OCR A Biology - key definitions

Subdecks (4)

Cards (757)

  • Allele
    A version of a gene
  • Allopatric speciation
    A form of speciation that occurs when two populations become geographically isolated due to a physical barrier
  • Apoptosis
    Programmed cell death. This is important for pruning surplus cells and tissues in development
  • Artificial selection
    See 'selective breeding'
  • Autosomal linkage
    When two or more genes are positioned on the same autosome. They are unlikely to be separated by crossing over during meiosis so are often inherited together
  • Autosome
    A chromosome that is not an X or Y chromosome
  • Bioinformatics
    The development of the computer tools and software required to organise and analyse unprocessed biological data
  • Chi-squared (X2) test

    A statistical test used to determine whether a pattern of inheritance is statistically significant
  • Chlorosis
    A condition in which plant leaf cells produce insufficient chlorophyll, resulting in pale or yellow coloured leaves. This may be due to mineral deficiencies, lack of light, or viral infections
  • Codominance
    When both alleles for a gene in a heterozygous organism equally contribute to the phenotype
  • Computational biology
    The use of computational techniques to analyse large amounts of biodata and build theoretical models of biological systems
  • Continuous variation
    A type of variation that cannot be categorised e.g. skin colour, height. It produces a continuous range in which a characteristic can take any value. Multiple genes influence continuous variation
  • Degrees of freedom (X2 test)
    The number of categories minus one
  • Deletion
    A form of gene mutation in which one or more nucleotide bases are removed from a DNA sequence. This may lead to a frameshift mutation, changing every successive codon
  • Dihybrid inheritance
    The determination of a trait by the inheritance of two genes
  • Directional selection
    A type of selection that favours one extreme phenotype and selects against all other phenotypes
  • Discontinuous variation

    A type of variation that can be categorised e.g. blood group. A characteristic can only appear in discrete values. One or two genes influence discontinuous variation
  • Disruptive selection
    A type of selection that favours individuals with extreme phenotypes and selects against those with phenotypes close to the mean
  • DNA barcode
    A short sequence of DNA that is used to identify a species. DNA barcodes are common to all species but vary between species
  • DNA ligase
    An enzyme that joins the sugar-phosphate backbone of two DNA segments
  • DNA profiling
    A technique used to determine the patterns in the non-coding DNA of an individual. It involves five main stages: DNA extraction; digestion; separation of DNA fragments; hybridisation; and observation
  • DNA sequencing
    Determining the entire DNA nucleotide base sequence of an organism
  • Dominant
    Describes an allele that is always expressed. Represented by a capital letter
  • Electrophoresis
    A type of chromatography that separates nucleic acid fragments or proteins by size using electric current
  • Electroporation
    A method of transformation in which a small electric current is used to transfer recombinant plasmids into bacterial cells or fragments of DNA into eukaryotic cells
  • Epistasis
    Describes a relationship between genes at different loci, where the allele of one gene affects the expression of a different gene
  • Etiolation
    A condition in plants characterised by weak stems and small, pale leaves, due to insufficient exposure to light
  • Evolution
    The gradual change in the allele frequencies within a population over time. Occurs due to natural selection
  • Exon
    A sequence of DNA that codes for an amino acid sequence
  • Founder effect
    A type of genetic drift in which a few individuals of a species break off from the population and form a new colony. This results in smaller gene pools and an increased frequency of rare alleles
  • Gene mutation
    A change to at least one nucleotide base in DNA or the arrangement of bases. Gene mutations can occur spontaneously during DNA replication and may be beneficial, damaging, or neutral
  • Gene therapy
    A therapeutic technique in which a faulty allele is replaced with a functional allele in order to treat or prevent disease
  • Genetically modified organism (GMO)

    An organism that has had its genome altered
  • Genetic bottleneck
    A drastic reduction in population size leading to reduced genetic diversity within a population
  • Genetic drift
    Random variations in allele frequencies in small populations, due to mutations
  • Genetic engineering
    The modification of the genome of an organism by the insertion of a desired gene from another organism. This enables the formation of organisms with beneficial characteristics
  • Genome
    The complete genetic material of an organism
  • Genotype
    An organism's genetic composition. Describes all alleles
  • Germ line cell gene therapy
    A type of gene therapy in which a faulty allele is replaced with a functional allele in germ cells or a very early embryo. The effects of this are permanent and can be inherited
  • Hardy-Weinberg principle
    A model that predicts that the ratio of dominant and recessive alleles in a population will remain constant between generations if the following five conditions are met: no new mutations; no natural selection; no migration; large population; and random mating. It provides a formula for calculating the frequencies of alleles: p2 + 2pq + q2 = 1.0 where p is the frequency of the dominant allele, and q is the frequency of the recessive allele