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gene
A segment of DNA that codes for a particular trait or protein — Ex: gene for eye color
homologous chromosomes
A pair of chromosomes (one from each parent) that have the same size, shape, and carry genes for the same traits — but may have different versions (alleles) of those genes
gamete
A reproductive sex cell (haploid) — Ex: sperm cell or egg cell
haploid
A cell containing only one set of chromosomes (n); half the full chromosome number — Ex: human sperm or egg cell — 23 chromosomes
diploid
A cell containing two complete sets of chromosomes (2n) — Ex: human somatic (body) cell — 46 chromosomes
meiosis
Cell division that produces 4 haploid gametes from one diploid cell; involves two divisions (Meiosis I and II)
crossing over
The exchange of genetic material between non-sister chromatids of homologous chromosomes during Prophase I; increases genetic diversity
trait
A characteristic that can be passed from parent to offspring — Ex: hair color, eye color, height
heredity
The passing of traits from parents to offspring
genetics
The branch of biology that studies heredity and variation in organisms
allele
Different versions of the same gene — Ex: allele for brown eyes vs. allele for blue eyes
dominant
An allele that masks the expression of the recessive allele; expressed when at least one copy is present — Written as a capital letter (e.g., B)
recessive
An allele whose expression is masked by the dominant allele; only expressed when two copies are present — Written as a lowercase letter (e.g., b)
homozygous
Having two identical alleles for a trait (either both dominant or both recessive) — Ex: BB or bb
heterozygous
Having two different alleles for a trait (one dominant, one recessive) — Ex: Bb
genotype
The genetic makeup of an organism; the alleles it carries — Ex: Bb, BB, bb
phenotype
The physical, observable expression of a genotype — Ex: brown eyes, tall height
law of segregation
Mendel's law stating that allele pairs separate during gamete formation; each gamete receives only one allele per gene
hybrid
An organism that is heterozygous for a trait (has two different alleles)
law of independent assortment
Mendel's law stating that genes for different traits are sorted independently during gamete formation (genes on different chromosomes)
true-breeding
An organism that always produces offspring with the same trait when self-pollinated (homozygous) — Ex: pea plants that always produce purple flowers
self-pollinating
A plant that can fertilize itself using its own pollen — Ex: Mendel's pea plants in controlled crosses
cross-pollinating
Transferring pollen from one plant to another to combine traits — Ex: Mendel crossing tall plants with short plants
P Generation
The parental generation; the original organisms crossed in a genetic experiment — Ex: true-breeding parents in Mendel's pea experiments
F₁ Generation
First filial generation; the offspring of the P generation cross — Ex: all tall plants when crossing true-breeding tall × short
F₂ Generation
Second filial generation; offspring produced by crossing or self-pollinating the F₁ generation — Ex: 3:1 ratio of tall to short plants
genetic recombination
The reshuffling of genes into new combinations through crossing over and independent assortment during meiosis
linked genes
Genes located on the same chromosome that tend to be inherited together
independent assortment
Process by which chromosomes independently sort into gametes, producing more possible genetic combinations
somatic cells
All body cells other than sperm or egg cells; they are diploid (2n)
Interphase (S Phase)
DNA replication occurs — chromosomes are copied before meiosis begins
Prophase I
Homologous chromosomes pair up forming tetrads; crossing over occurs; spindle fibers reach out to tetrads; nuclear membrane disappears
Metaphase I
Homologous chromosome pairs (tetrads) line up in the middle of the cell
Anaphase I
Homologous chromosomes separate and move to opposite ends of the cell (sister chromatids remain attached)
Telophase I
Chromosomes reach opposite sides; nuclear membrane begins to reform
Cytokinesis I
Cytoplasm divides to form two new cells (2n → n); each cell is haploid but chromosomes are still doubled
Prophase II
Spindle fibers start to reach out to centromeres of sister chromatids; nuclear membrane disappears in each cell
Metaphase II
Individual chromosomes (not pairs) line up in the middle of each cell
Anaphase II
Sister chromatids separate and move to opposite ends of each cell
Telophase II
Sister chromatids reach opposite sides; nuclear envelope reforms around each set of chromatids
Cytokinesis II
Cytoplasm divides again — forming 4 haploid daughter cells (gametes)
Interphase II
Brief resting stage between the two meiotic divisions; NO additional DNA replication occurs
Number of divisions
Mitosis: 1 cell division | Meiosis: 2 cell divisions
Daughter cells produced
Mitosis: 2 identical daughter cells | Meiosis: 4 genetically unique daughter cells
Chromosome number
Mitosis: chromosome number maintained (2n → 2n) | Meiosis: chromosome number halved (2n → n)
Genetic variation
Mitosis: no recombination — daughter cells identical to parent | Meiosis: crossing over and independent assortment create variation
Purpose
Mitosis: growth and asexual reproduction | Meiosis: production of gametes for sexual reproduction
Daughter cell identity
Mitosis: daughter cells are the same as the parent cell | Meiosis: daughter cells are NOT the same as the parent cell
Synapsis
Mitosis: does NOT occur | Meiosis: homologous chromosomes pair up (synapsis) in Prophase I
Produces gametes?
Mitosis: No | Meiosis: Yes
Chromosomes duplicated?
Both Mitosis AND Meiosis — chromosomes duplicate during Interphase (S Phase) before division
Where it occurs
Mitosis: all body (somatic) cells | Meiosis: ONLY in reproductive organs (gonads) to produce sperm or eggs
Homologous chr. behavior
Mitosis: homologous chromosomes do NOT pair up | Meiosis: homologous chromosomes pair up as tetrads in Meiosis I
Ploidy of result
Mitosis: diploid (2n) | Meiosis: haploid (n)
Associated with
Mitosis: asexual reproduction and growth | Meiosis: sexual reproduction and genetic diversity
Human diploid number
46 chromosomes (2n = 46) in all somatic body cells
Human haploid number
23 chromosomes (n = 23) in all gametes (sperm and egg)
Chromosomes after Meiosis I
23 chromosomes per cell (still consists of 2 chromatids each)
Chromosomes after Meiosis II
23 chromosomes per cell — now truly haploid single-chromatid chromosomes
Possible gamete combinations
Human chromosomes can combine in over 8 million possible ways (2²³) to form one sperm or egg
Fertilization combinations
When sperm and egg fuse, there are over 64 trillion possible chromosomal combinations — which is why we are all genetically unique
Sex chromosomes
Pair 23 — X and Y; females are XX, males are XY; all other 22 pairs are autosomes
Fertilization
When haploid sperm (23 chr.) and haploid egg (23 chr.) fuse → diploid zygote (46 chr.)
Where meiosis occurs in males
Males do NOT enter meiosis until after puberty; not all sperm enter at once — continuous production throughout life
Where meiosis occurs in females
Females are born with all future eggs (oocytes) stuck in Prophase I; one (or more) complete meiosis each month after puberty in response to hormones
Why siblings look different
Crossing over and independent assortment during meiosis increase genetic variation, giving up to 8 million possible gamete combinations per parent
Autosome pairs
Pairs 1-22 contain genes unrelated to sex determination; pair 23 = sex chromosomes
Genes passed per parent
Each parent has 2 copies of each gene and passes along only 1 copy to offspring
Tetrad
Structure formed when homologous chromosomes pair up in Prophase I; consists of 4 chromatids (2 pairs of sister chromatids)
Result of meiosis
4 haploid cells that are all genetically unique (not identical to each other or the parent)
Interphase II note
There is NO DNA replication between Meiosis I and Meiosis II — this is a key difference from the lead-up to mitosis