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Biology Exam 4 Review: Meiosis, Mendelian Genetics, Chromosomes & Inheritance, DNA Structure & Replication

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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'

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