All living organisms are composed of cells.
Cells can only be produced through the process of cell division, specifically Mitosis.
Somatic Cells: Non-reproductive cells in the body (e.g., skin, organs, muscles, bones).
Gametes: Reproductive cells (sperm/egg).
Diploid (2n): Humans have 23 pairs (46 total chromosomes).
Haploid (n): Gametes contain 23 single chromosomes.
Chromosomes: Structures made of DNA wrapped around proteins (histones), condense during cell division from loose chromatin to visible form.
Chromatids: The two identical halves of a chromosome.
Centromere: Structure that holds sister chromatids together.
Homologous Chromosomes: Chromosome pairs with the same genes but may carry different alleles (e.g., eye color).
Cells spend most time in Interphase (90%), compared to Mitosis (10%).
Interphase Stages:
G1 (Growth Phase 1): Rapid growth and replication of organelles.
S (Synthesis): DNA replication.
G2 (Growth Phase 2): Further growth and preparation for mitosis.
Prophase:
Nucleus present; chromosomes condense.
Mitotic spindle begins to form.
Metaphase:
Chromosomes align in the cell's equatorial plane.
Nucleus disassembled.
Anaphase:
Sister chromatids are pulled apart to opposite poles of the cell.
Telophase:
Chromatids arrive at poles; nuclear membranes reform, creating two nuclei.
The process that divides the cytoplasm, resulting in two daughter cells.
Involves one parent and produces clones without gametes.
Involves two parents combining genetic material through Meiosis.
Meiosis introduces genetic variation.
Two stages of cell division (Meiosis I and II).
Reduction Division: Halves chromosome number from 46 to 23.
Crossing Over: Genetic exchange during Prophase I increases diversity.
Independent Assortment: Chromosome pairs line up randomly, creating unique gene combinations.
Prophase I:
Chromatids condense; homologous chromosomes pair (crossing over occurs).
Metaphase I:
Pairs of chromosomes align in the middle.
Anaphase I:
Chromosomes pulled apart; sister chromatids remain together.
Telophase I:
Two new cells formed.
Prophase II:
Spindles form; no crossing over.
Metaphase II:
Chromosomes align in a single file in the middle.
Anaphase II:
Sister chromatids are separated.
Telophase II:
Nuclei reform; result in four haploid cells.
Errors in separation can lead to conditions from nondisjunction during anaphase I or II.
Inherited Trait: Traits passed down genetically.
Acquired Trait: Traits developed during life, not genetic.
Heredity: Process of passing traits through genes.
Genotype: Genetic makeup (pair of alleles).
Phenotype: Physical appearance of a trait.
Allele: Variants of a gene.
Homozygous: Two identical alleles (e.g., BB or bb).
Heterozygous: Two different alleles (e.g., Bb).
Dominant Allele: Expressed in phenotype (capital letters).
Recessive Allele: Only expressed when both alleles are recessive (lowercase).
Autosomes: Chromosomes 1-22, not gender-related.
Sex Chromosomes: Pair 23, determines biological sex (XX = female, XY = male).
F1 Generation: Offspring from two purebred parents; only dominant traits manifest.
F2 Generation: Result of F1's self-pollination; recessive traits reappear in a 3:1 ratio.
Each individual has two copies of each gene that segregate randomly into gametes during reproduction.
Focuses on one trait and its inheritance patterns.
Incomplete Dominance: Blending of traits (e.g., red and white flowers create pink).
Codominance: Both traits are fully expressed (e.g., AB blood type).
DNA is composed of deoxyribose sugars, phosphates, and bases (A, T, C, G).
RNA uses ribose and uracil instead of thymine.
Helicase: Unzips DNA strands.
DNA Polymerase: Builds the new strands of DNA.
Primase: Creates RNA primers for initiation.
Ligase: Seals DNA fragments together.
Transcription: DNA to mRNA in the nucleus.
Translation: mRNA to proteins with the help of ribosomes and tRNA.
Changes in the DNA sequence can lead to cancer or other genetic disorders.
Types of Mutations: Substitution, insertion, and deletion causes different effects on proteins.
Nonsense Mutations: Lead to premature stop codons, potentially producing nonfunctional proteins.
Involves cutting DNA with restriction enzymes, creating sticky ends, and sealing fragments to create new genetic combinations.
Producing transgenic organisms, such as bacteria making insulin, and DNA microarrays to observe gene activity.