Unit 1 - Genetics

Cards (121)

  • Genetics
    The branch of biology dealing with heredity and the variation of inherited characteristics
  • Sexual reproduction
    Individuals are produced by the fusion of two sex cells (genetically different from either parent)
  • DNA (deoxyribonucleic acid)

    A molecule that carries genetic information in cells
  • Heredity
    The passing of traits from parent to offspring
  • Gene
    A segment of a DNA molecule that codes for a particular trait; found at a specific location on a chromosome
  • Locus
    The location of a gene on a chromosome
  • Polyploid
    Contain three or more sets of chromosomes. Many plants are polyploids
  • Interphase
    The longest phase. Cells grow and perform their normal function. Cell prepares to divide by replicating its DNA and organelles so they can be shared between the new cells
  • Chromatin
    The tangled strands of DNA and protein within a eukaryotic nucleus
  • Fragmentation
    A method of asexual reproduction in which a piece or body fragment of the parent organism develops into a mature individual
  • Mitosis
    The process by which a eukaryotic cell divides the genetic material in its nucleus into two identical nuclei
  • Organism
    A living thing that has an organized structure, can react to stimuli, reproduce, grow, adapt, and maintain homeostasis
  • Biotechnology
    The use and modification of organisms for applications in engineering, industry, and medicine
  • Sister chromatid
    The identical copy of a single chromosome that remains attached to the original chromosome at the centromere
  • Cytokinesis
    The final stage of cell division. 2 separate cells are formed - cytoplasm divides to form two identical cells
  • Asexual reproduction
    New individual is produced from a single parent cell by cell division (genetically identical to parent)
  • Gamete
    Sex cells (sperm and egg) are also known as gametes (sex cells). These have half the chromosomes
  • Genetically modified
    An organism in which the genetic material has been altered using genetic engineering techniques
  • Cloning
    The process of producing offspring that are genetically identical to another, using a single cell or tissue
  • Zygote
    A cell formed by the fusion of two sex cells. The zygote is diploid (2n)
  • Fertilization
    Sperm implanting in an egg. Results in the formation of a zygote (fertilized egg cell from the union of egg & sperm)
  • Synapsis
    The physical pairing up of homologous chromosomes during prophase Ⅰ of meiosis
  • Meiosis
    A form of cell division in which a single cell gives rise to four haploid daughter cells
  • Ova
    Female sex cells (egg cells)
  • Homologous chromosome
    Chromosomes that are not identical, they are similar in size, shape, and gene arrangement. Together these matching chromosomes are called a homologous pair
  • Crossing over
    The exchange of chromosome segments between homologous pairs during synapsis
  • Oogenesis
    The production of mature egg cells
  • Spermatogenesis
    The production of mature sperm cells
  • Sex chromosome
    Chromosomes that differ in males and females of the same species; the combination of sex chromosomes determines the sex of the offspring
  • Trisomy
    A chromosomal abnormality in which there are three homologous chromosomes in place of a homologous pair
  • Gametogenesis
    The production of gametes (sex cells) in animals
  • Karyotype
    The chromosomes of an individual that have been arranged and sorted according to size and type
  • Nondisjunction
    The failure of homologous chromosomes to move to opposite poles of the cell during meiosis; results in an abnormal number of chromosomes in the daughter cells
  • Autosomes
    Non-sex chromosomes
  • Down syndrome
    A chromosomal abnormality in which an individual has three copies
  • Monosomy
    A chromosomal abnormality in which there is a single chromosome in place of a homologous pair
  • iosis results in an abnormal number of chromosomes in the daughter cells
  • Trisomy
    A chromosomal abnormality with three homologous chromosomes in place of a homologous pair
  • Monosomy
    A chromosomal abnormality with a single chromosome in place of a homologous pair
  • Nucleotide
    The repeating unit in DNA comprising a deoxyribose sugar, a phosphate group, and one of the four nitrogenous bases