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Mitosis
makes 2 identical cells, for growth and repair
Meiosis
makes 4 genetically unique cells, for reproduction
Prophase
Chromatin condenses → forms visible chromosomes (X-shaped, 2 sister chromatids).
Mitotic spindle forms from centrioles (microtubule skeleton).
Nuclear envelope breaks down, nucleolus disappears.
Spindle fibers attach to kinetochores on centromeres.
Metaphase
Chromosomes line up along the metaphase plate (center of the cell).
Spindle checkpoint ensures all chromosomes are attached correctly.
Anaphase
Sister chromatids separate → pulled to opposite poles by spindle fibers.
Microtubules not attached to chromosomes push poles apart, elongating the cell.
Telophase
Chromosomes decondense back into chromatin.
Nuclear envelope reforms, nucleoli reappear.
Mitotic spindle breaks down.
Cytokinesis
Division of cytoplasm → results in 2 identical daughter cells.
Cleavage Furrow
how animal cells split
Cell plate
how plant cells split
Prophase, Metaphase, Anaphase, Telophase
Phases of Mitosis in order
Crossing over
homologous chromosomes swap segments → genetic variation
Spermatogenesis
Sperm → all 4 cells usable
Oogenesis
Egg → 1 viable egg + 3 polar bodies
Polysomy
extra chromosomes
Monosomy
missing chromosomes
Addition mutation
extra nucleotides
Deletion mutation
missing nucleotides
Translocation mutation
chromosome pieces swap
Direct reversal
fixes UV damage
Excision repair
removes damaged nucleotides
Post-replication repair
replication bypasses damage, fixes gap later
Transcriptional
control RNA polymerase access
Post-transcriptional
RNA splicing, alternative splicing, Poly-A tail, 5’ cap
Translational
Lac operon (inducible), Trp operon (repressible)
Post-translational
folding (chaperonins), modifications (glycosylation, phosphorylation)
miRNA
silences gene expression
Epigenetics
chemical marks turn genes on/off without changing DNA
Epistasis
one gene masks another
Hardy-Weinberg equilibrium conditions
no mutation, no migration, large population, no natural selection, random mating
p²
homozygous dominant in equations is represented by
2pq
heterozygous in equations is represented by
q²
homozygous recessive in equations is represented by
DNA sequencing
Sanger (old, precise), NGS (fast, cheap)
RNA-Seq
measures RNA expression
PCR
amplifies DNA
Gel electrophoresis
separates DNA/proteins by size/charge
Blotting (SNoW DRoP)
Southern = DNA, Northern = RNA, Western = protein
CRISPR-Cas9
guide RNA → Cas9 cuts DNA → repair or replacement
Plasmid cloning
small DNA circles carry genes into cells
Gene therapy
replace or fix faulty genes (experimental, risky)
Belmont Report principles
Respect, Beneficence, Justice
Prophase I
Chromosomes condense and become visible.
Homologous chromosomes pair up → form tetrads (4 chromatids).
Crossing over occurs → exchange of DNA segments between homologues → genetic variation.
Spindle fibers form, nuclear envelope breaks down.
Metaphase I
Tetrads line up
Random alignment → independent assortment → increases variation.
Anaphase I
Homologous chromosomes are pulled apart to opposite poles.
Sister chromatids stay together.
Telophase I & Cytokinesis
Nuclear envelope may reform; chromosomes may decondense.
Cytoplasm divides → 2 haploid cells.
Result of Meiosis 1
Each cell has one chromosome from each homologous pair, but still with two sister chromatids.
Prophase II
Chromosomes condense again (if they had decondensed).
Spindle fibers form, nuclear envelope breaks down.
Metaphase II
Chromosomes line up individually.
Anaphase II
Sister chromatids are now separated and pulled to opposite poles.
Telophase II & Cytokinesis
Nuclear envelopes reform, chromosomes decondense.
Cytoplasm divides → 4 haploid cells, each genetically unique.
Interphase
Most cells spend 90% of their time here.
G1 (Gap 1): Cell grows, makes proteins, duplicates organelles.
S (Synthesis): DNA is replicated → each chromosome now has 2 sister chromatids.
G2 (Gap 2): Cell grows more, checks DNA replication, repairs mistakes.
Checkpoints: G1 and G2 ensure DNA is intact and the cell is ready to divide.