The formation of four non-identical cells from one cell
Mitosis
The formation of two identical cells from one cell
Sexual reproduction
1. Joining of male and female gametes, each containing genetic information from the mother or father
2. Sperm and egg cells in animals
3. Pollen and egg cells in flowering plants
Gametes are formed by meiosis, as they are non identical
Normal cell
Has 46 chromosomes, two sets of 23 chromosomes (one from each parent)
Gamete
Has 23 chromosomes, fuses in fertilisation
The genetic information from each parent is mixed, producing variation in the offspring
Asexual reproduction
1. One parent with no gametes joining
2. Happens using mitosis, where two identical cells are formed from one cell
3. No mixing of genetic information
4. Leads to clones, genetically identical to each other and the parent
Meiosis
1. Cell makes copies of chromosomes, doubling genetic information
2. Cell divides into two cells, each with half the chromosomes
3. Cell divides again producing four gametes, each with a quarter the chromosomes
4. Gametes are genetically different due to shuffling of chromosomes
Gametes with 23 chromosomes join at fertilisation to produce a cell with 46 chromosomes
This cell divides by mitosis to produce many copies, forming an embryo which then undergoes differentiation
Advantages of sexual reproduction
Produces variation in offspring
if the environment changes variation gives a survivaladvantage by naturalselection
Allows selectivebreeding
Advantages of asexual reproduction
Only one parent needed
Uses less energy and is faster
many identical offspring can be produced when conditions are favourable
Organisms using both sexual and asexual reproduction
Malarial parasites reproduce asexually in the human host, but sexually in the mosquito
Many fungi reproduce asexually by spores but also reproduce sexually to give variation
Many plants produce seedssexually, but also reproduce asexually by runners such as strawberry plants, or bulb division such as daffodils.
DNA
Genetic material in the nucleus of a cell, a polymer made up of two strands in a double helix structure
Gene
A small section of DNA on a chromosome that codes for a specific protein
Genome
All the genes coding for all of the proteins within an organism
The whole human genome has now been studied, improving understanding of genes linked to diseases, treatment of inherited disorders, and tracing human migration patterns
DNA structure
1. Made up of nucleotides, each with a sugar, phosphate, and one of four organic bases
2. Two DNA strands twisted together, with complementary base pairing (A-T, C-G)
3. Each group of three bases codes for an amino acid
4. The order of bases forms a code that determines aminoacids and proteins
Protein synthesis
1. DNA in nucleus cannot leave, so mRNA is made as a template
2. mRNA moves to ribosomes where amino acids are brought and joined to form a protein
3. Protein folds into a unique 3D structure
Mutations
Changes in the sequence of bases in DNA, can be insertions, deletions, or substitutions
Affect the amino acid sequence and protein structure
Most mutations do not alter the protein or only do so slightly, but some can have a serious effect
Variation between organisms arises from both coding DNA (determining proteins) and non-coding DNA (determining gene expression)
Gamete
An organism's reproductive cell, with half the number of chromosomes
Chromosome
A structure in the nucleus made up of a long strand of DNA
Gene
A short section of DNA that codes for a protein, contributing to a characteristic
Alleles
The different forms of a gene, humans have two alleles (one from each parent)
Dominant allele
Only one is needed to be expressed and observed
Recessive allele
Two copies are needed to be expressed and observed
Homozygous
Both inherited alleles are the same
Heterozygous
One inherited allele is dominant, the other is recessive
Genotype
The combination of alleles an individual has
Phenotype
The physical characteristics that are observed in the individual
Family trees show the inheritance of different phenotypes over generations
A Punnett square diagram can be used to determine the probability of offspring genotypes and phenotypes from two parents
Homozygous
When both inherited alleles are the same (i.e. two dominant alleles or two recessive alleles)
Heterozygous
When one of the inherited alleles is dominant and the other is recessive
Genotype
The combination of alleles an individual has, e.g. Aa
Phenotype
The physical characteristics that are observed in the individual, e.g. eye colour
Family trees show the inheritance of different phenotypes over generations in the same family