A section of DNA that contains a code for making a polypeptide and functional RNA the code is a specific sequence of bases
Polypeptides make proteins and so genes determine the proteins of an organisms
The location of a particular gene on a chromosome is called the locus
Allele
An allele is one of a number of alternative forms of a gene most genes occur in 2 occasionally more, different formed
Chromosomes
In a eukaryotic cell nucleus, DNA is stored as chromosomes
Humans have 23 pairs of chromosomes, 46 in total
Pairs or matching chromosomes are called homologous pairs
A homologous air of chromosomes are exactly the same size have exactly the same genes but might have different alleles
DNA storage in a eukaryotic
DNA is stored as chromosomes inside of the nucleus
Chromosomes in eukaryotic cells are linear in shape
To tightly coil the DNA to fit in the nucleus as chromosomes, the DNA is tightly wound around proteins called histones
This complex on DNA wrapped around a histone is called a nucleosome
Start codon
At the start of every gene there is a 'Start codon' TAC in DNA or AUG in mRNA this codes for the amino acid methionine this methionine is later removed from the protein if it is not actually needed for the structure
Stop codon
At the end of every gene there are 3 bases that do not code for an amino acid and is known as a 'stop codon' These stop codons mark the end of a polypeptide chain and causes ribosomes to detach and therefore stop translation They are ATT, ATC and ACT on DNA
Degenerate
There are 20 amino acids that the genetic code has to be able to code for. There are 4 DNA bases and therefore 3 bases are needed to make enough combinations to code for at least 20 amino acids this can be proven mathematically (4^n)
Universal
The same triplet of bases codes for the same amino acid in all organisms this is why the genetic code is described as being universal
Advantage as it means genetic engineering is positive
Non-overlapping
Each base in a gene is only part of one triplet of bases that codes for one amino acid therefore each codon or triplet of bases is read as a discrete unit
Advantage as is a point mutation occurs it will only affect one codon and therefore one amino acid
Genome and proteome
The genome is an organism complete set of DNA in one cell, where as the proteome is the full range of proteins in one cell
The genome should never change whereas the proteome of the cell is constantly changing depending on which proteins are currently needed
The genome of organisms widely variers for example bacteria contain on average 6,000,000 DNA base pairs where as humans contain less base pairs
Introns and Exons
Introns are sections of DNA that do not code for amino acids and therefore polypeptide chains. Introns are found in eukaryotes DNA, but not in prokaryotic DNA. These get removed, spliced out of mRNA molecules
Exons are the sections of DNA that do code for amino acids
Proteins are created on ribosomes the production of proteins from the DNA code occurs in two main stages:
Transcription = Where one gene on the DNA is copied into mRNA
Translation = Where the mRNA joins with a ribosome and corresponding tRNA molecules brings the specific amino acid the codon codes for
This is the stage in which the polypeptide chain is created using both the mRNA base sequence and the tRNA
mRNA attaches to a ribosome in the cytoplasm
Ribosomes attaches at the start codon
The tRNA molecule with the complementary anticodon to the start codon
The ribosomes will move along the mRNA molecule
tRNA molecules are joined by a peptide bond this is catalysed by an enzyme and requires ATP
Continues until the stop codon - Then the ribosome detaches
The polypeptide chain is now created and will enter the Golgi body for folding and modification
Transcription
A complementary mRNA copy of one genes of the DNA is created in the nucleus
mRNA is much shorted than DNA so it is able to carry the genetic code to the ribosomes in the cytoplasm to enable the protein to be made
DNA helix unwinds
One chain of the DNA acts as a template
catalysed by DNA helicase
Breaks the Hydrogen bonds
Free mRNA nucleotides in the nucleus align
RNA polymerase bonds together
Once copied the mRNA is modified and then leaves the nucleus through the nuclear envelope pores
Pre - mRNA and mRNA
Following transcription, Pre mRNA has to be modified to become mRNA that is ready to leave the nucleus and take part in translation
The introns are spliced out by a protein called a spliceosome this leaves behind just the exons, the coding regions
Meiosis produces daughter cells that are genetically different from each other
Meiosis involves two nucleus divisions and creates 4haploid daughter cells from a single diploid parent cell.
There are two mechanisms in meiosis which introduce variation
Crossing over between homologous chromosomes
Independent segregation of homologous chromosomes
Both occur in meiosis 1
Independent segregation
In meiosis 1, homologous pairs of chromosomes line up opposite each other at the equator of the cell
It is random which side of the equator the paternal and maternal chromosomes from each homologous pair
These pairs are separated so one of each homologous pairs ends up in the daughter cell
This creates a large number of possible combinations of chromosomes in the daughter cells produced
Crossing over
When homologous pairs line up opposite each other at the equator in meiosis 1 parts of the chromatids can become twisted around each other
This puts tension on the chromatids causing pairs of the chromatids break
The broken parts of the chromatids recombine with the other chromatid
This result is new combination of alleles
Meiosis compared to mitosis
meiosis
Nuclear divisions
Haploid cell
Introduces genetic variation
Mitosis
One nuclear division
Diploid cells
Creates genetically identical cells
Final increase in genetic variation
Random fertilisation further increases genetic variation
There are 2n possible chromosomes combinations in gametes
It is random which egg and sperm will fuse in fertilisation therefore variation is increased
There is actually(2n)2 possible combinations of chromosomes when you consider random fertilisation
meiosis results in genetic variation
Mutations in the number of chromosomes can arise spontaneously by chromosome non-disjunction during meiosis
Non-disjunction is when chromosomes or chromatids do not split equally during anaphase
Chromosome non-disjunction
Changes in the number or structure of whole chromosomes can arise spontaneously due to chromosomes non-disjunction during meiosis
Chromosome non-disjunction can occur in two forms:
Changes in whole sets of chromosomes
Changes in the number of individual chromosomes
Polyploidy
Changes in whole sets of chromosomes occur when organisms have 3 or more sets of chromosomes rather then the usual two This condition is called polyploidy and mainly occurs in plants
Aneuploidy
Changes in the number of individual chromosomes
Sometimes individual homologous pairs of chromosomes fail to separate during meiosis
This is non-disjunction and usually results in a gamete having one more or one fewer chromosome
On fertilisation with a gamete that has the normal number of chromosomes, the resultant zygote will have more or fewer chromosome than normal in all their body cells
Genetic diversity
It is the number of different alleles of genes in a population
Natural selection can only occur if there is genetic diversity within a population
Natural selection
Natural selections is the process that leads to evolution in populations
Evolution is the change in allele frequently over many generations in a population
Natural selection results in species becoming better adapted to their environment
Adaptations may be anatomical physiological or behavioural
Directional selection
One of the extremes has the selective advantage
Occurs when there is a change in the environment
The model trait changes
Stabilising selection
The model traits has the selective advantage
Occurs when there is no change in the environment
The model trait remains the same
Standard deviation decreases, as individuals with the extreme trait decrease
Courtship behaviour is essential for successful mating and for species recognition
What is a species
A group of similar organisms that can breed to make fertile offspring
Species must reproduce and pass on advantageous alleles for the survival of their species
Courtship rituals
A sequence of actions which is unique to each species this is how animals identify members of their own species to reproduce with
Most courtship rituals are performed by males
They can include a sequence of dana moves, sounds, release of pheromones, display of colour feathers or fighting
Females observe the courtship ritual and decide if they wat to mate with the male
The importance of courtship
To ensure successful reproduction
enables them to recognise own species and opposite sex
Synchronises mating behaviour indicates sexually mature and in season
Binomial system
First name is genus, second name is species
Same genus shows close relationships
Why do different species look similar
Live in a similar environment
Have similar selection pressures
Similar alleles will have the selective advantage
Produces similar/same proteins and therefore have similar characteristics
Classification systems
Classification systems are an example of a hierarchy
Domain
Kingdom
Phylum
Class
Order
Family
Genus
Species
Ways to classify
Originally based on visible similarities
More modern and accurate classification methods are: