πΈ Chapter 5
Molecular Basis Of Inheritance
𧬠1. Introduction
Every living organism passes its traits from one generation
to the next. This transmission of genetic information is controlled by DNA
— the molecule of inheritance.
This chapter explains the structure of DNA, replication, transcription,
translation, genetic code, gene expression regulation, Human Genome Project and DNA Fingerprinting.
π§« 2. The DNA
DNA is a long polymer of deoxyribonucleotides.The length of DNA is usually defined as the number ofnucleotides(or a pair of nucleotide referred to as base pairs) present in it .This is also the characteristic of an organism.
Discovery
- Friedrich Miescher (1869) discovered a substance called nuclein
(now known as DNA) from pus cells.
- Later, DNA was found to be the genetic
material in most organisms (except some viruses which have RNA).
π§© 3. Chemical Structure of Polycucleotide Chain(DNA/RNA):
Both DNA and RNA are polynucleotides,
i.e., chains of repeating units called nucleotides.
Each Nucleotide has 3 components:
1.
Nitrogenous
base
o Purines: Adenine (A), Guanine (G)
o Pyrimidines: Cytosine (C), Thymine (T in DNA) or
Uracil (U in RNA)
2.
Pentose
sugar
o Deoxyribose in DNA
o Ribose in RNA
3.
Phosphate
group
Nitrogenous bases:
There are two types of nitrogenous bases-Purines(Adenine and Guanine), and
Pyrimidines(Cytosine,Uracil and Thymine)
Cytosine is common for both DNA and RNA and Thymine is present in DNA .Uracil is present in RNA.
A nitrogenous base is linked to the OH of 1`C pentose sugar through a N-glycosidic linkage to form a nucleoside, such as adenosine or deoxyadenosine , guanosine or deoxyguanosine.
When a phosphate group is linked to OH of 5`C of a nucleoside through phosphoester linkage.a corresponding nucleotide is formed.
Two nucleotides are linked through 3`-5` phosphodiester linkage to form a dinucleotide.
More nucleotides can be joined in such a manner to form a polynucleotide chain.
A polymer thus formed has at one end a free phosphate moiety at 5` -end of sugar, which is referred to as 5`-end of polynucleotide chain.
Similarly , at the other end of the polymer the sugar has a free OH of 3`C group which is referred to as 3`-end of polynucleotide chain.
The backbone of a polynucleotide chain is formed due to sugar and phospahtes.
The nitrogenous bases linked to sugar moiety project from the backbone.
⚛️ 4. Structure of DNA (Watson and
Crick Model – 1953)
Main Features:
- DNA is a double-stranded
helical structure.
- Each strand is made of polynucleotide
chains.
- The two strands are complementary
and antiparallel.
- The strands are held by hydrogen
bonds between nitrogenous bases:
- A pairs with T (via 2 H-bonds)
- G pairs with C (via 3 H-bonds)
- Sugar-phosphate backbone lies on the outside; bases
face inward.
- Pitch of helix: 3.4 nm
- Distance between two bases: 0.34 nm
- Number of base pairs per turn: 10
π§ NEET Tip: The total length of DNA in a
human cell = 2.2 meters (approx).
π§ͺ 5. Types of DNA
|
Type |
Strands |
Base pairs/turn |
Helix |
Found in |
|
A-DNA |
Double |
11 |
Right-handed |
Dehydrated condition |
|
B-DNA |
Double |
10 |
Right-handed |
Most common form |
|
Z-DNA |
Double |
12 |
Left-handed |
Rich in GC pairs |
𧬠6. Packaging of DNA
Since the DNA length (~2.2 m) is much longer than the cell
nucleus (~6 ΞΌm), it must be packaged compactly.
In Prokaryotes (Bacteria):
- DNA is circular and naked,
not associated with histones.
- Forms a nucleoid region
attached to proteins.
In Eukaryotes:
- DNA is complexed with positively
charged histone proteins to form nucleosomes.
- Each nucleosome = DNA + 8
histone proteins (H2A, H2B, H3, H4 ×2 each)
→ Held by linker DNA (~200 bp).
These nucleosomes coil further to form chromatin →
condense into chromosomes during cell division.
π 7. The Search for Genetic
Material
Griffith’s Experiment (1928)
- Worked on Streptococcus
pneumoniae (R and S strains).
- Observation: Heat-killed S strain + live R
strain → killed mice.
- Concluded: Some transforming
principle converted R → S type.
Avery, MacLeod & McCarty (1944)
- Treated the transforming
substance with enzymes that destroy DNA, RNA, or proteins.
- Only when DNA was destroyed,
transformation didn’t occur → DNA is the transforming principle.
Hershey & Chase Experiment
(1952)
- Used bacteriophage (T2
virus) with radioactive Sulphur (³⁵S) and Phosphorus (³²P).
- ³²P-labeled DNA entered
bacteria → proved DNA is genetic material.
𧬠8. RNA World
- RNA was the first genetic
material (can store information + catalyze reactions).
- DNA evolved later — more stable
and suitable for long-term storage.
π§ NEET Tip: RNA acts as both genetic
material (in some viruses) and catalyst (e.g., ribozymes).
π 9. Replication of DNA
(Semi-conservative Model)
Meselson and Stahl Experiment (1958)
- Used E. coli with heavy
nitrogen (¹⁵N) and light nitrogen (¹⁴N).
- After one generation in ¹⁴N,
DNA was intermediate → proved semi-conservative replication.
Process of DNA Replication
1.
Initiation:
o DNA unwinds by helicase enzyme,
forming a replication fork.
2.
Elongation:
o DNA polymerase adds nucleotides only in 5′ → 3′
direction.
o Leading strand synthesized continuously.
o Lagging strand synthesized in short fragments
(Okazaki fragments).
3.
Termination:
o Fragments joined by DNA ligase.
π§ NEET Tip:
- DNA polymerase III is the main enzyme in
prokaryotes.
- Requires primer (RNA) to
start synthesis.
𧬠10. Transcription (DNA →
RNA)
Enzyme: RNA Polymerase
Steps:
1.
Initiation: RNA polymerase binds to promoter
region.
2.
Elongation: RNA chain grows complementary to
DNA template.
3.
Termination: RNA polymerase detaches at the terminator
sequence.
In Eukaryotes:
- 3 types of RNA polymerases:
- RNA pol I: rRNA
- RNA pol II: mRNA
- RNA pol III: tRNA, snRNA
π§ Post-transcriptional Modifications (in
eukaryotes):
- Addition of 5′ cap
(methyl guanosine triphosphate)
- Poly-A tail at 3′ end
- Splicing (removal of introns)
π‘ 11. Genetic Code
Features:
- Triplet code: 3 bases = 1 codon → 1 amino
acid.
- Degenerate: One amino acid may have
multiple codons.
- Unambiguous: Each codon specifies only one
amino acid.
- Universal: Same code in all organisms.
- Start codon: AUG (Methionine)
- Stop codons: UAA, UAG, UGA
π§ NEET Tip: 64 possible codons; 61 code for
amino acids, 3 are stop codons.
⚙️ 12. Translation (Protein
Synthesis)
Steps:
1.
Activation: Amino acids attach to tRNA
(charging).
2.
Initiation: Ribosome binds to mRNA at start
codon (AUG).
3.
Elongation: Peptide bonds form between amino
acids.
4.
Termination: Stop codon signals release of
polypeptide.
Key Molecules:
- mRNA: Carries codon sequence.
- tRNA: Brings amino acid (anticodon
complementary to codon).
- rRNA: Catalytic part of ribosome.
π¬ 13. Regulation of Gene
Expression
Lac Operon Model (in E. coli)
- Proposed by Jacob and Monod
(1961).
Components:
1.
Structural
genes (Z, Y, A)
→ Enzymes for lactose metabolism.
2.
Promoter
(P) → Binding site for RNA polymerase.
3.
Operator
(O) → Binding site for repressor.
4.
Regulator
gene (i) →
Produces repressor protein.
Working:
- In absence of lactose →
Repressor binds to operator → Transcription OFF.
- In presence of lactose →
Repressor inactivated → Transcription ON.
π§ NEET Tip: The lac operon is an example of inducible
operon.
𧬠14. Human Genome Project
(HGP)
Goals:
- Identify all human genes
(~20,000–25,000).
- Determine entire base sequence
(3 billion bp).
- Store data for research.
Results:
- Less than 2% DNA codes for
proteins.
- Repetitive sequences found in
large amount.
- Genes are unevenly distributed.
π§« 15. DNA Fingerprinting
Principle:
- Based on polymorphism in DNA
sequence.
- Uses VNTRs (Variable Number
Tandem Repeats).
Steps:
1.
DNA
extraction
2.
Restriction
enzyme digestion
3.
Gel
electrophoresis
4.
Southern
blotting
5.
Hybridization
with radioactive probes
6.
Autoradiography
Uses:
- Paternity testing
- Criminal identification
- Evolutionary studies
π§ Scientist: A. J. Jeffreys (1985)
π 16. Important Definitions
|
Term |
Definition |
|
Gene |
Functional unit of inheritance |
|
Genome |
Total genetic material in an organism |
|
Transcriptome |
All RNA molecules transcribed from genome |
|
Mutation |
Sudden change in DNA sequence |
|
Exon |
Coding region of a gene |
|
Intron |
Non-coding region removed during splicing |
π§ 17. Key Diagrams (from
NCERT)
1.
Watson–Crick
Model of DNA
2.
Packaging
of DNA (Nucleosome structure)
3.
Semi-conservative
replication
4.
Transcription
unit
5.
Lac
Operon model
(In class, practice labeling these diagrams perfectly;
they are often asked for 3–5 marks.)
π― 18. Important NCERT
Keywords
- Polynucleotide chain
- Nucleosome
- Replication fork
- Okazaki fragment
- Promoter, Operator, Repressor
- Semi-conservative
- Genetic code
- Operon
- Polymorphism
- VNTRs
π§© 19. High-Yield Topics for
NEET & Boards
✅ Hershey & Chase Experiment
✅ DNA Packaging
✅ Meselson–Stahl Experiment
✅ Central Dogma
✅ Transcription & Translation
✅ Genetic Code (Properties + Exceptions)
✅ Lac Operon
✅ DNA Fingerprinting
✅ RNA World Hypothesis
π§Ύ 20. Summary (Quick
Revision Sheet)
- DNA → genetic material in most
organisms.
- Double helix: A–T (2 H bonds),
G–C (3 H bonds).
- Replication: Semi-conservative,
5′→3′ direction.
- Transcription → RNA; Translation
→ Protein.
- Genetic code → Triplet,
universal, degenerate.
- Lac operon → Gene regulation
model.
- HGP → Mapped entire human
genome.
- DNA fingerprinting → Based on
VNTR polymorphism.


