Watson and Crick determined DNA structure is a double helix of nucleotides with bases that pair together. DNA is replicated through a semi-conservative process where each old strand acts as a template for a new complementary strand. Errors during replication can lead to mutations in the DNA sequence. During protein synthesis, the DNA code is transcribed into mRNA which is then translated by ribosomes into a polypeptide chain according to the base sequence of codons.
Mitochondrial Inheritance
Apart from the nucleus DNA is also found within another cellular organelle, the mitochondrion.
Each mitochondrion contains multiple copies of a double-stranded, circular DNA molecule of 16,569 base pairs.
This DNA has 37 genes out of which encodes 13 peptides that are subunits of proteins required for oxidative phosphorylation.
There is a complete set of 22 transfer RNAs and two ribosomal RNAs.
Mitochondrial Inheritance
Apart from the nucleus DNA is also found within another cellular organelle, the mitochondrion.
Each mitochondrion contains multiple copies of a double-stranded, circular DNA molecule of 16,569 base pairs.
This DNA has 37 genes out of which encodes 13 peptides that are subunits of proteins required for oxidative phosphorylation.
There is a complete set of 22 transfer RNAs and two ribosomal RNAs.
Molecular evolution, four class of chromosomal mutation, Negative Selection and Positive Selection, Mutations in DNA and protein, Neutral Theory of Molecular Evolution, Evidence supporting neutral evolution, Phylogenetic trees, Methods of Tree reconstruction
A complementation test (sometimes called a "cis-trans" test) can be used to test whether the mutations in two strains are in different genes. By taking an example of Benzer's work, complementation has been explained.
Molecular evolution, four class of chromosomal mutation, Negative Selection and Positive Selection, Mutations in DNA and protein, Neutral Theory of Molecular Evolution, Evidence supporting neutral evolution, Phylogenetic trees, Methods of Tree reconstruction
A complementation test (sometimes called a "cis-trans" test) can be used to test whether the mutations in two strains are in different genes. By taking an example of Benzer's work, complementation has been explained.
Genetic information, stored in the chromosomes and transmitted to daughter cells through DNA replication, is expressed through transcription to RNA and translation into proteins (polypeptide chains). The pathway of protein synthesis is called translation because the “language” of the nucleotide sequence on the mRNA is translated into the “language” of an amino acid sequence. The process of translation requires a genetic code, through which the information contained in the nucleic acid sequence is expressed to produce a specific sequence of amino acids. Any alteration in the nucleic acid sequence may result in an incorrect amino acid being inserted into the polypeptide chain, potentially causing disease or even death of the organism.
Genetic Codon The Three nucleotide base sequence in mRNA that act as code words for amino acids in protein constitute the genetic code or codons.
There are 64 different combinations of three base codons composed of Adenine (A), Guanine (G), Cytosine (C) and Uracil (U).
Written from the 5-’ end to 3’ end.
UAA,UAG & UGA do not code for amino acid. They are called as stop codon or non sense codon.
Characteristics of Genetic Code are:
University: same codon for same amino acid in all living organism.
Specificity: A particular codon will code for the same amino acid,highly specific or unambiguous.
Non overlapping : read from a fixed point as a continuous base sequence.
Degenerate: Most of the amino acids have more than one codon. 61 codons available to code for only 20 amino acids.
DNA :DNA stands for Deoxy Ribonucleic acid.
It’s the genetic code that determines all the characteristics of living organism.
DNA is a double stranded molecule, made up of two chains of nucleotides. Nucleotides consist of three subunits : a sugar, a phosphate group and a nitrogen base pair.
Sugar present is Deoxyribose and Nitrogen bases are :
Adenine (A)
Guanine (G)
Cytosine (C)
Thymine (T)
Structure of DNA : Double helical structure of DNA was proposed by James Watson and Francis Crick in 1953.
Features of model of DNA are:
DNA is a right handed double helix, have two polydeoxyribonucleotide chains twisted around each other on a common axis.
Two strands are antiparallel i.e., one strand runs in the 5’ to 3’ direction while the other in 3’ to 5’ direction.
The diameter of helix is 20 A° (2nm).
Each turn of the helix is 34 A° (3.4 nm) with 10 pairs of nucleotides, each pair placed at a distance of about 3.4 A°.
The two strands are held together by Hydrogen bonds formed by complementary base pairs. The A-T pair has 2 hydrogen bonds while G-C pair has 3 hydrogen bonds.
The complementary base pairing in DNA helix proves Chargaff’s rule. The content of adenine equals to that of thymine (A=T) and guanine equals to that of the cytosine (G≡C).
Function of DNA
RNA
DNA replication
Transcription
Translation
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2. DNA Structure
Watson and Crick determined that DNA is a polymer
of nucleotides arranged in adouble helix. Each
nucleotide is composed of a phosphate group, a
sugar (deoxyribose), and a base. There are a total of
four bases: adenine, thymine,cytosine, and guanine.
Adenine and guanine are purines while cytosine and
thymine are pyrimidines. Base-pairing occurs
between adenine and thymine and between guanine
and cytosine.
3. Additionally, a strand of
DNA has a 5' end and
a 3' end (determined by the
attachment of the
phosphate to deoxyribose).
In the double helix, each
strand of DNA
runs antiparallel (in the
opposite direction) to the
other so that the 5' end on
one strand is across from
the 3' end of the other.
4. RNA Structure
RNA is a polymer of
nucleotides. Unlike DNA,
however, RNA is single-
stranded. Also, the
base thymine is replaced
by the base uracil and the
sugar ribose is used
instead of deoxyribose.
5. There are three kinds of RNA.
Messenger RNA (mRNA) carries a copy of the
DNA code to theribosomes during protein sythesis.
Transfer RNA (tRNA) transports amino acids
(used to form proteins) to their proper place on the
mRNA template.
Ribosomal RNA (rRNA) are the building blocks
of ribosomes. They are created in the nucleolus.
6. DNA Replication
Promoter proteins are produced and bind to DNA at
several sites.
Helicases attach to promoter proteins and break
the hydrogen bondslinking the bases together to open the
helix up.
RNA polymerase reads the exposed nucleotides and
produces an RNA primer (approximately 10
nucleotides in length).
DNA polymerase replicates the DNA (base-pairing)
forming the new strand in the 5' to 3' direction.
7. Because DNA polymerase only reads in the 3' to 5'
direction, and forms the new strand in the opposite
direction, there is a directional problem. Therefore one
molecule of DNA produces a continuous leading
strand in one direction. On the lagging strand, new
primers have to form at many sites and the DNA is
broken up into many small fragments called Okazaki
fragments.
The process of DNA replication occurs at many sites,
called replication bubbles, along the entire DNA
strand.
8. When DNA polymerase reaches the 5' end of the RNA
primer, it is released and other enzymes remove the RNA
primers and replace them with the proper nucleotides.
DNA ligase joins together all of the large leading
fragments and the many small Okazaki fragments.
DNA polymerase also checks and corrects any mistakes
in base pairing.
Topoisomerases prevent kinks as the parent DNA is
unzipped.
9.
10. Mutation
Mistakes in base-pairing are corrected by DNA
polymerase and other mismatch repair enzymes.
Radiation and various reactive chemicals can
cause thymine dimers where
adjacent nucleotides bind to each other instead of to
the complimentary strand. Such errors are usually
fixed by splicing out the affected nucleotides and
replacing them (excision repair).
11. A mutation is a DNA
error that is not repaired.
Some mutations include
using an incorrect
nucleotide (substitution),
deleting a nucleotide
(deletion), and adding a
nucleotide (insertion).
When insertion occurs, all
the subsequent nucleotides
are misplaced causing
a frameshift mutation.
12. Protein Synthesis
Protein synthesis is divided into two phases:
transcription and translation.
In transcription, RNA polymerase unzips DNA
and reads it in the 3' to 5' direction. Free RNA
nucleotides are base paired with the exposed DNA
nucleotides and assembled into mRNA. The mRNA
then leaves the nucleus and moves to the ribosomes
in the cytoplasm. Transcription ends and translation
begins.
13. Translation has four stages.
1. In the amino acid 2. In the initiation
activation stage the ribosome
stage amino acids are moves along the mRNA
attached to the strand until it reaches
appropriate tRNA mole the code for formyl
cules. A molecule of methione (AUG).
ATP is used to activate
the tRNA.
14. 3. In the elongation 4. In the termination
stage the tRNA matches stage a nonsense code is
its anti-codon (three reached and the protein is
nucleotides) with the released.
mRNA codon (three
nucleotides). The amino
acid on the previous tRNA
is transferred to the newly
arrived tRNA and the
empty tRNA leaves. This is
repeated over and over as
the ribosome moves along
the mRNA strand.