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Honors Biology Unit 5 Final Exam

  • Purpose of meiosis: to reduce the chromosome number from diploid to haploid and to generate genetic diversity among the producers

  • How many? 4 genetically distinct haploid cells

  • Which stages are diploid vs haploid? Prophase I and Metaphase I are diploid, then at the end of Anaphase I through Meiosis II, the cell is haploid

  • Major Events: Crossing over and synapse happens in Prophase I, Independent Assortment happens in Metaphase I and Nondisjunction can happen in Anaphase I and Anaphase II.

  •  Genetic Variability: Independent assortment, crossing over/synapse, and random fertilization

  • Difference between homologous and non-homologous chromosomes: Homologous chromosomes  are paired chromosomes with identical gene sequences, one from each parent, while non-homologous chromosomes have different genes and are not paired

  • Tetrad: a ground of 4 chromatids

  • Chiasma: where the homologous chromosomes are paired when crossing over

  • Centromere: what shapes the number of chromosomes and is in the middle where the sister chromatids join

  • Karyotype: a visual representation of an organism’s complete set of chromosomes, including their number, size, and shape

  • Nondisjunction:  the failure of chromosomes to separate. This happens in Anaphase I and Anaphase II

  • Chromosome deletion, duplication, inversion or translocation can disrupt normal gene function and lead to various genetic disorders.

  • True-breeder: a homozygous recessive individual

  • Hybrid: the offspring of two different parents

  • P generation: two individuals that are mated to foresee or analyze the genotypes of their offspring

  • F1 Generation: resulting offspring from the P0 generation

  • F2 Generation: the result of two F1 plants that were crossed or self-pollinated

  • Difference between incomplete and codominance? Incomplete dominance is the blending and mixing of alleles, creating a new phenotype, where as incomplete dominance is where you can see both allele present in the heterozygote

  • Test-Cross: the mating between an individual of unknown genotype and a true-breeding individual

  • Law of Independent Assortment: alleles of different genes assort independently during gamete formation

  • Pedigree Rules: if there is a 50/50 ratio between men and women that are affected, then the disorder is autosomal; if most of the males in the pedigree are affected, then the disorder is X-linked. If one of the parents have the disorder and it doesn’t skip generations then the disorder is dominant.

  • Pleiotropy: when one gene influences many characteristics/symptoms

  • Polygenic Inheritance: A single phenotypic character results from the additive effects of two or more genes.

  • Linked Genes: when two gene loci are close together, there is reduced chance for crossing over to occur between the two loci, which means they are linked. When the chi square problems donot follow normal mednelian outcomes is when the genes are linked.