E

Science Unit A Section 3

  1. DNA Structure

    • DNA (deoxyribonucleic acid) is a molecule that carries the genetic instructions for life.

    • Structure:

      • Double helix: Two strands twisted around each other.

      • Comprised of nucleotides: Each nucleotide consists of a sugar (deoxyribose), a phosphate group, and a nitrogenous base.

      • Four nitrogenous bases: Adenine (A), Thymine (T), Cytosine (C), and Guanine (G).

  2. Genetic Code and Genes

    • Genetic code: The sequence of nitrogenous bases that determines the traits of an organism.

    • Genes: Segments of DNA that code for proteins and influence traits.

  3. Nucleotides and Nitrogenous Bases

    • Nucleotides: The building blocks of DNA.

    • Nitrogenous bases pair specifically:

      • Adenine pairs with Thymine (A-T)

      • Cytosine pairs with Guanine (C-G)

  4. Mutations

    • Changes in the DNA sequence that may result in altered traits. They can be caused by environmental factors or occur randomly.

    • Types:

      • Point mutations (substitution of a single nucleotide)

      • Frameshift mutations (insertion or deletion of nucleotides)

  5. Chromosomes

    • Structures within cells that contain genes.

    • Humans have 23 pairs of chromosomes (46 total).

    • Chromosomal abnormalities can lead to disorders.

  6. Mitosis and Meiosis

    • Mitosis: Process of cell division resulting in two identical daughter cells; occurs in somatic (body) cells.

    • Meiosis: Process of cell division that reduces the chromosome number by half to produce gametes (sperm and eggs).

  7. Gametes

    • Reproductive cells produced during meiosis; contain half the number of chromosomes, essential for sexual reproduction.

  8. Trisomy Disorders

    • Trisomy: A condition where an individual has an extra chromosome.

      • Down syndrome (Trisomy 21): Caused by having three copies of chromosome 21, leading to developmental delays and characteristic physical features.

      • Klinefelter syndrome (XXY): Males have an extra X chromosome, leading to physical and hormonal changes.

  9. Dominant and Recessive Traits

    • Dominant traits: Traits that will appear in the offspring if one of the parents contributes them. Represented by a capital letter (e.g., A).

    • Recessive traits: Traits that will only appear if both parents contribute them. Represented by a lowercase letter (e.g., a).

  10. Codominance and Incomplete Dominance

    • Codominance: Both alleles are expressed equally in the phenotype (e.g., AB blood type).

    • Incomplete dominance: A blending of traits occurs (e.g., red and white flowers producing pink flowers).

  11. Hybrid and Purebred

    • Hybrid: Offspring resulting from the cross of two different purebred varieties (e.g., Aa).

    • Purebred: Offspring from parents of the same genetic type (homozygous, e.g., AA or aa).