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DNA (deoxyribonucleic acid) is double helical structure that was cracked by Watson and Crick based on the X-ray
crystallography results. Each strand of a DNA helix is composed of repeating units of nucleotides. Nucleotide consists of 3
components: ribose or deoxyribose sugar, nitrogenous base (purines or pyrimidines) and phosphate.
There are two types of purines- adenine and guanine. Pyrimidines are of three types- thymine, cytosine, and uracil. All
nucleotides are common in DNA and RNA. But uracil is found in RNA and thymine is present only in DNA. DNA is negatively
charged due to the presence of negatively charged phosphate groups. A nitrogenous base is linked to the pentose sugar
through the N-glycosidic linkage. Two nucleotides are linked through 3'-5' phosphodiester linkage to form a dinucleotide.
A polymer formed in such a manner has a free phosphate group at 5'-end of ribose sugar, which is referred to as 5’-end
of polynucleotide chain. The other end of the polymer has a free 3'-OH group of the ribose sugar. This is referred to as 3'-
end of the polynucleotide chain. The bonding between sugar and phosphates forms the backbone of a polynucleotide
chain. The nitrogenous bases are linked to sugar moiety and project from the backbone.
The salient feature of the double helix structure of DNA are as follows-
• Two polynucleotides chains wrap around each other, where the backbone is constituted by sugar-phosphate, and
bases project inside.
• The two DNA chains are antiparallel to each other. It means, if one chain has the polarity 5'-3', the other has 3'-5'.
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Study Materials
NCERT Solutions for Class 6 to 12 (Math & Science)
Revision Notes for Class 6 to 12 (Math & Science)
RD Sharma Solutions for Class 6 to 12 Mathematics
RS Aggarwal Solutions for Class 6, 7 & 10 Mathematics
Important Questions for Class 6 to 12 (Math & Science)
CBSE Sample Papers for Class 9, 10 & 12 (Math &
Science)
Important Formula for Class 6 to 12 Math
CBSE Syllabus for Class 6 to 12
Lakhmir Singh Solutions for Class 9 & 10
Previous Year Question Paper
CBSE Class 12 Previous Year Question Paper
CBSE Class 10 Previous Year Question Paper
JEE Main & Advanced Question Paper
NEET Previous Year Question Paper
Positively charged basic proteins that surround the DNA is known as histones. Histones are rich in basic amino acids such
as lysine and arginine. Histones are organized to form a unit of eight molecules called as histone octamer. The DNA is
negatively charged and is packaged by wrapping around the positively charged histone octamer. This forms a structure
called nucleosome. A nucleosome typically contains 200 base pairs of DNA helix. Nucleosomes form the repeating unit of
a structure called chromatin in nucleus. Chromatin are thread-like stained bodies seen in nucleus. The nucleosomes in
chromatin appear as ‘beads-on-string’ structure when viewed under electron microscope (EM). The beads-on-string
structure in chromatin is packaged to form chromatin fibers that are further coiled and condensed at metaphase stage of
cell division to form chromosomes. At higher levels chromatin packaging requires additional proteins. These proteins are
the Non-Histone Chromosomal (NHC) proteins. In a typical nucleus, loosely packed region of chromatin stains light and
are referred to as euchromatin. The densely chromatin stains dark are called as Heterochromatin. Euchromatin is said to
be transcriptionally active chromatin, whereas heterochromatin is inactive.
Griffith performed an experiment known as transforming experiment. He used two strains of Pneumococcus. These two
different strains were used to infect the mice. The two strains used were type III-S (smooth), that contains outer capsule
made up of polysaccharide and type II-R (rough) strain do not contain capsule. The capsule protects the bacteria from the
host immune system.
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Fig.3. Griffith experiment
This proves that there is some transforming substance present in heat killed S strain that is converting or transforming the
rough strain into virulent strain that is responsible for the death of the mouse. This transforming substance is was later
found to be DNA.
Alfred Hershey and Martha Chase (1952) performed an experiment to prove that DNA is the genetic material. They worked
on bacteriophages, which are viruses that infects the bacteria. When the bacteriophage attaches to the bacteria, its
genetic material enters into the bacterial cell. The viral genetic material uses the bacterial cell to synthesize more viral
particles. Hershey and Chase grew some viruses on a medium that contained radioactive phosphorus and other medium
that contained radioactive sulfur. When radioactive phosphorus was present in the medium the viruses contained
radioactive DNA but not radioactive protein. This is because DNA contains phosphorus, but protein does not. Similarly,
when the growth medium contained radioactive sulfur the viruses contained radioactive protein but not radioactive DNA.
This is because DNA does not contain sulfur.
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Fig.4. Hershey and chase experiment
Those bacteria were found to be radioactive only when they were infected with viruses that had radioactive DNA. This
indicates that DNA was the material that passed from the virus to the bacteria. Bacteria infected with viruses containing
radioactive proteins were not radioactive. This indicates that proteins did not enter the bacteria from the viruses. DNA is
therefore the genetic material that is passed from virus to bacteria. This experiment proves that DNA is the genetic
material.
It is an explanation about how the flow of genetic information occurs in a biological system. This explains how DNA
replicates and then gets converted into messenger RNA (mRNA) via transcription. Then this mRNA is translated to form
proteins.
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DNA replication
DNA replication is a process of producing two identical copies of DNA from a single DNA molecule. It is a process of
biological inheritance. DNA is a double helix in which two strands are complementary to each other. These two strands of
a helix separate at the time of replication to form two new DNA molecules. Out of the two strands of DNA formed, one is
identical to one of the strand and another strand is complementary to the parent strand. This form of replication is known
as semi-conservative replication. Before the cell enters the mitosis, the DNA is replicated in S phase of interphase. DNA
polymerase in the most important enzyme involved in DNA replication. DNA replication is an energy dependent process.
During the process of replication, the two DNA strands does not separate completely, the replication occur within the
small opening of the DNA helix known as replication fork. The DNA polymerase catalyze the reaction in 5’ to 3’.
Consequently, on one strand (the template with polarity 3'-5'), the replication is continuous, while on the other (the
template with polarity 5'-3'), it is discontinuous. The enzyme DNA ligase later joins the discontinuously synthesized
fragments. The strand which is synthesized continuously is known as leading strand whereas the one synthesized
discontinuously is known as lagging strand. Replication begins on the specific site on the DNA, known as origin of
replication.
Transcription
It is a process of formation of RNA such as messenger RNA from DNA before gene expression or protein synthesis occurs.
During transcription, one of the strand of DNA acts as template for mRNA formation. The synthesis of mRNA occurs via
RNA polymerase enzyme. Transcription usually occurs for a particular DNA segment which is required further for gene
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expression. Other than the messenger RNA, other forms of RNA such as ribosomal RNA, micro RNA, small nuclear RNA can
also be transcribed in the similar manner. A transcription unit in DNA consists of following three regions- a promoter,
structural gene and a terminator. DNA dependent RNA polymerase catalyzes the polymerization in 5’-3’ direction.
Promoter is the region where RNA polymerase binds. Terminator defines the end of transcription.
Initiation involves the binding of the RNA polymerase to promoter. Single type of DNA dependent RNA polymerase
catalyzes the transcription of all types of RNA in bacteria.
Termination factor helps in termination of transcription. The RNA synthesized after transcription is known as primary
transcript. The primary transcript undergoes modification such as splicing, capping, tailing etc. Primary transcript consist
of introns and exons. The removal of introns is known as splicing. Addition of poly-A tail at the 3’-end of the RNA is known
as tailing. In capping an unusual nucleotide (methyl guanosine triphosphate) is added to the 5'-end of RNA.
Some viruses have a property of reverse transcription. They are able to convert RNA template into DNA. The enzyme used
is known as reverse transcriptase.
Translation
This is the process of gene expression or protein synthesis that occurs in cytosol. Ribosomes are the cell organelles that
are involved in protein synthesis. The messenger RNA formed by the process of transcription is decoded by ribosomes to
form a polypeptide made up of amino acids. Messenger RNA is composed of polymer of nucleotides or codon. Each codon
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consists of 3 nucleotides that will code for a single amino acid. There are some important components that are involved
in protein synthesis- ribosomes, messenger RNA and transfer RNA (tRNA).
Transfer RNA is involved in physically linking mRNA and the amino acid sequence of proteins.
Genetic code
The set of rules by which information encoded in genetic material is translated into proteins in the living cells. Salient
features of genetic code are as follows-
• The codon consists of three nucleotides. 61 codons code for 20 different amino acids.
• One codon codes for one amino acid.
• One amino acid can be coded by more than one codon.
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Fig.9. Genetic code
All the genes in the living cells is not active all the time. They become active when needed. Expression is controlled by
genes are known as regulatory genes. Regulation in eukaryotes can occur at the following levels-
• Transcriptional level.
• Processing level.
• Transport of mRNA from nucleus to the cytoplasm.
• Translational level.
An operon consists of structural genes, operator genes, promoter genes, promoter genes, regulator genes, and repressor.
Lac operon consist of lac Z, lac Y and lac A genes. Lac Z codes for galactosidase, lac Y codes for permease and lac A codes
for transacetylase. When repressor molecules bind the operator, genes are not transcribed. When repressor does not bind
the operator and instead inducer binds, transcription is switched on. In case of lac operon, lactose is an inducer. So, binding
of lactose to operator, switch on the transcription.
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Fig.10. Lactose operon
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