Steps of Meiosis:
Meiosis I:
Prophase I: Chromosomes condense, homologous chromosomes pair up (synapsis), crossing over occurs.
Metaphase I: Homologous pairs line up at the equator.
Anaphase I: Homologous chromosomes are pulled apart.
Telophase I: Two new cells form, each with half the chromosome number (haploid).
Meiosis II:
Prophase II: Chromosomes condense again in the two cells.
Metaphase II: Chromosomes align at the equator.
Anaphase II: Sister chromatids are pulled apart.
Telophase II: Four genetically different haploid cells result.
Gene pool
Bell-shaped; most individuals fall in the middle (average traits), fewer at extremes (rare traits).
Convergent: Unrelated species evolve similar traits (e.g., dolphins and sharks).
Divergent: Related species evolve different traits (e.g., Darwin’s finches).
Two species evolve in response to each other (e.g., flowers and pollinators, predator and prey).
Not inherited; only mutations in gametes (sex cells) contribute to genetic variation in offspring.
Homologous: Matching chromosomes from each parent.
Sister chromatids: Identical copies of a chromosome connected at the centromere.
Centromere: Region that joins sister chromatids.
Gene location: Specific locus on a chromosome.
Chromosomes in product: 23 (haploid in humans)
Number of cells: 4
Name of cells: Gametes (sperm or eggs)
Identical or different: Different due to crossing over and independent assortment
Meiosis I: Homologous chromosomes separate
Meiosis II: Sister chromatids separate
Occurs in Prophase I
Increases genetic variation by exchanging segments of DNA between homologous chromosomes
Male determines (XY); sperm can carry X or Y
Female is XX
Gregor Mendel
Complete dominance: One allele completely masks another (Aa = dominant trait)
Incomplete dominance: Blended phenotype (red + white = pink)
Co-dominance: Both alleles are expressed (AB blood type)
Multiple alleles: More than two possible alleles (blood type: A, B, O)
Sex-linked: Traits on X chromosome (e.g., color blindness)
Heterozygous individual who doesn’t express traits but can pass it on.
Females, because they have two X chromosomes.
Must have two recessive alleles (XᵃXᵃ)
Used to determine genotype of dominant individual by crossing with a homozygous recessive.
Involves two traits (AaBb x AaBb) – 9:3:3:1 phenotypic ratio typical
Multiple genes influence a trait (e.g., height, skin color)
Environment can influence phenotype (e.g., nutrition affects height)
Homozygous: Two of the same allele (AA or aa)
Heterozygous: Two different alleles (Aa)
Picture of chromosomes; shows chromosome number, sex, and large mutations
Family tree showing inheritance of traits
Genotype: Genetic makeup (e.g., Aa)
Phenotype: Physical appearance (e.g., tall)
Homozygous: Same alleles; Heterozygous: Different alleles
Gregor Mendel: Father of genetics, conducted experiments with pea plants and formulated the Laws of Inheritance (Law of Segregation and Law of Independent Assortment).
Thomas Hunt Morgan: A pioneering geneticist who worked with fruit flies and discovered the concept of sex-linked inheritance and genetic linkage.
Reginald C. Punnett: Co-developed the Punnett square for predicting genetic outcomes and worked on the study of genetic inheritance in pea plants.
Mendel’s experiment involved cross breeding pea plants that differed in traits such as flower color, seed shape, and plant height. By examining the ratios of traits in the F1 and F2 generations, he concluded that traits are inherited as discrete units (genes), and each parent contributes one allele for each trait to their offspring. He established the concepts of dominant and recessive alleles and the laws of inheritance.
Crossing over occurs during prophase I of meiosis, resulting in new combinations of alleles on chromosomes.
Independent assortment occurs during metaphase I of meiosis, where homologous chromosomes are randomly distributed to gametes, increasing variation.
Random fertilization occurs when any sperm can fertilize an egg, further increasing genetic variation.
Complete Dominance: One allele completely masks the expression of the other (e.g., TT = tall, Tt = tall, tt = short).
Incomplete Dominance: The heterozygote exhibits a blend of the two alleles (e.g., red + white = pink flowers).
Codominance: Both alleles are fully expressed in the heterozygote (e.g., red + white = red and white stripes).
Dihybrid Cross: Involves two traits (e.g., seed color and seed shape), requiring a 16-box Punnett square.
Multiple Alleles: More than two alleles exist for a gene (e.g., ABO blood types).
Sex-Linked Inheritance: Traits controlled by genes located on sex chromosomes, often X-linked, such as color blindness or hemophilia.
Polygenic Inheritance: Traits controlled by multiple genes, often resulting in a range of phenotypes (e.g., height, skin color).
Environmental Effects: The environment can influence the expression of genes (e.g., temperature-sensitive fur color in Siamese cats).
A testcross is used to determine the genotype of an individual expressing a dominant trait. If the individual is homozygous dominant, all offspring will express the dominant trait. If heterozygous, about half will express the recessive trait.
Punnett Squares: Be able to set up Punnett squares for all types of inheritance (monohybrid, dihybrid, incomplete dominance, codominance, etc.) and calculate genotype and phenotype probabilities.