DNA holds genetic information, whereas RNA transfers this genetic information from DNA to ribosomes made of RNA and proteins.
Both deoxyribonucleic and ribonucleic acid are polymers of nucleotides.
Nucleotides consist of pentose which is a 5 carbon sugar, a nitrogen containing organic base and a phosphate group.
The components of a DNA nucleotide are deoxyribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or thymine.
Adenine and guanine both have a double ring structure and are classified as purine bases.
The components of an RNA nucleotide are ribose, a phosphate group and one of the organic bases adenine, cytosine, guanine or uracil.
Thymine, uracil and cytosine all have a single ring structure and are classified as pyrimidines.
Nucleotides join together by phosphodiester bonds formed in condensation reactions.
DNA structure consists of a double helix composed of two polynucleotides joined together by hydrogen bonds between complementary bases.
In DNA, the 2 strands lie antiparallel and complementary base pairing takes place between the 5’ to 3’ strand and the 3’ to 5’ strand.
A purine always joins to a pyrimidine base.
Depending on the bases, a different number of hydrogen bonds are formed.
Adenine and Thymine join together by 2 hydrogen bonds.
Cytosine and guanine join together by 3 hydrogen bonds.
Nucleotides are joined together by phosphodiester bonds.
RNA is a relatively short polynucleotide chain.
An RNA nucleotide consists of ribose instead of deoxyribose, a phosphate group and one of the organic bases adenine, cytosine, guanine and uracil (instead of thymine).
Insertion is when 1 or more nucleotides are inserted into the DNA strand.
Nonsense is a mutation resulting in a stop codon hence no polypeptide chain will be formed.
Missense is a mutation resulting in a different amino acid being coded for hence changing the polypeptide chain.
Mutations are a result of substitution, insertion, and deletion of nucleotides in the DNA strand.
Deletion is when 1 or more nucleotides are deleted in the DNA strand.
Silent is a mutation resulting in a different codon however it still codes for the same amino acid meaning the polypeptide chain produced is the same.
Substitution is when 1 or more nucleotides are substituted by another in the DNA strand.
DNA replication involves the semi-conservative replication of DNA ensuring genetic continuity between generations of cells meaning that genetic information is passed on from one generation from the next.
DNA replication occurs during the S phase of the cell cycle.
The steps of semi-conservative replication of DNA are as following: The double helix unwinds and the hydrogen bonds between the complementary bases break using DNA helicase thus separating the two strands of DNA.
One of the strands is used as the template and complementary base pairing occurs between the template strand and free nucleotides.
Adjacent nucleotides are joined by phosphodiester bonds formed in condensation reactions using DNA polymerase.
DNA polymerase only works in the 5’ to 3’ direction.
This means that DNA polymerase is only able to add nucleotides starting from the 3’ end of the new strand.
The leading strand is replicated continuously in the 3’ to 5’ direction.
The second strand which is called the lagging strand is replicated discontinuously in the 5’ to 3’ direction.
The Okazaki fragments are joined together with DNA ligase.
Proteins are polypeptide chains, coded for by a gene.
In eukaryotic cells, the RNA molecule formed from transcription is called the primary transcript.
There are two stages of protein synthesis: transcription and translation.
mRNA detaches from DNA then moves out of the nucleus through a pore and attaches to a ribosome in the cytoplasm which is the site of next stage of protein synthesis called translation.
A gene mutation occurs when the base sequence of DNA is altered.