BackBiology Exam 4 Review: Meiosis, Mendelian Genetics, Chromosomes & Inheritance, DNA Structure & Replication
Study Guide - Smart Notes
Tailored notes based on your materials, expanded with key definitions, examples, and context.
CHAPTER 10 — MEIOSIS
Terminology
Understanding key terms is essential for mastering meiosis and inheritance.
Heredity: The transmission of traits from parents to offspring.
Variation: Differences among individuals in a population.
Genetics: The scientific study of heredity and variation.
Genes: Units of heredity made up of DNA; encode traits.
Gametes: Reproductive cells (sperm and egg) with half the chromosome number.
Somatic cells: All body cells except gametes; contain a full set of chromosomes.
Homologous chromosomes: Chromosome pairs, one from each parent, with similar structure and gene content.
Sexual vs. Asexual Reproduction
Organisms reproduce in two main ways, affecting genetic diversity.
Sexual reproduction: Involves fusion of gametes; offspring are genetically unique.
Asexual reproduction: Offspring arise from a single parent; genetically identical to parent.
Example: Bacteria reproduce asexually by binary fission; humans reproduce sexually.
Diploid (2n) vs. Haploid (n) Cells
Chromosome number distinguishes somatic cells from gametes.
Diploid (2n): Cells with two sets of chromosomes (e.g., human somatic cells, 2n = 46).
Haploid (n): Cells with one set of chromosomes (e.g., human gametes, n = 23).
Human Sexual Life Cycle and Role of Meiosis
Meiosis is central to maintaining chromosome number across generations.
Meiosis reduces chromosome number by half, producing haploid gametes.
Fertilization restores diploid number.
Alternation between diploid and haploid stages is key to the life cycle.
Events of Meiosis I and II
Meiosis consists of two consecutive divisions, producing four haploid cells.
Meiosis I: Homologous chromosomes separate.
Meiosis II: Sister chromatids separate.
Stages: Prophase, Metaphase, Anaphase, Telophase (I and II).
Example: In humans, meiosis produces sperm or eggs with 23 chromosomes.
Three Factors Contributing to Genetic Diversity
Meiosis and sexual reproduction generate variation.
Independent assortment: Random distribution of homologous chromosomes.
Crossing over: Exchange of genetic material between homologous chromosomes during Prophase I.
Random fertilization: Any sperm can fertilize any egg.
CHAPTER 11 — MENDELIAN GENETICS
Why Mendel Used Pea Plants
Gregor Mendel chose pea plants for their distinct traits, ease of cultivation, and controlled mating.
Pea plants have many observable traits.
Self-pollination and cross-pollination are possible.
Terminology
Dominant: Trait expressed when at least one dominant allele is present.
Recessive: Trait expressed only when both alleles are recessive.
Alleles: Different versions of a gene.
Genotype: Genetic makeup (e.g., AA, Aa, aa).
Phenotype: Observable traits (e.g., purple or white flowers).
Mendel’s P, F1, F2 Generations
Mendel tracked inheritance across generations.
P (parental): True-breeding parents.
F1 (first filial): Offspring of P generation; all showed dominant trait.
F2 (second filial): Offspring of F1; showed both dominant and recessive traits.
Monohybrid Crosses and Predicting Disorders
Monohybrid crosses examine one trait; used to predict inheritance of genetic disorders.
Cross between two heterozygotes (Aa x Aa) yields a 3:1 phenotypic ratio.
Example: Predicting cystic fibrosis inheritance.
Dihybrid Cross Phenotypic Ratio
Dihybrid crosses involve two traits.
Cross between two heterozygotes (AaBb x AaBb) yields a 9:3:3:1 phenotypic ratio.
Mendel’s Four Concepts
Genes exist in pairs (alleles).
Alleles segregate during gamete formation.
Dominance relationships determine phenotype.
Law of segregation: Each gamete receives one allele.
Law of Segregation
Alleles for a trait separate during gamete formation.
Explains why offspring inherit one allele from each parent.
CHAPTER 12 — CHROMOSOMES & INHERITANCE
Terminology
Wild-type: Most common phenotype in a population.
Mutant: Phenotype resulting from a genetic mutation.
Sex-linked: Genes located on sex chromosomes (X or Y).
Linked vs. unlinked: Linked genes are inherited together; unlinked genes assort independently.
Hemizygous: Having only one allele for a gene (e.g., males for X-linked genes).
X-linked Punnett Squares
Punnett squares are used to predict inheritance of X-linked traits.
Females (XX) can be homozygous or heterozygous; males (XY) are hemizygous.
Example: Color blindness inheritance.
Why X-linked Traits Affect Males
Males are more likely to express X-linked recessive traits.
Males have only one X chromosome; any recessive allele is expressed.
Females require two copies of the recessive allele.
Nondisjunction, Aneuploidy, Polyploidy
Errors in chromosome separation can lead to abnormal chromosome numbers.
Nondisjunction: Failure of chromosomes to separate properly during meiosis.
Aneuploidy: Abnormal number of chromosomes (e.g., trisomy 21).
Polyploidy: More than two complete sets of chromosomes (common in plants).
Chromosome Structure Alterations
Structural changes can affect gene function.
Deletions, duplications, inversions, translocations.
Example: Cri du chat syndrome (deletion on chromosome 5).
CHAPTER 13 — DNA STRUCTURE & REPLICATION
DNA Structure and Function
DNA is the hereditary material in cells, encoding genetic information.
Double helix structure discovered by Watson and Crick.
Stores, replicates, and transmits genetic information.
Nucleotide Components, Base Pairing, Purines vs. Pyrimidines
Nucleotides are the building blocks of DNA.
Nucleotide: Consists of a phosphate group, deoxyribose sugar, and nitrogenous base.
Base pairing: Adenine (A) pairs with Thymine (T); Guanine (G) pairs with Cytosine (C).
Purines: A and G; double-ring structure.
Pyrimidines: C and T; single-ring structure.
DNA vs. RNA; 5' vs. 3' Ends
DNA and RNA differ in structure and function.
DNA: Double-stranded, deoxyribose sugar, bases A, T, G, C.
RNA: Single-stranded, ribose sugar, bases A, U, G, C.
5' end: Phosphate group attached to the fifth carbon of sugar.
3' end: Hydroxyl group attached to the third carbon of sugar.
DNA Replication Enzymes; Leading vs. Lagging Strands
DNA replication is a complex process involving several enzymes.
Helicase: Unwinds DNA.
Primase: Synthesizes RNA primer.
DNA polymerase: Adds nucleotides to growing DNA strand.
Ligase: Joins Okazaki fragments on lagging strand.
Leading strand: Synthesized continuously.
Lagging strand: Synthesized in short fragments (Okazaki fragments).
Semiconservative Replication
Each new DNA molecule contains one old and one new strand.
Ensures accurate transmission of genetic information.
Equation:
Practice DNA Replication Example
Given a DNA template, predict the complementary strand.
Example: Template: 5'-ATGC-3' → Complement: 3'-TACG-5'