Inheritance, variation and evolution

Cards (119)

  • Meiosis
    The formation of four non-identical cells from one cell
  • Mitosis
    The formation of two identical cells from one cell
  • Sexual reproduction
    Joining of male and female gametes, each containing genetic information from the mother or father
  • Gametes
    • Sperm and egg cells in animals
    • Pollen and egg cells in flowering plants
  • Gametes are formed by meiosis, as they are non identical
  • A normal cell has 46 chromosomes, in 23 pairs, one from each parent
  • Each gamete has 23 chromosomes and they fuse in fertilisation
  • The genetic information from each parent is mixed, producing variation in the offspring
  • Asexual reproduction
    One parent with no gametes joining, using mitosis to form two identical cells
  • Asexual reproduction leads to clones, which are genetically identical to each other and the parent
  • Organisms that reproduce asexually
    • Bacteria
    • Some plants
    • Some animals
  • Meiosis
    Cell makes copies of chromosomes, divides into two cells with half the chromosomes, then divides again to form four genetically different gametes
  • Gametes with 23 chromosomes join at fertilisation to produce a cell with 46 chromosomes
  • The cell divides by mitosis to produce many copies, forming an embryo which then undergoes differentiation
  • 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
    The genetic material in the nucleus of a cell, a chemical polymer with 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 disease and human migration
  • Nucleotide
    A small part of DNA, made up of a sugar, phosphate and one of four organic bases
  • A and T bases, and C and G bases, form complementary pairs in the DNA double helix
  • Protein synthesis
    DNA in nucleus transcribed to mRNA, mRNA transported to ribosomes, amino acids brought to ribosomes and joined to form protein
  • Mutation
    A change in the sequence of bases in DNA, can be an insertion, deletion or substitution
  • Most mutations do not alter the protein or only do so slightly, but some can have a serious effect on the protein structure and function
  • Gamete
    An organism's reproductive cell, with half the normal 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
  • Allele
    The different forms of a gene, humans have two alleles for each 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
    The combination of alleles an individual has
  • Phenotype
    The physical characteristics that are observed in the individual
  • 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