Heredity: The passing of traits from parent to offspring
Genetics: The study of heredity and variation
Gene: Segment of DNA molecule that codes for a particular trait
DNA (deoxyribonucleic acid): Carries genetic information in a cell
Locus: Location of a gene on a chromosome
Sexual reproduction: Individuals are produced by the fusion of two sex cells (genetically different from either parent)
Polyploid: Contain three or more sets of chromosomes. Many plants are polyploids
Asexual reproduction: New individual is produced from a single parent cell by cell division (genetically identical to parent)
Fragmentation: When an organism breaks down into several fragments, each fragment develops into an individual and is a clone of the original organism
Mitosis: The stage where the nucleus is divided. Two copies of the DNA separate to opposite ends of the cell. Each new nucleus has the same number of chromosomes and DNA as the original parent cell
Interphase: The longest phase where cells grow, perform normal functions, and prepare to divide by replicating DNA and organelles
Chromatin: The chromosomes form a tangled mass of DNA and protein
Sister chromatid: Identical copies formed by DNA replication of a chromosome, joined by a common centromere
Cytokinesis: The final stage of cell division where 2 separate cells are formed with a complete copy of the parent's DNA and organelles
Cloning: The process of producing offspring that are genetically identical to another, using a single cell or tissue
Biotechnology: Technology that utilizes biological systems, living organisms, or parts of this to develop or create different products
Genetically modified: Organism whose genetic material has been altered using genetic engineering techniques
Organism: All living things
Gamete: Sex cells. Male sex cell (sperm) and female sex cell (egg)
Fertilization: Sperm implanting in an egg
Zygote: Fertilized egg cell from the union of egg & sperm
Meiosis: Cell division that produces reproductive cells in sexually reproducing organisms
Homologous chromosome: Carry information for the same hereditary traits as its partner
Tetrad: A pair of homologous chromosomes, each with two sister chromatids
Synapsis: The physical pairing up of homologous chromosomes during prophase Ⅰ of meiosis
Crossing over: The exchange of chromosome segments between homologous pairs during synapsis
Gametogenesis: The formation of sex cells in meiosis
Spermatogenesis: The formation of sperm cells in the testes
Oogenesis: Formation of egg cells (ova) in the ovaries
Karyotype: Chromosomes of an individual sorted and arranged according to size and type
Sex chromosome: Located at the 23rd pair of homologous chromosomes
Autosomes: All other chromosomes that are not sex chromosomes
Nondisjunction: Failure of homologous chromosomes or sister chromatids to separate properly during cell division
Trisomy: 3 homologous chromosomes in place of a pair
Monosomy: Only one chromosome from a pair is present in cells rather than the two copies usually found in diploid cells
Down syndrome: Born with an extra chromosome 21
Prenatal testing: Ultrasound, Amniocentesis – uses a needle to inject into the womb and extract amniotic fluid to test fetal DNA
Mistakes in Meiosis:
Monosomy: Single chromosome in place of a homologous pair
Polysomy: A condition in which an organism has at least one more chromosome than normal
Down Syndrome: Condition in which a baby is born with an extra chromosome number 21
Aneuploidy: The condition of having an abnormal number of chromosomes in a haploid set