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NEET 2022 | Class 12

NEET Important Chapter - Molecular Basis of Inheritance

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Molecular Basis of Inheritance

Molecular Basis of Inheritance


Last updated date: 12th Dec 2024
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Introduction

This document contains the chapter named molecular basis of inheritance as per the NEET syllabus for biology. It will be fruitful for NEET aspirants who are looking for the last minute revision of the chapter. 


The following document contains all of the important topics and provides the insight of the exam pattern. By going through this document, one can find out all the answers to the important questions related to the chapter such as why DNA acts as the genetic material, what is the central dogma of biology, what is DNA replication, who gave the structure of DNA, etc.


Important Topics of Molecular Basis of Inheritance

  • The search for genetic material 

  • Structure of polynucleotide chain

  • Double-Helix model of DNA

  • Packaging of DNA

  • Central dogma of biology

  • DNA replication

  • Transcription

  • Genetic code

  • Translation

  • Regulation of gene expression:Lac operon

  • Human genome project

  • DNA fingerprinting


Important Concepts

Search for Genetic Material

There were varieties of experiments that had been performed by the different scientists to answer the question of what molecule was actually the genetic material. The list  and the overall conclusion of the experiments are given in the table below.

Name of the Experiment

Performed (by & in)

Summary

Transforming Principle

Frederick Griffith, 1928

In this experiment, Griffth concluded that in the infected mice, some “transforming principle” gets transferred from heat-killed S-strain of Streptococcus pneumoniae to R-strain and this enables them to make the smooth polysaccharide coat which enables them to become virulent. This may be due to the transfer of the genetic material. However, the bio-chemical nature of genetic material was unknown. 

Biochemical Characterization of Transforming Principle

Oswald Avery, Colin MacLeod & Maclyn McCarty, 1933-34

The gap i.e. biochemical nature of the transforming principle was filled in this experiment. They also discovered that only the DNA is responsible for the transformation.

Hershey & Chase  experiment

Hershey & Chase,1952

They found that the bacteria which were infected with viruses that had radioactive DNA were radioactive, indicating that DNA was the material that passed from the virus to the bacteria while the bacteria that were infected with viruses that had radioactive proteins were not radioactive, which indicates that proteins did not enter the bacteria from the viruses. Hence, it is the DNA which acts as the genetic material.


Structure of Polynucleotide Chain

Each nucleotide consists of three components that are listed below.

1. Nitrogenous Bases: They are of two categories such as:

Purines: It includes Adenine(A) and Guanine (G). Both the purines are present in the case of DNA as well as in RNA.

Pyrimidines: It includes Cytosine(C) and Thymine(T) in the case of  DNA and Cytosine(C) and Uracil(U) in RNA.

2. Sugar: In the case of nucleotides, pentose sugar is present i.e. Ribose sugar in case of  RNA and deoxyribose sugar in case of DNA.

3. Phosphate-group: It plays an important role in the formation of sugar-phosphate back-bone that acts as the structural framework of the nucleic acids.

Structure of Polynucleotide Chain

  • Nucleoside: It consists of a nitrogenous base and the sugar.

  • Nucleotide: It consists of a nitrogenous base, sugar, and the phosphate group.


The Structural Difference Between Nucleotide and Nucleoside


Trick: In the nucleoside, the phosphate group is kept aside.


Double-Helix Model of DNA

This model describes the structure of DNA. It was given by Watson & Crick in 1953. According to this model, two polynucleotide chains make DNA, where the backbone consists of sugar-phosphate and nitrogenous bases are present towards the inside. Both the chains run opposite to each other in terms of polarity i.e. one with 5’→3’ end and the other one with  3’→5’ end. Purine always pairs with pyrimidine with the help of hydrogen bonds (A to T or U  with 2 hydrogen bonds, C to G with three hydrogen bonds).

Structure of DNA

Chargaff’s Rule

It states that in the DNA, there is always equality in quantity between the bases A and T and between the bases G and C.


DNA

RNA

It stands for deoxy-ribonucleic acid and consists of deoxyribose sugar and phosphate backbone having four distinct nitrogenous bases such as adenine, thymine cytosine, and guanine.

It stands for ribo-nucleic acid and consists of ribose and phosphate backbone with four varying nitrogen bases such as adenine, uracil, cytosine, and guanine.

It is usually double-stranded.

It is usually single-stranded.

It is self-replicating.

It can’t be replicated on its own.

The length of the DNA is quite-large.

The length of RNA is smaller.

There is only one form of DNA that exists in the cell.

There are mainly three forms of the RNA that exist in the cell such as rRNA, tRNA, and mRNA.


Packaging of DNA

In eukaryotes, there is a complex organization of DNA in the chromosome. The negatively charged DNA is wound around the core of histone (positively charged proteins) octamer to form a nucleosome which is the monomeric unit of chromatin.

(image will be uploaded soon)  

Structure of Nucleosome


Central Dogma of Biology

It states that genetic information flows from DNA → RNA → Protein. It was proposed by Francis Crick.

Mechanism of packaging of DNA


DNA-replication

In 1958, Meselson and Stahl experimentally proved that the DNA replicates itself in the semi-conservative manner.

The central dogma of biology

  • The process which involves the duplication of DNA is called DNA replication.

  • It mainly occurs in the S-phase of the cell cycle.

  • The process of DNA replication initiates at Ori(origin of replication).

  • The process of DNA replication is catalyzed by an enzyme named DNA polymerase and the energy for catalyzing it comes from the enzyme Deoxyribonucleoside triphosphate which can also act as the substrate. DNA polymerase always polymerises in the 5'→3’ direction.

  • In the process of replication, two kinds of strands are formed i.e. lagging strand and leading strand.

  • The lagging strand is formed in a discontinuous manner and each fragment is known as Okazaki fragments which are joined together by the enzyme DNA ligase.

Meselson and Stahl experiment


Transcription

The process involves the copying of genetic information from one strand of the DNA into RNA. During this process, only one strand of the DNA gets copied to RNA.


Transcription Unit

 It can be defined by the three regions as mentioned below:

  • Promoter: It is the region where RNA polymerase binds and the process of transcription initiates.

  • The Structural Gene: It is the region between the promoter and the terminator.

  • Terminator: It is the region which marks the end of the transcription process.

DNA replication fork


Transcription in Prokaryotes vs Eukaryotes

Transcription in Prokaryotes

Transcription in Eukaryotes

In prokaryotes, the process of transcription and translation occurs in a  simultaneous manner.

In eukaryotes, the process of transcription and translation occurs separately.

In prokaryotes, the process of transcription occurs in the cytoplasm.

In eukaryotes, the process of transcription and translation occurs in the nucleus and cytoplasm, respectively.

In prokaryotes, there is no need for additional proteins to initiate the process of transcription.

In eukaryotes, additional proteins named as transcriptional factors are required to initiate the process of transcription.

In prokaryotes, RNA polymerase is a complex of 5 polypeptides.

In Eukaryotes, RNA polymerase is a complex of 10-15 polypeptides.

In prokaryotes, there are no post-transcriptional modifications present.

In eukaryotes, the mRNA requires post-transcriptional modifications.


Types of RNAs

rRNA

mRNA

tRNA

It is the component of the ribosome and serves as an organelle of the translation.

It is the kind of RNA that carries a portion of DNA code to the other parts of the cell for further processing.

It is the kind of RNA that transfers a specific amino acid in the cytoplasm to the ribosome.

It is mainly sphere shaped.

It is linear shaped.

It is clover-leaf shaped.

It lacks codon and anticodon sequences.

It consists of codon sequences.

It consists of anticodon sequences.

It accounts approximately 80% of the total RNA present in the cell.

It accounts approximately 5% of the total RNA present in the cell.

It accounts approximately 12-15% of the total RNA present in the cell.


Transcription unit

Genetic Codon

These are the sequence of bases in the mRNA that codes for a particular amino acid in the protein synthesis. It is made up of three nucleotides and is termed as triplets. There are a total of 64 codons, out of which 61 codes for amino acids. The remaining three codons are named as stop codons such as UAA, UAG, and UGA.


Types of RNA


Translation 

The process involves the polymerization of amino acids. During this process, the messenger RNA works together with the transfer RNA i.e. tRNA and ribosome for the synthesis of proteins. The process of translation completes in three steps:

  • Initiation

  • Elonation

  • Termination

Genetic code table


Regulation of Gene Expression

Gene regulation is defined as the process of turning on/off the genes. It ensures that particular genes are expressed at a particular time. It is important for the proper development of the embryo as well as also allows the cells to react quickly to the changes in their environments. In eukaryotes, it can be performed on various levels such as transcriptional level, processing level, transport of mRNA from the nucleus to the cytoplasm, and translational level while in prokaryotes control of gene expression is mainly at the initiation of transcription.


LAC Operon

Operon is defined as the genetic regulatory system found in bacteria and viruses. It was Jacob and Monad who first showed the transcriptionally regulated system in the lac operon.

Mechanism of translation


Human Genome Project

Human genome project was called a mega-project. It was launched in the year of 1990. The main objectives of this project were:

  • Identification of the complete human genome.

  • Development of genome sequence databases to store the data.

  • Transfer related technologies to other sectors, such as industries.

  • Improvement in tools for data analysis.

The human genome project was completed in 2003.


DNA Fingerprinting

DNA fingerprinting is the method of finding out the genetic makeup of any organism. It is also known as DNA profiling, genetic fingerprinting, etc. The procedure involves: 

  • DNA sample collection   

  • Cleavage of DNA into DNA fragments by restriction endonuclease 

  • Separation of DNA fragmentation by electrophoresis  

  • Southern blotting  

  • Autoradiography to obtain the bands 

  • Visualization of DNA fingerprints


The Applications of this Technique are as Follows:

  1. In forensic science, it is used to identify the criminal.

  2. By using this technology, one can map the evolutionary history of an organism and its overall linkage with the other groups.

  3. It is used to identify the biological parents of the respective individual/offspring.

  4. DNA fingerprinting can also be utilized in the field of agriculture. The information about the disease-causing agent can be identified.


Solved Examples From the Chapter

1. Give a reason for the discontinuous synthesis of DNA on one of the parental strands?

Ans: The biological process of DNA synthesis naturally occurs in 5′ to 3′ directions in the double-stranded DNA. During the synthesis of DNA, both the strands act as templates, only one out of two (3′ to 5′ direction) can synthesize the parallel strand in 5’→3′ direction. The other strand (5′ to 3′ direction) is synthesized in the opposite direction producing small stretches of DNA which are known as Okazaki fragments which are joined together by the DNA ligase. Hence, it is because of  this reason that there is the discontinuous synthesis of DNA on one of the parental strands.


2. Sometimes, the young ones born have an extremely different set of eyes or limbs.  Give a relevant explanation for the abnormality.

Ans: This abnormality may be caused due to variety of factors such as alcohol abuse by the mother during her pregnancy, side effects of medicine, environmental factors, such as maternal exposure to the chemicals, radiations, viruses, and it can also occur due to the non-coordination in the regulation of expression in the set of genes that are  associated with the development of the organs.


3. Complete the blanks a, b, c, and d on the basis of the Frederick Griffith Experiment.

    S Strain →→ inject into mice →→ (a)

    R strain →→ inject into mice →→ (b)

    S strain (heat killed) →→ inject into mice →→ (c)

    S strain (heat killed) + R strain (live) →→ inject into mice →→ (d)

Ans:

(a) It will result in the death of the mice.

(b) The mice will live.

(c) The mice will live.

(d) It will result in the death of the mice.

The principle of transformation was given by Griffth. In this experiment, he concluded that in the infected mice, some “transforming principle” gets transferred from heat-killed S-strain of Streptococcus pneumoniae to R-strain and this enables them to make the smooth polysaccharide coat which enables them to become virulent. This may be due to the transfer of the genetic material. However, the biochemical nature of genetic material was unknown. 


Solved Problems of Previous Year Question From the Chapter

1. The final proof for DNA as the genetic material comes from the experiments of ______.

A. Macleod and Avery

B. Griffith

C. Harvey Mcbride

D. Hershey and Chase

Ans: The correct answer will be option ”D”.

Hershey and Chase found that the bacteria which were infected with viruses that had radioactive DNA were radioactive, indicating that DNA was the material that passed from the virus to the bacteria while the bacteria that were infected with viruses that had radioactive proteins were not radioactive, which indicates that proteins did not enter the bacteria from the viruses. Hence, it is the DNA which acts as the genetic material.


2. All of the following are part of an operon except______.

A. structural genes

B. a promoter

C. an enhancer

D. an operator

Ans: The correct answer is option “C”.

Operon is defined as the genetic regulatory system found in bacteria and viruses.

Enhancers are the regulatory sequence of the DNA. Specific proteins through which they are bound are called transcription factors. They enhance the rate of  transcription of target genes. They are not the part of operon.


3. Complete the flowchart on central dogma.

Lac operon model

A. (a) - Replication; (b) -Transcription; (c) - Transduction; (d) - Protein

B. (a) -Translation; (b) - Replication; (c) -Transcription; (d) -Transduction

C. (a) - Replication; (b) - Transcription; (c) - Translation; (d) - Protein

D. (a) - Transduction; (b) - Translation; (c) - Replication; (d) - Protein

Ans: The correct answer is option “C”.

Central dogma states that genetic information flows from DNA → RNA → Protein. It was proposed by Francis Crick.


Practice Questions

1. Three codons on mRNA are not recognised by tRNA what are they? What is the general term used for them and what is their significance in protein synthesis?

Ans: Genetic codes are the sequence of bases in the mRNA that codes for a particular amino acid in the protein synthesis. It is made up of three nucleotides and is termed as triplets. There are a total of 64 codons, out of which 61 codes for amino acids. The remaining three codons are named as stop codons such as UAA, UAG, and UGA. As we know that these three codons are not recognised by any tRNA, hence, they are helpful in the termination of the protein chain during translation.


2. Why is DNA not RNA the genetic material in the majority of organisms?

Ans: The hydroxyl (-OH) group in the nucleotides of RNA is much more reactive and makes RNA labile and easily degradable. Thus, it is the DNA that acts as genetic material in the majority of organisms.


3. Why is it that transcription and translation could be coupled in a prokaryotic cell but not in a eukaryotic cell?

Ans: In prokaryotes, the mRNA synthesized does not require any kind of processing to become active, so the process of transcription and translation occurs simultaneously in the cytosol while in eukaryotes, primary transcript/pre-mRNA contains both exon and intron and is subjected to a process named as splicing where introns are removed or exons are joined in a definite order to form mature mRNA.


4. In the DNA of an animal, the percentage of adenine is 30, then what will be the percentage of guanine?

a) 40

b) 30

c) 20

d) 70

Ans: The correct answer is option “c”.

Chargaff rule states that in DNA there is always equality in quantity between the bases A and T and between the bases G and C (where A is adenine, T is thymine, G is guanine, and C is cytosine). It is based upon the complementary base pairing between nitrogenous bases of two antiparallel strands of a double-stranded DNA molecule.

Given,

Adenine=30%

Thymine=30%(A=T)

G+C=40

x+x=40

2x=40

x=40/2

x=20

Hence, guanine will be 20%.


Conclusion

This article contains all the important information as per the requirement of students who are preparing for the  NEET and can be really helpful for a quick and effective revision. It includes all the important concepts and topics, questions from the previous year's NEET exam, NEET mock test as well as the Biology NCERT. Make sure to try the Practice question on your own to test your knowledge and to get desired outputs. 

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FAQs on NEET Important Chapter - Molecular Basis of Inheritance

FAQ

1. Is the molecular basis of inheritance important for NEET?

Yes, it is important for the NEET exam because it covers most of the important topics and the concepts that are useful for the exam.

2. What are the important topics of the chapter Molecular Basis of Inheritance?

Although it is one of the most important chapters in terms of the NEET exam, some of the important topics from where the questions are asked are the search for genetic material, double-helical structure of DNA, packaging of DNA, the central dogma of biology, replication, transcription, translation, gene regulation:Lac operon, etc.

3. Is NCERT enough for preparing for the NEET exam?

Yes, it is enough. One can score very well by going through it again and again because every time a person receives new information which is very important in terms of exams.