The base Pairings in DNA are adenine (A) with thymine (T) and guanine (G) and cytosine (C).
The RNA bases are Adenine (A) with Uracil (U) and Guanine (G) with Cytosine (C) (It can also be Thymine (T) with Adenine (A))
There are three types of RNA: mRNA (messenger), tRNA (transfer) and rRNA (Ribosomal).
RNA nucleotide has a structure of a phosphate group, a nitrogenous group and a ribose sugar (Pentose sugar)
DNA nucleotide has a structure of one phosphate group, a nitrogenous base and a Deoxyribose sugar (Pentose sugar)
DNA has two strands and has many millions of nucleotides in a chain
mRNA is single stranded and has several hundreds of thousands of nucleotides in a chain
tRNA is single stranded and has about 75 nucleotides in a chain
mRNA is a copy of a single gene of the DNA template strand
tRNA has a sugarphosphate backbone
tRNA has a cloverleaf structure and has regions where it is double stranded and regions where it is single stranded.It also has an amino acid attachment site and an anticodon.
Protein synthesis involves two processes transcription and translation
Transcription is the copying of the base sequence of a gene in DNA onto the base sequence of a molecule of mRNA
Translation is the conversion of the base sequence of mRNA into the amino acid sequence of a polypeptide chain.
Transcription occurs in the nucleus of eukaryotic cells.
The base sequence of a gene in DNA contains both introns and exon.
Introns are non-coding intervening sequences within genes on DNA
Exons are coding sequences of DNA
The molecule formed during transcription is called pre-RNA
Post-transcription mRNA has all of the intron sequences removed and the exons are all joined together
The Enzyme DNA Helicase attaches to and unwinds the DNA double helix during transcription.
transcription is when DNA is split in half one strand is used as the template
Splicing is the separation of exons and introns
Translation occurs in the cytoplasm (or anywhere there are ribosomes).
Messenger RNA (mRNA) leaves the nucleus via the nuclear pores in the nuclear membrane and attaches to a ribisome.
In Translation tRNA carrying a specific amino acid binds to the first codon on mRNA via base paring with its anticodon.
Enzymes join amino acids together forming peptide bonds (this requires ATP) and then it moves on to the next codon (triple base)
Many ribosomes can translate a molecule of mENA at the same time (so many polynucleotides can be synthesised at once)
Protein synthesis requires energy / ATP
A gene mutation is a change in the sequence of base pairs in a DNA molecule that may result in an altered polypeptide
The DNA base sequence determines the sequence of amino acids that make up a protein.
There are three ways in which mutations occur: substitution, deletion or insertion
Insertion of nucleotides is when a nucleotide with a new base is randomly inserted into DNA (and is known as an insertion mutation)
Deletion of nucleotides is when a nucleotide and therefore its base is randomly deleted from the DNA sequence.
Substitution of nucleotides is when a base of a nucleotide is randomly swapped for a different base (unlike deletion and insertion substitution only change the amino acid for the triplet base/codon)
Missense mutations is when the mutation alters a single amino acid in the polypeptide chain (EG: sickle cell anemia)
Nonsense mutations is when the mutation creates a premature stop codon (signalling for the cell to stop translation of the mRNA molecule into an amino acid sequence)
Mutations occur spontaneously during DNA replication and are random events that cause permanent changes to the DNA.