduction. When vegetative spread material is broken down, the part profiles are uniform. Additionally, samples from animals that self-inbreed have the same profiles. Interestingly, hereditary recombination results in unusually variable, typically single, explicit component profiles in cross-pollinating species.

Along these lines, different cultivars can be identified, and genotypes of wild species in distinct populations can also be. As was recently said for apples and rice, these component profiles can also be employed for parentage analysis, allowing us to identify the origin of incorrectly documented cultivars.

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Additionally, analyses of hereditary variety-dependent similitude lists derived from section profiles reveal close ties with known degrees of hereditary relatedness.

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India’s use of DNA fingerprinting

The Department of Biotechnology, Ministry of Science and Technology, Government of India, operates the Centre for DNA Fingerprinting and Diagnostics (CDFD), a biotechnology research facility in Hyderabad, India.

According to Article 51A(h) and (j) of the Constitution, citizens are responsible for cultivating a scientific mindset, a humanistic outlook, and a spirit of inquiry and reform to pursue excellence in individual and group endeavors. In this way, the parliament can rightfully undertake and promote technical and scientific methods to speed up the criminal justice system as specified under the union list.

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The “facts necessary to explain or introduce a fact in the dispute or relevant fact” are covered under Section 9 of the Indian Evidence Act of 1872.

In exceptional circumstances, such as rape, the CrPC’s Section 53-A allows a rape suspect to undergo a medical examination, which may entail the collection of the suspect’s body fluids for DNA fingerprinting.

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What procedures make up DNA fingerprinting?

Extraction, quantification, amplification, and capillary electrophoresis are the primary procedures in DNA testing.

The development of DNA fingerprinting: why?

Alec Jeffreys created DNA fingerprinting after realising that minisatellites can be used to identify differences in human DNA. DNA fingerprinting is now used to identify distinctive patterns in people and for various purposes, including identifying bodies and providing evidence in court.

What is the purpose of DNA fingerprinting?

DNA fingerprinting is a method for locating and analysing the differences in different people's DNA. Application In forensic science, it is used to pinpoint prospective criminal suspects.

Who made the first DNA fingerprint?

DNA-based identity testing was not widely used until it was invented by Sir Alec Jeffreys, a professor and geneticist at the University of Leicester in the United Kingdom (UK) 20 years ago.

What are the two categories of DNA fingerprinting?

There are two accepted techniques for DNA fingerprinting:

PCR of VNTR-containing DNA.
South blotting (using RFLPs).

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