DNA fingerprinting involves identifying differences in some specific regions in DNA sequence, called as
- Polymorphic DNA
- Satellite DNA
- Repetitive DNA
- Single nucleotides
The Correct Option is C
Solution and Explanation
In DNA fingerprinting, specific regions of repetitive DNA sequences, known as minisatellites or microsatellites, are used to identify differences in DNA sequences. These regions are indeed referred to as repetitive DNA.
So, the correct option is (C): Repetitive DNA
Top Questions on Molecular Basis of Inheritance
- Study the items of Column-I and those of Column-II:
Column-I Column-II
(a) RNA polymerase I (i) 18s rRNA
(b) RNA polymerase II (ii) SnRNAs
(c) RNA polymerase III (iii) hnRNA
Choose the option that correctly matches the items of Column-I with those of Column-II:- CBSE CLASS XII - 2025
- Biology
- Molecular Basis of Inheritance
- The RNA triplet UAG acts as a stop codon which terminates the synthesis of a polypeptide. Below is given a strand of DNA which codes for four amino acids.
In which position will an insertion of a thymine nucleotide result in the termination of translation?
DNA strand:
3′ T C C A C C C G A T G C 5′- CBSE CLASS XII - 2025
- Biology
- Molecular Basis of Inheritance
Construct and label a transcription unit from which the RNA segment given below has been transcribed. Write the complete name of the enzyme that transcribed this RNA.
- CBSE CLASS XII - 2025
- Biology
- Molecular Basis of Inheritance
- The base sequence in one of the strands of DNA is: ‘TAGCATGAT’
- Give the base sequence of its complementary strand.
- How are these base pairs held together in DNA molecule?
- Explain the base complementarity rule. Name the scientist who framed this rule.
- CBSE CLASS XII - 2025
- Biology
- Molecular Basis of Inheritance
Student to attempt either option-(A) or (B):
(A) Write the features a molecule should have to act as a genetic material. In the light of the above features, evaluate and justify the suitability of the molecule that is preferred as an ideal genetic material.
OR
(B) Differentiate between the following:- [(i)] Polygenic Inheritance and Pleiotropy
- [(ii)] Dominance, Codominance and Incomplete dominance
- CBSE CLASS XII - 2025
- Biology
- Molecular Basis of Inheritance
Questions Asked in NEET exam
- Consider the diameter of a spherical object being measured with the help of a Vernier Callipers. Suppose its 10 Vernier Scale Divisions (V.S.D.) are equal to its 9 Main Scale Divisions (M.S.D.). The least count in the M.S. is 0.1 cm and the zero of V.S. is at -0.1 cm when the jaws of Vernier callipers are closed. If the main scale reading for the diameter is \(M = 5\) cm and the number of coinciding vernier division is 8, the measured diameter after zero error correction, is:
- NEET (UG) - 2025
- Measurement of length
- De-Broglie wavelength of an electron orbiting in the \(n = 2\) state of hydrogen atom is close to (Given Bohr radius = 0.052 nm):
- NEET (UG) - 2025
- de broglie hypothesis
- Which chromosome in the human genome has the highest number of genes?
- NEET (UG) - 2025
- Human genome
- In a certain camera, a combination of four similar thin convex lenses are arranged axially in contact. Then the power of the combination and the total magnification in comparison to one lens will be, respectively:
- NEET (UG) - 2025
- Images Formed By Lenses
AB is a part of an electrical circuit (see figure). The potential difference \(V_A - V_B\), at the instant when current \(i = 2\) A and is increasing at a rate of 1 amp/second is:
- NEET (UG) - 2025
- Electromagnetic Induction and Inductance
Concepts Used:
DNA Fingerprinting
DNA fingerprinting, also called DNA typing, DNA profiling, genetic fingerprinting, genotyping, or identity testing, in genetics, method of isolating and identifying variable elements within the base-pair sequence of DNA.
The procedure of DNA Fingerprinting:
The procedure for creating a DNA fingerprint consists of first obtaining a sample of cells, such as skin, hair, or blood cells, which contain DNA. The DNA is extracted from the cells and purified. In Jeffreys’s original approach, which was based on restriction fragment length polymorphism (RFLP) technology, the DNA was then cut at specific points along the strand with proteins known as restriction enzymes. The enzymes produced fragments of varying lengths that were sorted by placing them on a gel and then subjecting the gel to an electric current (electrophoresis): the shorter the fragment, the more quickly it moved toward the positive pole (anode). The sorted double-stranded DNA fragments were then subjected to a blotting technique in which they were split into single strands and transferred to a nylon sheet. The fragments underwent autoradiography in which they were exposed to DNA probes—pieces of synthetic DNA that were made radioactive and that bound to the minisatellites. A piece of X-ray film was then exposed to the fragments, and a dark mark was produced at any point where a radioactive probe had become attached. The resultant pattern of marks could then be analyzed.