70 NEET previous-year questions on Molecular Basis of Inheritance, each with the correct answer and a step-by-step solution. Sourced directly from official NEET papers across every booklet code.
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Polio virus
Tobacco mosaic virus
Measles virus
Retrovirus
Solution
The Tobacco mosaic virus (TMV) has a coiled RNA strand and capsomeres. NCERT XII chapter Molecular Basis of Inheritance describes TMV as a rod-shaped virus with a helical arrangement of RNA and protein subunits, so option (b) is correct.
Transcription – Writing information from DNA to t-RNA
Translation – Using information in m- RNA to make protein
Repressor protein – Binds to operator to stop enzyme synthesis
Operon – Structural genes, operator and promoter
Solution
Transcription involves writing information from DNA to mRNA, not tRNA. Translation, repressor proteins, and operons are correctly described in the other options, so option (a) is wrongly matched. NCERT XII chapter Molecular Basis of Inheritance provides these definitions.
Meselson and Stahl
Hershey and Chase
Griffith
Watson and Crick
Solution
Transformation was discovered by Griffith in his experiments with Streptococcus pneumoniae, demonstrating that a heritable factor could be transferred from one bacterium to another. NCERT XII chapter Molecular Basis of Inheritance credits Griffith with this discovery, so option (c) is correct.
DNA enclosed in a protein coat
Prokaryotic nucleus
Single chromosome
Both DNA and RNA
Solution
Viruses typically contain either DNA or RNA enclosed in a protein coat called a capsid. They do not have a prokaryotic nucleus or a single chromosome, and they do not contain both DNA and RNA simultaneously, so option (a) is correct. NCERT XII chapter Molecular Basis of Inheritance describes the structure of viruses.
Pachytene
Zygotene
Diplotene
Diakinesis
Solution
Recombinase enzymes are active during the pachytene stage of prophase I, facilitating crossing over between homologous chromosomes. NCERT XII chapter Molecular Basis of Inheritance describes this process, so option (a) is correct.
5' — 3' 3' —5'
3' — 5' 5' — 3'
5' — 3' 5' — 3'
3' — 5' 3' — 5'
Solution
RNA synthesis occurs in the 5' to 3' direction, while the template DNA strand is read in the 3' to 5' direction. This is consistent with the mechanism of transcription described in NCERT XII Molecular Basis of Inheritance, so option (a) is correct.
Archegonia are found in Bryophyta, Pteridophyta and Gymnosperms
Mucor has biflagellate zoospores
Haploid endoperm is typical feature of gymnosperms
Brown algae have chlorophyll a and c, and fucoxanthin
Solution
Mucor has non-motile spore i.e. sporangiospores
Fatty acids in a diglyceride
Monosaccharides in a polysaccharide
Amino acids in a polypeptide
Nucleic acids in a nucleotide
Solution
Phosphodiester bond is formed between two nucleotides of nucleic acid. www.vedantu.com 13
Chromosome, gene, genome, nucleotide
Genome, chromosomes, nucleotide, gene
Genome, chromosome, gene, nucleotide
Chromosome, genome, nucleotide, gene
Solution
Order of organisation of genetic material
Complementary base pairing
5’ phosphoryl and 3’ hydroxyl ends
Heterocyclic nitrogenous bases
Chargaff’s rule
Solution
Chargaff's rule is applicable only for DNA. www.vedantu.com 4
They lack a protein coat
They are smaller than viruses
They cause infections
Their RNA is of high molecular weight
Solution
In viroids, RNA is of low molecular weight. www.vedantu.com 48
Glucose
Galactose
Lactose
Lactose and galactose
Solution
Lac operon becomes active only after inducing lactose as it is a substrate for the enzyme beta- galactosidase and it also regulates the switching on and off of the operon which cannot be done by glucose and galactose.
(i) and (iv) are correct
(ii) and (iv) are correct
(i), (iii) and (iv) are correct
(i), (ii) and (iii) are correct
Solution
Hemophilia is a sex – linked recessive disease in which there is a problem in clotting of blood. Down’s syndrome (trisomy 21) is caused due to aneuploidy. Phenylketonuria is an autosomal recessive gene disorder. Sickle cell anaemia is autosomal recessive gene disorder.
AUG
UGA
UAA
UAG
Solution
AUG is start codon that codes for methionine whereas UGA, UAA and UAG are stop codons.
Griffith
Hershey and Chase
Avery, Mcleod and McCarty
Hargobind Khorana
Solution
Hershey and Chase gave unequivocal proof which ended the debate between protein and DNA as genetic material.
The leading strand towards replication fork
(2 ) The lagging strand towards replication fork
The leading strand away from replication fork
The lagging strand away from the replication fork
Solution
Two DNA polymerase molecules work simultaneous at the DNA fork, one on the leading strand and the other on the lagging strand. Each Okazaki fragment is synthesized by DNA polymerase at lagging strand in 5′? → 3 ′? direction. New Okazaki fragments appear as the replication fork opens further. As the first Okazaki fragment appears away from the replication fork, the direction of elongation would be away from replication fork.
Plants
Fungi
Animals
Bacteria
Solution
Spliceosomes are used in removal of introns during post-transcriptional processing of hnRNA in eukaryotes only as split genes are absent as prokaryotes.
DNA molecules with protein coat
DNA molecules without protein coat
RNA molecules with protein coat
RNA molecules without protein coat
Solution
Viroids are sub-viral agents as infectious RNA particles, without protein coat.
Transcription is occurring
DNA replication is occurring
The DNA is condensed into a Chromatin Fibre
The DNA double helix is exposed
Solution
The association of H1 protein indicates the complete formation of nucleosome. Therefore the DNA is in condensed form. www.vedantu.com 24
Positively charged
Negatively charged
Neutral
Either positively or negatively charged depending on their size
Solution
DNA fragments are negatively charged because of phosphate group.
1
11
33
333
Solution
If deletion occurs at 901st position the remaining 98 bases specifying for 33 codons of amino acids will be altered.
r-RNA
t-RNA
m-RNA
mi-RNA
Solution
rRNA is most abundant in animal cell. It constitutes 80% of total RNA of the cell.
Spliceosomes take part in translation.
Punnett square was developed by a British scientist.
Franklin S tahl coined the term ‘‘linkage’’.
Transduction was discovered by S. Altman.
Solution
Punnett square was developed by British geneticist Reginald Punnett to predict the outcomes of genetic crosses. NCERT XII chapter Molecular Basis of Inheritance covers the history and development of genetic tools, confirming option (b) as correct.
Plant
Bacterium
Fungus
Virus
Solution
The experimental proof for semiconservative replication of DNA was first shown in bacteria, specifically , by Meselson and Stahl. NCERT XII chapter Molecular Basis of Inheritance describes this experiment, so option (b) is correct.
an enhancer
structural genes
an operator
a promoter
Solution
An operon consists of structural genes, an operator, and a promoter. An enhancer is not part of the operon structure but influences gene expression from a distance. NCERT XII chapter Molecular Basis of Inheritance defines the components of an operon, so option (a) is correct.
ACCUAUGCGAU
UGGTUTCGCAT
AGGUAUCGCAU
UCCAUAGCGUA
Solution
The transcribed mRNA sequence is complementary to the coding strand, with T replaced by U. Thus, AGGTATCGCAT transcribes to UCCAUAGCGUA, but since the mRNA is synthesized from the template strand, the correct sequence is the complement of the coding strand: AGGUAUCGCAU. Option (c) is correct.
Bronchioles and Fallopian tubes
Bile duct and Bronchioles
Fallopian tubes and Pancreatic duct
Eustachian tube and Salivary duct
Solution
Factual NCERT
Chilled Chloroform
Isopropanol
Chilled ethanol
Methanol at room temperature
Solution
Factual NCERT
Geneva Protocol
Montreal protocol
Kyoto Protocol
Gothenburg Protocol
Solution
Ref. XII NCERT Chapter- 16, Page No. 283
Its seeds contain inhibitors that prevent germination.
Its embryo is immature.
It has obligate association with mycorrhizae
It has very hard seed coat.
Solution
Out of NCERT Pinus seed can not germinate until unless mycorrhizal association is not developed.
Cyclical Selection
Directional Selection
Stabilizing Selection
Disruptive Selection
Solution
Average phenotypes are selected in stabilizing selection
Glucocorticoids stimulate gluconeogenesis.
Glucagon is associated with hypoglycemia.
Insulin acts on pancreatic cells and adipocytes.
Insulin is associated with hyperglycemia.
Solution
Glucocorticoids, such as cortisol, stimulate gluconeogenesis, the process of glucose synthesis from non-carbohydrate sources. This is a key function of glucocorticoids as described in NCERT XII Molecular Basis of Inheritance, making option (a) correct.
DNA ligase
DNA helicase
DNA polymerase
RNA polymerase
Solution
DNA helicase is the enzyme that unwinds and separates the DNA strands during transcription. NCERT XII chapter Molecular Basis of Inheritance describes DNA helicase as essential for breaking hydrogen bonds between base pairs, so option (b) is correct.
Binding of mRNA to ribosome
Recognition of DNA molecule
Aminoacylation of tRNA
Recognition of an anti-codon
Solution
The first phase of translation involves the binding of mRNA to the ribosome, initiating the process of protein synthesis. NCERT XII chapter Molecular Basis of Inheritance describes this as the initial step, so option (a) is correct.
Adenine pairs with thymine through two H-bonds.
Adenine pairs with thymine through one H-bond.
Adenine pairs with thymine through three H-bonds.
Adenine does not pair with thymine.
Solution
Adenine pairs with thymine through two hydrogen bonds, as described in the base-pairing rules of DNA structure in NCERT XI chapter Molecular Basis of Inheritance. Therefore, option (a) is correct.
They have RNA with protein coat.
They have free RNA without protein coat.
They have DNA with protein coat.
They have free DNA without protein coat.
Solution
Viroids are infectious agents composed of short strands of naked RNA without a protein coat. NCERT XII chapter Molecular Basis of Inheritance defines viroids as small, circular, single-stranded RNA molecules, so option (b) is correct.
2.0 meters
2.5 meters
2.2 meters
2.7 meters
Solution
The length of the DNA can be calculated using the formula , where is the number of base pairs and is the distance between two consecutive base pairs. Substituting the values, . Therefore, option (c) is correct.
Yellow bands
Bright orange bands
Dark red bands
Bright blue bands
Solution
DNA stained with ethidium bromide appears as bright orange bands when viewed under UV radiation. Ethidium bromide intercalates into the DNA double helix and fluoresces under UV light, so option (b) is correct.
(a)-Replication; (b)-Transcription; (c)-Transduction; (d)-Protein
(a)-Translation; (b)-Replication; (c)-Transcription; (d)-Transduction
(a)-Replication; (b)-Transcription; (c)-Translation; (d)-Protein
(a)-Transduction; (b)-Translation; (c)-Replication; (d)-Protein
Solution
- Replication is the process of DNA making a copy of itself.
- Transcription is the synthesis of RNA from a DNA template.
- Translation is the process of synthesizing proteins from the mRNA.
- Protein is the final product of the central dogma. Option (c) correctly matches these processes.
Transcribes rRNAs (28S, 18S and 5.8S)
Transcribes tRNA, 5s rRNA and snRNA
Transcribes precursor of mRNA
Transcribes only snRNAs
Solution
RNA polymerase III transcribes tRNA, 5S rRNA, and small nuclear RNAs (snRNAs) in eukaryotes. This is detailed in NCERT XII chapter Molecular Basis of Inheritance, making option (b) correct.
mutated gene partially appears on a photographic film.
mutated gene completely and clearly appears on a photographic film.
mutated gene does not appear on a photographic film as the probe has no complimentarity with it.
mutated gene does not appear on photographic film as the probe has complimentarity with it.
Solution
The mutated gene will hybridize with the radioactive probe and appear clearly on a photographic film through autoradiography, as the probe has complementarity with the mutated DNA sequence. This is based on the principle of nucleic acid hybridization described in NCERT XII chapter Molecular Basis of Inheritance, so option (b) is correct.
Satellite DNA
Repetitive DNA
Single nucleotides
Polymorphic DNA
Solution
DNA fingerprinting relies on identifying variations in polymorphic DNA, which are regions that show differences among individuals. NCERT XII chapter Molecular Basis of Inheritance explains that these polymorphisms are used for genetic identification, so option (d) is correct.
T : 20 ; G : 30 ; C : 20
T : 20 ; G : 20 ; C : 30
T : 30 ; G : 20 ; C : 20
T : 20 ; G : 25 ; C : 25
Solution
According to Chargaff's rules, the amount of adenine (A) equals thymine (T), and guanine (G) equals cytosine (C). If A is 30%, then T is also 30%. The total percentage of G and C is 40%, so G and C are each 20%. Therefore, option (c) is correct.
Okazaki sequences
Palindromic Nucleotide sequences
Poly
tail sequences 24 M1 Section - B (Biology : Zoology)
Solution
Endonucleases recognize and cut DNA at specific palindromic nucleotide sequences, which are sequences that read the same forwards and backwards. NCERT XII chapter Molecular Basis of Inheritance explains that restriction endonucleases identify these palindromic sequences to make precise cuts, so option (b) is correct.
mRNA
tRNA
rRNA
siRNA
Solution
siRNA (small interfering RNA) is not directly involved in protein synthesis. mRNA, tRNA, and rRNA are essential components of the translation process, as described in NCERT XII chapter Molecular Basis of Inheritance, so option (d) is correct.
DNA dependent DNA polymerase
DNA dependent RNA polymerase
DNA Ligase
DNase
Solution
DNA dependent RNA polymerase is the only enzyme that catalyzes the initiation, elongation, and termination of transcription in prokaryotes. NCERT XII chapter Molecular Basis of Inheritance describes this enzyme as essential for the entire transcription process, so option (b) is correct.
Both Statement I and Statement II are true
Both Statement I and Statement II are false
Statement I is correct but Statement II is false
Statement I is incorrect but Statement II is true
Solution
Statement I is incorrect because the codon ‘AUG’ codes only for methionine, not phenylalanine. Statement II is correct as both ‘AAA’ and ‘AAG’ codons code for the amino acid lysine, according to the genetic code table in NCERT XII Molecular Basis of Inheritance, so option (d) is correct.
The small subunit of ribosome encounters mRNA
The larger subunit of ribosome encounters mRNA
Both the subunits join together to bind with mRNA
The tRNA is activated and the larger subunit of ribosome encounters mRNA
Solution
When the small subunit of ribosom e encounters an mRNA, the process of translation of the mRNA to protein begins. This process is followed by the binding of bigger/larger subunit. t-RNA is activated by the addition of amino acid prior to the attachment of ribosome, in the first phase.
Genetic mapping
DNA finger printing
Both genetic mapping and DNA finger printing
Translation
Solution
Polymorphism in DNA sequence is the basis of genetic mapping of human genome as well as of DNA fingerprinting.
3. 3× bp 109
6. × 610bp 9
3. 3× bp 106
6. 6× bp 106
Solution
Number of base pairs × distance between 2 consecutive base pairs = Length of DNA molecule x · 0.34 × 10–9 m = 1.1 m 9 1.1x 0.3 10 −= × = 3.6 × 109 ; 3.3 × 109 bp
20 cells
40 cells
60 cells
80 cells
Solution
From 10 parent E.coli cells 1st generation Therefore, after 60 minutes, 60 E.coli cells will have DNA totally free from 15N.
Bright orange colour
Bright red colour
Bright blue colour
Bright yellow colour
Solution
Upon exposure to UV radiation, DNA stained with ethidium bromide fluoresces a bright orange color. This is due to the intercalation of ethidium bromide into the DNA double helix, enhancing its fluorescence, as described in NCERT XII Molecular Basis of Inheritance, so option (a) is correct.
Wilkins and Franklin
Frederick Griffith
Alfred Hershey and Martha Chase
Avery, Macleoid and McCarthy
Solution
Alfred Hershey and Martha Chase provided unequivocal proof that DNA is the genetic material through their bacteriophage infection experiments. NCERT XII chapter Molecular Basis of Inheritance highlights their work as a key piece of evidence, so option (c) is correct.
Certain important expressed genes.
All genes that are expressed as RNA.
All genes that are expressed as proteins.
All genes whether expressed or unexpressed.
Solution
Expressed Sequence Tags (ESTs) are short subsequences of transcribed cDNA, representing all genes that are expressed as RNA. NCERT XII chapter Molecular Basis of Inheritance defines ESTs as partial sequences of cDNA, so option (b) is correct.
Transcription of only snRNAs
Transcription of rRNAs (28S, 18S and 5.8S)
Transcription of tRNA, 5 srRNA and snRNA
Transcription of precursor of mRNA
Solution
RNA polymerase III is responsible for the transcription of tRNA, 5S rRNA, and snRNA in eukaryotes. This is detailed in NCERT XII chapter Molecular Basis of Inheritance, making option (c) correct.
Repressor, Operator gene, Structural gene
Structural gene, Transposons, Operator gene
Inducer, Repressor, Structural gene
Promotor, Structural gene, Terminator
Solution
A transcription unit of DNA is defined primarily by the three regions in the DNA: (i) A promoter (ii) The structural gene (iii) A terminator The promoter is said to be located towards 5 ′-end (upstream) of the structural gene (the reference is made with respect to the polarity of coding strand) The terminator is located towards 3′-end (downstream) of the coding strand. - 48 - NEET (UG)-2024 (Code-Q1)
8 bp
6 bp
4 bp
10 bp
Solution
The correct answer is option (2). The first restriction endonuclease – Hind II, whose functioning depends on a specific DNA nucleotide sequence was isolated. It was found that Hind II always cut DNA molecules at a particular point by recognising sequence of six base pairs. Option (1), (3) and (4) are incorrect because they have either more than 6 or less than 6 bp.
A-III, B-II, C-I, D-IV
A-III, B-IV, C-I, D-II
A-II, B-III, C-IV, D-I
A-IV, B-I, C-II, D-III
Solution
Frederick Griffith series of experiment witness miraculous transformation in the bacteria. The elucidation of Lac operon was a result of a close association between geneticist, Francois Jacob and a biochemist, Jacques Monod. Meselson and Stahl gave semi-conservative mode of DNA replication. Har Gobind Khorana developed chemical method to define combination of bases in genetic code.
The DNA dependent DNA polymerase catalyses polymerization in one direction that is 3’ → 5’
The DNA dependent RNA polymerase catalyses polymerization in one direction, that is 5’ → 3’
The DNA dependent DNA polymerase catalyses polymerization in 5’ → 3’ as well as 3’ → 5’ direction
The DNA dependent DNA polymerase catalyses polymerization in 5’ → 3’ direction
Solution
In Prokaryotes, like E.coli during replication, the DNA dependent DNA polymerase catalyse polymerization only in one direction, that is 5’ → 3’ ZOOLOGY SECTION-A
5’AUGUACCGUUUAUAGGUAAGU3’
5’AUGUAAAGUUUAUAGGUAAGU3’
5’AUGUACCGUUUAUAGGGAAGU3’
5’ATGTACCGTTTATAGGTAAGT3’
Solution
Template DNA is : 3’TACATGGCAAATATCCATTCA5’ 5’AUGUACCGUUUAUAGGUAAGU3’ m-RNA
Both statement I and statement II are correct
Both statement I and statement II are incorrect
Statement I is correct but statement II is incorrect
Statement I is incorrect but statement II is correct
Solution
In RNA world, RNA was the first genetic material as there are enough evidences to suggest that essential life processes (such as metabolism, translation, splicing, etc) evolved around RNA. RNA used to act as a genetic material as well as catalyst (there are some important biochemical reaction in living systems that are catalysed by RNA catalysts not by protein enzymes) so, statement I is correct statement II is also correct as DNA being double stranded and having complementary strands further resists changes by evolving a process of repair.
Chromosome X
Chromosome Y
Chromosome 1
Chromosome 10
Solution
Chromosome 1 has the highest number of genes in the human genome, with over 2000 genes. NCERT XII chapter Molecular Basis of Inheritance provides this information, making option (c) correct.
Both statement I and statement II are correct
Both statement I and statement II are incorrect
Statement I is correct but statement II is incorrect
Statement I is incorrect but statement II is correct
Solution
Both transfer RNAs and ribosomal RNA interact with mRNA.
RNA interference (RNAi) takes place in all eukaryotic organisms as a method of cellular defence.
A, B, C only
B, C, D only
B, C, E only
C, D, E only
Solution
Post-transcriptional events in eukaryotic cells include the removal of introns and joining of exons (splicing), addition of a methyl group at the 5' end (capping), and addition of adenine residues at the 3' end (polyadenylation). Base pairing of two complementary RNAs is not a post-transcriptional event, so option (b) is correct.
Both statement I and statement II are correct
Both statement I and statement II are incorrect
Statement I is correct but statement II is incorrect
Statement I is incorrect but statement II is correct
Solution
The cutting of DNA by restriction endonucleases results in the fragments of DNA. These fragments can be separated by a technique known as gel electrophoresis.
The separated bands of DNA are cut out from the agarose gel and extracted from the gel piece. This step is known as elution. The DNA fragments purified in this way are used in constructing rDNA by joining them with cloning vectors.
• In gel electrophoresis, the DNA fragments separate (resolve) according to their size through sieving effect provided by the agarose gel. Hence, the smaller the fragment size, the farther it moves from cathode towards anode.
Complementary dsRNA
Inhibitory ssRNA
Complementary tRNA
Non-complementary ssRNA
Solution
RNAi (RNA interference) takes place in all eukaryotic organisms as a method of cellular defense. This method involves silencing of a specific mRNA due to a complementary dsRNA molecule that binds to and prevents translation of the mRNA.
A-IV, B-II, C-I, D-III
A-IV, B-III, C-I, D-II
A-III, B-II, C-IV, D-I
A-II, B-IV, C-I, D-III
Solution
- Alfred Hershey and Martha Chase confirmed DNA as the genetic material (IV).
- Euchromatin is loosely packed and light-stained (III).
- Frederick Griffith worked with (I).
- Heterochromatin is densely packed and dark-stained (II).
George Gamow
Francis Crick
Jacque Monod
Franklin Stahl
Solution
George Gamow, a physicist proposed that genetic code for amino acids should be made up of three nucleotides.
Transport of pre-mRNA to cytoplasm prior to splicing.
Removal of introns and joining of exons.
Addition of methyl group at 5′ end of hnRNA.
Addition of adenine residues at 3′ end of hnRNA.
Solution
The process of copying genetic information from one strand of the DNA into RNA is known as transcription. It occurs in the cytoplasm with the help of transcribing enzyme.
Transport of pre-mRNA to cytoplasm prior to splicing is a part of transcription.
The primary transcript is converted into functional mRNA after post transcriptional processing involves 3 steps as follows-
• Modification of 5′ end by capping,
• Tailing,
• Splicing.
Base pairing of two complementary RNA is not on event of post-transcription. Hence, statements B, C, D are post-transcriptional modification events in eukaryotic cell.
(alpha)
(sigma)
(rho)
(gamma)
Solution
The (rho) factor is a protein that plays a crucial role in the termination of transcription by facilitating the dissociation of the RNA polymerase from the DNA template. NCERT XII chapter Molecular Basis of Inheritance describes the function of the factor in transcription termination, so option (c) is correct.
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