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DNA & RNA Structure -------------------------------------------------------------------- cont. lec-4
Comparison DNA RNA
Full Name Deoxyribonucleic Acid Ribonucleic Acid
Function
DNA replicates and stores genetic information. It is
a blueprint for all genetic information contained
within an organism.
RNA converts the genetic information
contained within DNA to a format used to
build proteins, and then moves it to ribosomal
protein factories.
Structure
DNA consists of two strands, arranged in a double
helix. These strands are made up of subunits called
nucleotides. Each nucleotide contains a phosphate, a
5-carbon sugar molecule, and a nitrogenous base.
RNA only has one strand, but like DNA, is
made up of nucleotides. RNA strands are
shorter than DNA strands. RNA sometimes
forms a secondary double helix structure, but
only intermittently.
Length
DNA is a much longer polymer than RNA. A
chromosome, for example, is a single, long DNA
molecule, which would be several centimetres in
length when unravelled.
RNA molecules are variable in length, but
much shorter than long DNA polymers. A
large RNA molecule might only be a few
thousand base pairs long.
Sugar
The sugar in DNA is deoxyribose, which contains
one less hydroxyl group than RNA’s ribose.
RNA contains ribose sugar molecules,
without the hydroxyl modifications of
deoxyribose.
Bases
The bases in DNA are Adenine (‘A’), Thymine
(‘T’), Guanine (‘G’) and Cytosine (‘C’).
RNA shares Adenine (‘A’), Guanine (‘G’)
and Cytosine (‘C’) with DNA, but contains
Uracil (‘U’) rather than Thymine.
Base Pairs
Adenine and Thymine pair (A-T)
Cytosine and Guanine pair (C-G)
Adenine and Uracil pair (A-U)
Cytosine and Guanine pair (C-G)
Location
DNA is found in the nucleus, with a small amount
of DNA also present in mitochondria.
RNA forms in the nucleolus, and then moves
to specialised regions of the cytoplasm
depending on the type of RNA formed.
Reactivity
Due to its deoxyribose sugar, which contains one
less oxygen-containing hydroxyl group, DNA is a
more stable molecule than RNA, which is useful for
RNA, containing a ribose sugar, is more
reactive than DNA and is not stable in
alkaline conditions. RNA’s larger helical
a molecule which has the task of keeping genetic
information safe.
grooves mean it is more easily subject to
attack by enzymes.
Ultraviolet
(UV)
Sensitivity
DNA is vulnerable to damage by ultraviolet light.
RNA is more resistant to damage from UV
light than DNA.
Recombinant DNA technology :
A technique mainly used to change the phenotype of an organism (host) when a genetically altered vector is
introduced and integrated into the genome of the organism. So, basically, this process involves the introduction of a
foreign piece of DNA structure into the genome which contains our gene of interest. This gene which is introduced
is the recombinant gene and the technique is called the recombinant DNA technology.
There are multiple steps, tools and other specific procedures followed in the recombinant DNA technology, which
is used for producing artificial DNA to generate the desired product. Let’s understand each step more in detail.
The enzymes which include the restriction enzymes help to cut, the polymerases- help to synthesize and the ligases-
help to bind. The restriction enzymes used in recombinant DNA technology play a major role in determining the
location at which the desired gene is inserted into the vector genome. They are two types, namely Endonucleases and
Exonucleases.
The Endonucleases cut within the DNA strand whereas the Exonucleases remove the nucleotides from the ends of
the strands. The restriction endonucleases are sequence-specific which are usually palindrome sequences and cut the
DNA at specific points. They scrutinize the length of DNA and make the cut at the specific site called the restriction
site. This gives rise to sticky ends in the sequence. The desired genes and the vectors are cut by the same restriction
enzymes to obtain the complementary sticky notes, thus making the work of the ligases easy to bind the desired gene
to the vector.
The vectors – help in carrying and integrating the desired gene. These form a very important part of the tools of
recombinant DNA technology as they are the ultimate vehicles that carry forward the desired gene into the host
organism. Plasmids and bacteriophages are the most common vectors in recombinant DNA technology that are used
as they have a very high copy number. The vectors are made up of an origin of replication- This is a sequence of
nucleotides from where the replication starts, a selectable marker – constitute genes which show resistance to certain
antibiotics like ampicillin; and cloning sites – the sites recognized by the restriction enzymes where desired DNAs
are inserted.
Host organism – into which the recombinant DNA is introduced. The host is the ultimate tool of recombinant DNA
technology which takes in the vector engineered with the desired DNA with the help of the enzymes.

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DNA & RNA structure.pdf

  • 1. DNA & RNA Structure -------------------------------------------------------------------- cont. lec-4 Comparison DNA RNA Full Name Deoxyribonucleic Acid Ribonucleic Acid Function DNA replicates and stores genetic information. It is a blueprint for all genetic information contained within an organism. RNA converts the genetic information contained within DNA to a format used to build proteins, and then moves it to ribosomal protein factories. Structure DNA consists of two strands, arranged in a double helix. These strands are made up of subunits called nucleotides. Each nucleotide contains a phosphate, a 5-carbon sugar molecule, and a nitrogenous base. RNA only has one strand, but like DNA, is made up of nucleotides. RNA strands are shorter than DNA strands. RNA sometimes forms a secondary double helix structure, but only intermittently. Length DNA is a much longer polymer than RNA. A chromosome, for example, is a single, long DNA molecule, which would be several centimetres in length when unravelled. RNA molecules are variable in length, but much shorter than long DNA polymers. A large RNA molecule might only be a few thousand base pairs long. Sugar The sugar in DNA is deoxyribose, which contains one less hydroxyl group than RNA’s ribose. RNA contains ribose sugar molecules, without the hydroxyl modifications of deoxyribose. Bases The bases in DNA are Adenine (‘A’), Thymine (‘T’), Guanine (‘G’) and Cytosine (‘C’). RNA shares Adenine (‘A’), Guanine (‘G’) and Cytosine (‘C’) with DNA, but contains Uracil (‘U’) rather than Thymine. Base Pairs Adenine and Thymine pair (A-T) Cytosine and Guanine pair (C-G) Adenine and Uracil pair (A-U) Cytosine and Guanine pair (C-G) Location DNA is found in the nucleus, with a small amount of DNA also present in mitochondria. RNA forms in the nucleolus, and then moves to specialised regions of the cytoplasm depending on the type of RNA formed. Reactivity Due to its deoxyribose sugar, which contains one less oxygen-containing hydroxyl group, DNA is a more stable molecule than RNA, which is useful for RNA, containing a ribose sugar, is more reactive than DNA and is not stable in alkaline conditions. RNA’s larger helical
  • 2. a molecule which has the task of keeping genetic information safe. grooves mean it is more easily subject to attack by enzymes. Ultraviolet (UV) Sensitivity DNA is vulnerable to damage by ultraviolet light. RNA is more resistant to damage from UV light than DNA. Recombinant DNA technology : A technique mainly used to change the phenotype of an organism (host) when a genetically altered vector is introduced and integrated into the genome of the organism. So, basically, this process involves the introduction of a foreign piece of DNA structure into the genome which contains our gene of interest. This gene which is introduced is the recombinant gene and the technique is called the recombinant DNA technology. There are multiple steps, tools and other specific procedures followed in the recombinant DNA technology, which is used for producing artificial DNA to generate the desired product. Let’s understand each step more in detail. The enzymes which include the restriction enzymes help to cut, the polymerases- help to synthesize and the ligases- help to bind. The restriction enzymes used in recombinant DNA technology play a major role in determining the location at which the desired gene is inserted into the vector genome. They are two types, namely Endonucleases and Exonucleases. The Endonucleases cut within the DNA strand whereas the Exonucleases remove the nucleotides from the ends of the strands. The restriction endonucleases are sequence-specific which are usually palindrome sequences and cut the DNA at specific points. They scrutinize the length of DNA and make the cut at the specific site called the restriction site. This gives rise to sticky ends in the sequence. The desired genes and the vectors are cut by the same restriction enzymes to obtain the complementary sticky notes, thus making the work of the ligases easy to bind the desired gene to the vector. The vectors – help in carrying and integrating the desired gene. These form a very important part of the tools of recombinant DNA technology as they are the ultimate vehicles that carry forward the desired gene into the host organism. Plasmids and bacteriophages are the most common vectors in recombinant DNA technology that are used as they have a very high copy number. The vectors are made up of an origin of replication- This is a sequence of nucleotides from where the replication starts, a selectable marker – constitute genes which show resistance to certain antibiotics like ampicillin; and cloning sites – the sites recognized by the restriction enzymes where desired DNAs are inserted. Host organism – into which the recombinant DNA is introduced. The host is the ultimate tool of recombinant DNA technology which takes in the vector engineered with the desired DNA with the help of the enzymes.