BackCell Division, Genetics, and Inheritance: Study Guide for Biology 161 Test 4
Study Guide - Smart Notes
Tailored notes based on your materials, expanded with key definitions, examples, and context.
Mitosis, the Cell Cycle, and Apoptosis
Key Terminology
Sister chromatids: Identical copies of a chromosome connected by a centromere, formed during DNA replication.
Homologous chromosomes: Chromosome pairs (one from each parent) that are similar in length, gene position, and centromere location.
Phases of the Cell Cycle
G1 phase: Cell grows and carries out normal functions.
S phase: DNA is replicated, forming sister chromatids.
G2 phase: Cell prepares for division; checks for DNA errors.
M phase (Mitosis): Division of the nucleus and cytoplasm.
Events in Mitosis
Prophase: Chromosomes condense, spindle forms, nuclear envelope breaks down.
Metaphase: Chromosomes align at the metaphase plate.
Anaphase: Sister chromatids separate and move to opposite poles.
Telophase: Nuclear envelopes reform, chromosomes decondense.
Cytokinesis: Division of the cytoplasm, forming two daughter cells.
Bacterial Cell Division (Binary Fission)
Prokaryotes divide by binary fission, a simpler process involving DNA replication, segregation, and division of the cell.
Regulation of the Cell Cycle
Maturation Promoting Factor (MPF): A complex of cyclin and cyclin-dependent kinase (cdk) that triggers mitosis.
Checkpoints: Control points (G1, G2, M) where the cell assesses readiness to proceed; tumor suppressor genes (e.g., p53) help regulate these checkpoints.
Social control/signal transduction: Proto-oncogenes promote cell division in response to signals; different cyclins and cdks regulate specific cell cycle phases.
Cancer: Characterized by uncontrolled cell division, often due to mutations in proto-oncogenes or tumor suppressor genes; follows the multi-hit hypothesis (multiple mutations required).
Apoptosis – Programmed Cell Death
Occurs during development, in response to DNA damage, or to remove unneeded cells.
Process involves DNA fragmentation, formation of apoptotic bodies, membrane blebbing, and activation of macrophages to clear debris.
Meiosis and Genetic Recombination
Key Terminology
Haploid (n): One set of chromosomes.
Diploid (2n): Two sets of chromosomes.
Aneuploid: Abnormal number of chromosomes.
Lifecycles: Animals vs Plants
Animals: Gametes (sperm, egg) are haploid; fertilization restores diploid state.
Plants: Alternate between multicellular haploid (gametophyte) and diploid (sporophyte) generations.
Events in Meiosis
Meiosis I: Homologous chromosomes separate.
Meiosis II: Sister chromatids separate (similar to mitosis).
Order: Prophase I, Metaphase I, Anaphase I, Telophase I, then Prophase II, Metaphase II, Anaphase II, Telophase II.
Differences Between Meiosis and Mitosis
Mitosis produces two genetically identical diploid cells; meiosis produces four genetically unique haploid cells.
Meiosis includes crossing-over and independent assortment, increasing genetic diversity.
Sources of Genetic Variation
Crossing-over: Exchange of genetic material between homologous chromosomes during Prophase I.
Independent assortment: Random orientation of homologous pairs during Metaphase I.
Random fertilization: Any sperm can fertilize any egg, further increasing variation.
Oogenesis vs Spermatogenesis
Oogenesis: Produces one egg and polar bodies; occurs in ovaries.
Spermatogenesis: Produces four sperm; occurs in testes.
Genetics (Mendelian and Non-Mendelian)
Mendel’s Experiments and Laws
Studied inheritance in pea plants; deduced the laws of segregation and independent assortment.
Key Terminology
Allele: Alternative form of a gene.
Gene: Unit of heredity.
Homozygous: Two identical alleles.
Heterozygous: Two different alleles.
Dominant: Expressed allele in heterozygote.
Recessive: Masked allele in heterozygote.
Genotype: Genetic makeup.
Phenotype: Observable traits.
Genotypic and Phenotypic Ratios
Monohybrid cross: 3:1 phenotypic ratio (dominant:recessive) in F2 generation.
Dihybrid cross: 9:3:3:1 phenotypic ratio in F2 generation.
Testcross
Used to determine the genotype of an individual with a dominant phenotype by crossing with a homozygous recessive.
Punnett Squares and Probability
Visual tool to predict offspring genotypes and phenotypes.
Multiplication rule: Probability of independent events occurring together is the product of their probabilities.
Addition rule: Probability of either of two mutually exclusive events is the sum of their probabilities.
Non-Mendelian Inheritance Patterns
Incomplete dominance: Heterozygote shows intermediate phenotype (e.g., pink flowers from red and white parents).
Codominance: Both alleles expressed (e.g., AB blood type).
Multiple allelism: More than two alleles for a gene (e.g., ABO blood group).
Polygenic traits: Multiple genes affect a trait (e.g., skin color).
Epistasis: One gene affects expression of another gene.
Pleiotropy: One gene influences multiple traits.
Gene x environment: Environmental factors influence gene expression (e.g., temperature-sensitive fur color in rabbits).
Pedigree Analysis
Used to determine inheritance patterns (autosomal or X-linked, dominant or recessive) in families.
Telomeres and Telomerase
Telomeres: Protective ends of chromosomes that shorten with each division.
Telomerase: Enzyme that extends telomeres, active in germ cells and some cancer cells.
DNA Proofreading and Repair Mechanisms
DNA polymerases proofread and correct errors during replication.
Repair mechanisms (e.g., mismatch repair, excision repair) fix DNA damage.
Higher Order Thinking Questions (with Academic Context)
Compare and contrast mitosis and meiosis: Both involve chromosome duplication and division, but mitosis produces two identical diploid cells for growth/repair, while meiosis produces four unique haploid cells for sexual reproduction.
Cell cycle regulation: Ensures cells divide only when appropriate; loss of control can lead to cancer or apoptosis.
Cytoplasmic factors and mitosis: Cytoplasm from dividing cells contains MPF (cyclin + cdk), which can induce mitosis in non-dividing cells by activating mitotic processes.
Crossing-over: Occurs during Prophase I of meiosis; increases genetic diversity but improper crossing-over can cause chromosomal mutations.
Oogenesis chromatid count: Human oogonium (2n) duplicates DNA (4n chromatids), then meiosis I and II reduce to one egg (n) with one chromatid per chromosome.
Genetic cross ratios:
3:1 – Monohybrid cross (heterozygotes)
9:3:3:1 – Dihybrid cross (independent assortment)
1:1:1:1 – Testcross with dihybrid
1:1 – Testcross with monohybrid
1:2:1 – Incomplete dominance or codominance in monohybrid cross
Pedigree analysis: Sex-linked recessive traits often skip generations and affect more males; autosomal recessive traits affect both sexes equally. Dominant traits appear in every generation; X-linked dominant traits affect both sexes but often more females.
Dominant traits: Determined by allele function, not prevalence. Example: In Mendel’s peas, yellow seed color is dominant but not necessarily most common. Dominance results from the gene product’s function or mutation effects.
Extensions to Mendel’s laws: Simple dominance (one allele masks another), incomplete dominance (blended phenotype), codominance (both alleles expressed).
Table: Comparison of Mitosis and Meiosis
Feature | Mitosis | Meiosis |
|---|---|---|
Number of divisions | 1 | 2 |
Number of daughter cells | 2 | 4 |
Genetic composition | Identical to parent | Genetically unique |
Chromosome number | Diploid (2n) | Haploid (n) |
Role | Growth, repair | Gamete production |
Key Equations
Probability of independent events:
Probability of mutually exclusive events: