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 in two sets of 23 pairs, 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, has double 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 chromosome shuffling
Gametes with 23 chromosomes join at fertilisation to produce a cell with 46 chromosomes
This cell divides by mitosis to produce many copies, an embryo forms, and cells begin to differentiate
Advantages of sexual reproduction
Produces variation in offspring
Allows selective breeding
Advantages of asexual reproduction
Only one parent needed
Uses less energy and is faster
Organisms using both sexual and asexual reproduction
Malarial parasites
Some fungi
Some plants
DNA
Genetic material in the nucleus, a polymer with 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 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
DNA structure
1. Made of nucleotides with sugar, phosphate, and one of four organic bases
2. Two strands with complementary base pairing (A-T, C-G)
3. Order of bases forms a code, three bases coding for one amino acid
4. Amino acids joined to form proteins
Protein synthesis
DNA in nucleus transcribed to mRNA, mRNA transported to ribosomes, amino acids brought and joined to form protein
Mutation
Change in DNA sequence, can insert, delete or substitute a base, affecting protein structure and function
Most mutations do not alter the protein or only do so slightly, some can have serious effects
Variation arises from coding DNA determining proteins and non-coding DNA controlling gene expression
Gamete
Reproductive cell with half the normal number of chromosomes
Chromosome
Structure in the nucleus made of a long strand of DNA
Gene
Short section of DNA coding for a protein, contributing to a characteristic
Allele
Different forms of the same gene, humans have two alleles per gene
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
Combination of alleles an individual has
Phenotype
The physical characteristics observed in the individual
Family trees show inheritance of phenotypes over generations
Punnett square diagrams can be used to determine probability of offspring genotypes and phenotypes
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