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Homologous chromosomes: Chromosome pairs within cells which have the same sequence of genes. One chromosome of each pair comes from each of the parents through its gamete.
Gene: A sequence of DNA specifying the sequence of amino acids of a particular polypeptide.
Autosomes: Chromosomes that do not determine sex. Humans have 44 of them (22 pairs). The two remaining chromosomes determine sex and are known as the sex chromosomes.
Allele: An alternate form of a gene. A dominant allele masks the expression of another allele (and is commonly symbolized by a capital letter). The masked allele is recessive (and is commonly symbolized by the corresponding small letter).
Genotype: The combination of alleles in an individual (an individual's genetic constitution).
Phenotype: The observable expression of an allele combination.
Homozygous: Possessing two identical alleles of a gene. An individual with two dominant alleles is homozygous dominant. If both alleles are recessive, the individual is homozygous recessive.
Heterozygous: Possessing two different alleles of a gene.
Monohybrid: An individual heterozygous for a particular gene. In a monohybrid cross, two heterozygous individuals are mated. The expected genotypic ratio is 1:2:1 (i.e., AA, Aa, aa), and the expected phenotypic ratio is 3:1. To help derive these ratios, a diagram called the Punnett Square can be used.
Dihybrid: An individual who is heterozygous for two particular genes.
During meiosis, homologous pairs of chromosomes (and the genes that compose them) separate from one another and are packaged into separate gametes. At fertilization, gametes combine at random to form the individuals of a new generation.
By knowing the genotypes of the parents or the phenotypes of the offspring (assuming that there are enough to see all, or most of the possible phenotypes), it is possible to understand inheritance patterns, determine dominance of traits, and other genetic characteristics.
This sort of analysis was pioneered by Gregor Mendel (the "Father of Genetics") using peas. He scored different genetic lines for such characteristics as flower color, plant height, seed texture, and followed their inheritance patterns for many generations to determine the basic rules of inheritance.
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Punnett Square diagram of a monohybrid cross
Lastly, Mendel's Second Law (The Inheritance of Two Genes)
A gene on one chromosome does not influence the inheritance of a gene on a different (nonhomologous) chromosome because meiosis packages chromosomes randomly into gametes.
See last lecture's topic dealing with the independent assortment of chromosomes.
Can affect both sexes (because it is carried on a nonsex chromosome); AA or Aa have disorder; an affected individual must have an affected parent
Can affect both sexes; aa has disorder; can skip generations; carriers (Aa) occur and show no symptoms