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Meiosis overview
Meiosis is a specialized form of cell division that reduces a diploid cell (2n) into four genetically unique haploid gametes (n). It involves one round of DNA replication followed by two consecutive divisions—Meiosis I and Meiosis II—generating genetic diversity through crossing over and independent assortment
Sexual reproduction combines gametes from 2 parents through fertilization
Mixing chromosomes from two parents increases genetic diversity

The Process of Meiosis
Animals have two sets of chromosomes: one set from each parent: they are called diploid (2n)
Reducing chromosomes by half is essential to avoid doubling in every generation
Gametes (egg and sperm) have one set of chromosomes. They are called haploid cells (1n)
Gametes
A haploid (1n) reproductive or sex cell that contains only one set of chromosomes (half the number of a normal somatic/body cell) and fuses with another gamete during sexual reproduction to form a diploid zygote
Haploid (1n) In humans, gametes contain 23 chromosomes (compared to 46 in somatic cells)
Egg and sperm
Gametes (egg and sperm) have one set of chromosomes. They are called haploid cells (1n)

Meiosis reduces the number of chromosomes by one half
Reductional Division (Meiosis I): Homologous chromosome pairs separate from each other, cutting the number of unique chromosome sets in half
Equational Division (Meiosis II): Sister chromatids separate (similar to mitosis), producing a total of four haploid (n) daughter cells from one diploid (2n) parent cell
The process through two rounds of division: Meiosis I
and Meiosis II

Egg (ovum)
An egg (ovum) is a haploid female gamete produced through the process of oogenesis via meiosis
Haploid (n): Contains a single set of chromosomes (23) chromosomes in humans), half the number of a somatic diploid (2n) cell
Unlike spermatogenesis (which yields four functional sperm), meiosis in females is asymmetric. It produces one large, functional egg cell and non-functional polar bodies that eventually degrade, conserving cytoplasm and nutrients for the potential zygote

Sperm
A haploid male gamete produced via meiosis that fuses with a female egg (ovum) during sexual reproduction to restore a diploid zygote
Haploid (n = 23 chromosomes in humans), carrying half the somatic cell genome.
Determines genetic sex in mammals: carries either an X chromosome (resulting in an XX female zygote) or a Y chromosome (resulting in an XY male zygote)
Contributes nuclear DNA to the zygote, while the egg contributes nuclear DNA, mitochondria, and most cytoplasmic organelle
Meiosis I
The first of two consecutive nuclear divisions in eukaryotic cell division. It is a reductional division that takes a diploid cell (with two sets of chromosomes) and separates homologous chromosome pairs to form two haploid daughter cells, each with half the original chromosome count
Chromosomes are replicated to make identical sister chromatids: DNA Replication (Interphase): Chromosomes copy their DNA to form two identical sister chromatids
Sister chromatids are attached at the centromere

S phase
The second stage of interphase, occurring before meiosis I, during which the cell replicates its DNA
DNA Duplication: each single chromosome is copied to form two identical sister chromatids joined together at the centromere by cohesin proteins
Genetic Content Change: the DNA amount doubles (from (2C) to (4C), while the actual number of chromosomes remains the same (2n)
Centrosome Replication: the centrosomes (which organize the meiotic spindle) also duplicate during this time
Chromosomes are duplicated during interphase (S phase)
The resulting sister chromatids are held together at the centromere
The centrosomes are also duplicated

Chiasmata
The X-shaped regions where crossing over has occurred between non-sister chromatids of homologous chromosomes
They form specifically between non-sister chromatids belonging to a tetrad (a pair of homologous chromosomes)
They represent the exact sites where genetic recombination (crossing over) occurred, allowing for the exchange of genetic material between maternal and paternal chromosomes
Crossing over occurs at the chiasmata

Tetrad
A group of four sister chromatids formed when two homologous chromosomes pair up side-by-side during prophase I of meiosis
a group of four closely associated chromatids formed when two homologous chromosomes pair up during prophase I of meiosis
Each of the two homologous chromosomes has already replicated into two sister chromatids, creating a total of four chromatids
They form via a process called synapsis, held together by a protein structure known as the synaptonemal complex
Tetrads are essential for crossing over (recombination), where non-sister chromatids exchange segments of maternal and paternal DNA

Crossing Over
The exchange of genetic material between non-sister chromatids of homologous chromosomes during prophase I of meiosis
occurs during Meiosis I (specifically in Prophase I)
At points called chiasmata, where homologous chromosomes physically connect (synapsis)
Non-sister chromatids (one from the maternal homologue and one from the paternal homologue), not sister chromatids (which are identical copies attached at the centromere)
It creates recombinant chromosomes with new allele combinations, significantly increasing genetic diversity in gametes

Prophase I
The first and longest stage of meiosis I, where homologous chromosomes pair up and exchange genetic material to create genetic diversity
Chromosomes condense and the nuclear envelope fragments
Homologous chromosomes bind firmly together along their length, forming a tetrad
Chiasmata form between non-sister chromatids
Crossing over occurs at the chiasmata
Spindle fibers emerge from the centrosomes

Synapsis
The physical pairing and alignment of homologous chromosomes that occurs exclusively during prophase I of meiosis I
During this process, maternal and paternal versions of the same chromosome find each other and tightly zip together lengthwise. This precise alignment is physically held together by a protein lattice called the synaptonemal complex
When homologous chromosomes undergo synapsis, they form a group of four closely associated sister chromatids known as a tetrad (or bivalent)
Synapsis aligns matching genes directly opposite one another. This alignment is required for crossing over (genetic recombination) to take place

Synapsis
The physical pairing and alignment of homologous chromosomes that occurs exclusively during prophase I of meiosis I
During this process, maternal and paternal versions of the same chromosome align precisely gene-for-gene. They are held tightly together by a zipper-like protein structure called the synaptonemal complex, forming a structure known as a tetrad (or bivalent)

Synaptonemal complex
A zipper-like protein structure that physically connects homologous chromosomes gene-by-gene during prophase I of meiosis I
Its primary function is to facilitate synapsis (the tight pairing of homologous chromosomes) and crossing over (homologous recombination), which allows non-sister chromatids to trade genetic material and create genetic diversity

Prometaphase I
The transitional phase of meiosis I that occurs between prophase I and metaphase
Homologous chromosomes are attached to spindle microtubules at the fused kinetochore shared by the sister chromatids
Chromosomes continue to condense
The nuclear envelope completely disappears

Metaphase I
The stage in meiosis I where homologous pairs of chromosomes (tetrads) align randomly along the equator (metaphase plate) of the cell, with spindle fibers attached to the kinetochores of each homolog
Homologous chromosomes randomly assemble at the metaphase plate, where they have been manuevered into place by the microtubules
The random orientation of each maternal and paternal pair along the equator is the physical basis of independent assortment, which drives genetic diversity in the resulting gametes
Homologous chromosome pairs (tetrads) line up randomly (indepdendant assortment) at the cell's equator (the metaphase plate)

What lines up at the metaphase plate during metaphase I?
During metaphase I of meiosis, homologous pairs of chromosomes (also called tetrads or bivalents) line up along the metaphase plate (the equator of the cell)
HOMOLOGOUS CHROMOSOME PAIRS LINE UP AT THE METAPHASE PLATE SIDE-BY-SIDE
What lines up: paired homologous chromosomes (each made up of two sister chromatids), rather than individual chromosomes
How they align: They line up side-by-side or stacked as pairs along the equator

What lines up at the metaphase plate during metaphase I?
During metaphase I of meiosis, homologous pairs of chromosomes (also known as tetrads or bivalents) line up along the metaphase plate (the equator of the cell)
What aligns: pairs of homologous chromosomes (each made up of two sister chromatids, for a total of four chromatids per tetrad) rather than individual chromosomes
In mitosis and meiosis II, individual replicated chromosomes line up in a single file line—not in homologous pairs

Difference between metaphase I and II
The main difference is how chromosomes align along the metaphase plate and the ploidy (chromosome number) of the cell
Metaphase I
Homologous pairs (tetrads) line up side-by-side along the metaphase plate (equator of the cell
Spindle fibers attach to the kinetochores of each homologous chromosome (one from each parent)
Next Step (Anaphase I): Homologous pairs separate, while sister chromatids stay attached
Metaphase II
Individual chromosomes (single file) line up along the metaphase plate, which looks identical to metaphase in mitosis
Spindle fibers attach to individual kinetochores on opposite sides of each chromosome's centromere
Next Step (Anaphase II): Sister chromatids separate and move to opposite poles, just like in mitosis

When does indepdendent assortment occur?
Independent assortment occurs during metaphase I of meiosis I
Random Orientation: during Metaphase I, homologous pairs of chromosomes line up in random, independent orientations along the metaphase plate (the middle of the cell)
This random alignment is a major contributor to genetic variation in sexual reproduction, along with crossing over (in Prophase I) and random fertilization
The 2^n Rule: The total number of possible chromosome combinations in the resulting gametes is calculated as 2^n, where n is the haploid number of chromosomes
23 chromosomes = 2²³
Indepdendent assortment
The principle that the alleles of two or more different genes get sorted into gametes independently of one another. In other words, the allele a gamete receives for one gene does not influence the allele it receives for another gene
It applies to genes located on different chromosomes (or far apart on the same chromosome). Genes that are very close together are "linked" and do not assort independently
It is a major source of genetic variation in sexually reproducing organisms. For example, humans have 23 pairs of chromosomes, leading to over 8 million (2²³) possible chromosomal combinations just from independent assortment alone

Independent assortment
The principle that the alleles of two (or more) different genes get sorted into gametes independently of one another. In other words, the allele a gamete receives for one gene does not influence the allele it receives for another gene
It occurs during Metaphase I of meiosis, when homologous chromosome pairs line up randomly at the cell's equator (metaphase plate)
It is one of the primary drivers of genetic variation in sexually reproducing organisms (along with crossing over in Prophase I and random fertilization)

Anaphase I
The stage of meiosis I in which homologous chromosome pairs separate and move toward opposite poles of the cell, while sister chromatids remain attached to each other at their centromeres
Spindle microtubules pull the homologous chromosomes apart
The sister chromatids are still attached at the centromere
Sister chromatids remain joined by cohesin proteins at the centromere
Reduction division: this is the step that reduces the cell from diploid (2n) to haploid (1n) because each pole receives only one chromosome from each homologous pair

Telophase I and Cytokinesis
Mark the end of the first meiotic division, converting a single diploid cell into two haploid cells
Sister chromatids arrive at the poles of the cells and begin to decondense
A nuclear envelope forms around each nucleus, and the cytoplasm is divided by a cleavage furrow
This results in two haploid cells
Each cell contains one duplicated copy of each homologous chromosome pair

End result of Meiosis I
Two haploid (n) daughter cells, each with duplicated chromosomes (consisting of two sister chromatids held together at the centromere)
The chromosome number is cut in half. Starting from one diploid (2n) parent cell, meiosis I produces cells that are now haploid (n) because homologous chromosomes separated, not sister chromatids
Even though the cells are haploid regarding the number of unique chromosome types, each individual chromosome is still composed of two sister chromatids (meaning DNA has not yet split into single-chromatid strands
Because of crossing over (synapsis and exchange of genetic material in Prophase I) and independent assortment (random orientation and separation of maternal and paternal homologs at the metaphase plate), these two daughter cells are genetically unique from each other and from the original parent cell

Prophase I
Homologous chromosomes pair. The synaptonemal complex holds them close together in synapsis
A pair of homologous chromosomes lined up next to each other during Prophase I of meiosis is called a tetrad or a bivalent
Non-sister chromatids of homologous chromosomes exchanged through crossing over (at the chiasmata, causing genetic diversity)
Crossing over occurs here

Prophase I structures
Structures at cross over points are called chiasmata
The four chromatids held together by chiasmata are called a tetrad
Chiasmata: the X-shaped regions where crossing over occurs between non-sister chromatids of homologous chromosomes during prophase I of meiosis
Tetrad: a group of four sister chromatids formed when two homologous chromosomes pair up side-by-side during prophase I of meiosis

Synapsis
The pairing of homologous chromosomes during prophase I of meiosis. This precise alignment allows for crossing over, where homologous chromosomes exchange genetic material to create genetic diversity
the lengthwise pairing of homologous chromosomes that occurs exclusively during prophase I of meiosis
Homologous chromosomes (one maternal and one paternal) physically align gene-for-gene. They are held tightly together by a protein structure called the synaptonemal complex

Synaptonemal complex
A zipper-like lattice of proteins that physically connects homologous chromosomes gene-for-gene during prophase I of meiosis
Facilitates Synapsis: It acts like a molecular zipper to bind maternal and paternal homologous chromosomes tightly together into a structure called a tetrad (or bivalent)

Crossover
Or chromosomal crossover, is defined as the exchange of genetic material between non-sister chromatids of homologous chromosomes
It takes place exclusively during prophase I of meiosis I.
The physical points where the chromatids overlap and intertwine are called chiasmata
Homologous chromosomes pair up gene-by-gene in a process called synapsis, forming a four-chromatid structure known as a tetrad
Crossover exchanges genetic material, increasing genetic diversity

Recombinant chromosomes
A chromosome that carries a new combination of alleles created when genetic material is exchanged between non-sister chromatids of homologous chromosomes
The mechanism: Crossing over (homologous chromosomes pair up as a tetrad and exchange matching segments of DNA at points called chiasmata)
Parental chromosomes: Keep the original combination of alleles inherited from the organism's mother or father
Recombinant chromosomes: Contain a mix of maternal and paternal alleles on a single chromatid

Non-recombinant chromosome
Also called a parental-type chromosome - is a chromosome that does not undergo any exchange of genetic material via crossing over during meiosis
Do not participate in crossing over (unaffected by a chiasma)
retains the exact combination of alleles (genes) that was originally inherited from one of the individual's parents

Metaphase I
Homologous chromosomes are arranged at the cell equator with kinetochores facing opposite poles
Maternal and paternal chromatids orient randomly and are mixed when they migrate to the poles
This creates additional genetic variation among daughter cells
Indepdendent assortment occurs here
The homologous pairs (one chromosome from the mother and one from the father) align side-by-side or in pairs along the cell's equator (the metaphase plate), rather than single file

Anaphase I
The stage of meiosis I in which paired homologous chromosomes separate and move toward opposite poles of the cell, while sister chromatids remain attached to each other at their centromeres
The microtubules pull tetrads apart
Chiasmata are broken but sister chromatids remain attached at centromere
This phase reduces the chromosome number from diploid (2n) to haploid (n)
Unlike mitosis or anaphase II where sister chromatids split, anaphase I separates whole homologous pairs
Nondisjunction can occur here

Nondisjunction
The failure of homologous chromosomes (during Meiosis I) or sister chromatids (during Meiosis II or mitosis) to separate properly during anaphase
Improper separation leads to daughter cells with abnormal chromosome numbers
Meiosis I Error: Homologous chromosomes fail to separate, resulting in 100% abnormal gametes
Meiosis II Error: Sister chromatids fail to separate, resulting in 50% abnormal gametes and 50% normal gametes

When can nondisjunction occur?
Nondisjunction can occur during anaphase in meiosis I, meiosis II, or mitosis when chromosomes or sister chromatids fail to separate properly
the failure of homologous chromosomes (during meiosis I) or sister chromatids (during meiosis II or mitosis) to separate properly during cell division
Trisomy: three copies of a chromosome (down syndrome/trisomy 21)
Monosomy: only one copy of a chromosome (Turner syndrome)
Telophase I and Cytokinesis
In meiosis I mark the final stage of the first reductional division, where chromosomes arrive at opposite poles of the cell, nuclear envelopes may reform, and the cytoplasm splits to produce two haploid daughter cells
Separated chromosomes arrive at opposite poles
Cytokinesis is separation of cytoplasmic contents into daughter cells and the nuclei reform
The cell's cytoplasm divides (via a cleavage furrow in animal cells or a cell plate in plant cells), physically separating the single cell into two distinct entities
Two haploid (n) daughter cells are formed. Crucially, each chromosome still consists of two sister chromatids, meaning the genetic material is not yet reduced to single-chromatid state (that happens later in Meiosis II)

End result of Meiosis I
At the end of Meiosis I, the single diploid (2n) parent cell has divided into two haploid (n) daughter cells

Cytokinesis in plants vs. animals
Cytokinesis in animal occurs via a cleavage furrow that
constricts
Plant cells form a cell plate that ultimately produces cell
walls that separate the daughter cells

Cytokinesis in plant cells
The physical division of the cytoplasm that follows nuclear division (telophase I and telophase II), using a cell plate mechanism due to the plant cell's rigid cell wall
Plant cells form a cell plate that ultimately produces cell
walls that separate the daughter cells

Cytokinesis in animal cells
The physical splitting of the cytoplasm that divides one cell into two distinct daughter cells. It occurs twice during meiosis (after Telophase I and after Telophase II)
Contractile Ring: a ring of microfilaments made of actin and myosin proteins forms just beneath the plasma membrane around the cell's equator
Cleavage Furrow: as the actin-myosin ring contracts (pulling like a drawstring), it pinches the plasma membrane inward from the outside-in
The indentation deepens into a cleavage furrow until the parent cell is completely pinched into two separate daughter cells

Meiosis II
The second round of cell division in meiosis, where sister chromatids separate to produce four genetically distinct haploid (n) gametes from the two haploid cells created in Meiosis I
Cells start haploid and end haploid.
No DNA Replication: there is no intervening S phase or DNA replication between Meiosis I and Meiosis II (only a brief interkinesis)
Sister Chromatids Split: unlike Meiosis I (which separates homologous chromosomes), Meiosis II splits the centromeres and pulls sister chromatids apart during anaphase II

Prophase II
The first stage of meiosis II, where the nuclear envelope breaks down, the nucleolus disappears, chromosomes condense again, and a new spindle apparatus begins to form in each of the two haploid daughter cells produced by meiosis I
Sister chromatids condense
A new spindle begins to form
The nuclear envelope starts to fragment
Functionally, Prophase II behaves very much like mitotic prophase, setting up the separation of sister chromatids in Anaphase II
Crossing over does not occur here (only prophase I)
Each cell entering prophase II is already haploid (n)

Prometaphase II
The transitional phase of cell division (occurring right after prophase and before metaphase) where the nuclear envelope breaks down and spindle fibers attach to the chromosomes
The nuclear envelope disappears
The spindle fibers engage the individual kinetochores on the sister chromatids

Metaphase II
The stage of meiosis II where individual chromosomes align single-file along the middle of the cell (at the metaphase plate), with spindle fibers attached to the kinetochores of each sister chromatid from opposite poles
Sister chromatids line up at the metaphase plate
Individual chromosomes (consisting of two sister chromatids) line up single-file, unlike Metaphase I where homologous pairs line up together
Haploid State: The cells entering metaphase II are haploid (n), meaning they have only one set of chromosomes rather than the diploid (2n) set found in mitosis or meiosis I
Microtubules attach to the opposite kinetochores of each centromere, setting up the separation of sister chromatids in the next phase

Anaphase II
The stage in meiosis II where the sister chromatids of each chromosome separate and move toward opposite poles of the cell
The proteins (cohesins) holding sister chromatids together break down, allowing them to pull apart
New status: once separated, each individual chromatid is officially classified as a distinct, single-stranded chromosome
Sister chromatids are pulled apart by the shortening of the kinetochore microtubules

Telophase II and Cytokinesis
The final stages of meiosis II. They complete the reduction and separation of genetic material, turning two haploid cells (with duplicated sister chromatids) into four genetically unique haploid gametes
Complete the second round of meiotic division, resulting in four genetically unique haploid (1n) cells (gametes)
Chromosomes arrive at the poles of the cell and decondense
Nuclear envelopes surround the four nuclei
Cleavage furrows divide the two cells into four gentically different haploid cells (1n)

End product of meiosis II
The end product of meiosis II is four genetically distinct haploid (n) daughter cells (gametes like sperm or egg cells)
The cells remain haploid throughout meiosis II. They start and end with half the chromosome number (\(n\)) of the original parent cell
Variations by Sex (Gametogenesis):
In spermatogenesis, it yields four functional haploid sperm cells.
In oogenesis, uneven cytokinesis typically yields one functional haploid egg (ovum) and polar bodies

End product of meiosis II
The end product of meiosis II is four genetically distinct haploid (n) daughter cells (gametes like sperm or egg cells)
The end product of meiosis II is four genetically distinct haploid (n) daughter cells (gametes like sperm or egg cells, or spores depending on the organism)

Prophase II
The first stage of Meiosis II, occurring in two haploid daughter cells left over from Meiosis I
Centrosomes migrate to opposite poles and new spindles form
Chromosome Condensation: chromatin re-condenses into visible, distinct chromosomes (each still composed of two sister chromatids).
Nuclear Envelope Breakdown: the nuclear envelope and nucleolus dissolve in each daughter cell.
Spindle Apparatus Formation: centrosomes (or MTOCs) duplicate and move toward opposite poles, starting to grow new spindle fibers.
No Crossing Over

Prometaphase II
A transitional sub-phase of Meiosis II that occurs after prophase II and right before metaphase II
Nuclear envelopes completely disappear
Spindle is fully formed
Each sister chromatid forms a kinetochore and attaches
to microtubules from opposite poles
The meiotic spindle apparatus finishes forming, and spindle microtubules capture the chromosomes by attaching to the kinetochores (protein structures located at the centromere of each sister chromatid)

Chromosome alignment differs between meiosis I and meiosis II
Chromosome alignment differs fundamentally between Meiosis I and Meiosis II in what is lining up at the metaphase plate and how the spindle fibers attach
Meiosis I
Homologous chromosome pairs (tetrads or bivalents) line up side-by-side along the metaphase plate during Metaphase I; maternal and paternal homologues face opposite poles randomly (independent assortment), creating genetic diversity
What separates: homologous chromosomes separate during Anaphase I, reducing the cell from diploid (2n) to haploid (n)
Meiosis II
Individual, replicated chromosomes (single-file) line up along the metaphase plate during Metaphase II—much like in mitosis
Attachment: sister chromatids attach to spindle fibers from opposite poles (bipolar attachment), just as they do during standard mitosis
Sister chromatids separate during Anaphase II, moving to opposite poles
The number of chromosomes per cell stays haploid (n→n), resulting in four unique haploid daughter cells total

Metaphase II and Anaphase II
Sister chromatids separate and move toward opposite
poles (similar to Mitosis)
Metaphase II
Alignment: The chromosomes (each consisting of two sister chromatids) line up individually in a single file along the cell's equator, known as the metaphase plate
Spindle Attachment: Spindle fibers (microtubules) from opposite poles attach to the kinetochores located at the centromeres of each chromosome
Anaphase II
Separation: the protein complexes holding sister chromatids together (cohesins) break down, causing the centromeres to split
Movement: the individual sister chromatids are pulled apart by shortening spindle fibers toward opposite poles of the cell

Telophase II and Cytokinesis
The chromosomes at opposite poles
Nuclear envelopes form around chromosomes
Cytokinesis separates the two cells into four unique haploid cells
Telophase II
Nuclear envelope reformation
Chromosomes decondense
Spindle breakdown
Cytokinesis II
Cytoplasm division: the physical division of the cytoplasm occurs simultaneously with or immediately following telophase II

Cytokinesis in plants vs. animals
The physical division of the cytoplasm occurs simultaneously with or immediately following telophase II
Cellular mechanism:
In animal cells, a contractile ring of microfilaments pinches the plasma membrane inward, forming a cleavage furrow
In plant cells, vesicles derived from the Golgi apparatus fuse along the metaphase plate to form a cell plate, which eventually develops into a new cell wall

Comparing meiosis and mitosis
Both processes divide the nucleus in eukaryotic cells
Mitosis is a single division; meiosis has two
Homologous chromosomes pair to form tetrads in meiosis
but not in mitosis
In meiosis, crossing over between sister chromatids and
random assortment of chromosomes in anaphase I create
genetic variation – mitosis produces genetically identical
clones
Meiosis reduces chromosomes (2n → 1n), mitosis does not

Comparing meiosis and mitosis
Both processes divide the nucleus in eukaryotic cells
Mitosis is a single division; meiosis has two
Homologous chromosomes pair to form tetrads in meiosis
but not in mitosis
In meiosis, crossing over between sister chromatids and
random assortment of chromosomes in anaphase I create
genetic variation – mitosis produces genetically identical
clones
Meiosis reduces chromosomes (2n → 1n), mitosis does not

Comparing meiosis and mitosis
Both processes divide the nucleus in eukaryotic cells
Mitosis is a single division; meiosis has two
Homologous chromosomes pair to form tetrads in meiosis
but not in mitosis
In meiosis, crossing over between sister chromatids and
random assortment of chromosomes in anaphase I create
genetic variation – mitosis produces genetically identical
clones
Meiosis reduces chromosomes (2n → 1n), mitosis does not

End product of mitosis vs. meiosis
Mitosis End Products
Number of cells: two daughter cells.
Chromosome number: diploid (2n) — identical to the parent cell (e.g., in humans, each cell has 46 chromosomes or 23 pairs)
Genetic identity: genetically identical to each other and to the original parent cell (barring rare mutations)
Purpose: somatic cell growth, tissue repair, asexual reproduction, and cell replacement
Meiosis End Products
Number of cells: four daughter cells
(Chromosome number): haploid (n) — half the number of chromosomes of the parent cell (e.g., in humans, each gamete has 23 single chromosomes)
Genetic identity: genetically unique/distinct from one another and from the parent cell

Meiosis Vs. Mitosis end products
Meiosis: four genetically unique haploid (n) daughter cells (gametes such as sperm or eggs) derived from a single diploid (2n) parent cell
Mitosis: two genetically identical diploid (2n) daughter cells

What causes genetic diversity during meiosis?
Crossing over (recombination) during prophase I of meiosis
Independent assortment during metaphase I
Random fertilization (occurs after meiosis, during sexual reproduction)
Nondisjunction
The failure of homologous chromosomes to separate properly during meiosis I or sister chromatids to separate properly during meiosis II (or mitosis)
Resulting Condition: leads to aneuploidy, a condition where cells have an abnormal number of chromosomes (such as 2n + 1 trisomy or 2n - 1 monosomy)
Nondisjunction occurs during meiosis I (anaphase I) or meiosis II (anaphase II), and can also occasionally happen during mitosis

Chromosome condensation
The process where long, thin chromatin threads tightly coil, fold, and pack into compact, distinct chromosomes
This structural transformation happens during prophase of mitosis and meiosis to prevent DNA damage and ensure accurate chromosome segregation
Makes chromosomes easier to seperate
Condensation packs the DNA into tight units. This makes it mechanically stable enough to be pulled apart by the spindle apparatus
chromatin condenses into distinct, visible chromosomes during prophase

What aligns during metaphase I?
During metaphase I of meiosis, homologous chromosome pairs (also known as tetrads or bivalents) line up along the metaphase plate (the equator) of the cell
homologous chromosome pairs (also called tetrads or bivalents) line up at the metaphase plate

What seperates in anaphase I?
During Anaphase I of meiosis, homologous chromosomes (homologs) separate and move to opposite poles of the cell
Sister chromatids stay attached: the centromeres do not split during Anaphase I, meaning sister chromatids remain joined together by cohesin proteins
homologous chromosomes (homologous pairs) separate and move toward opposite poles of the cell

When can nondisjunction occur?
Nondisjunction can occur during Anaphase I or Anaphase II of meiosis, as well as Anaphase of mitosis
Anaphase I of Meiosis I, Anaphase II of Meiosis II, or Anaphase of Mitosis
failure of chromosome pairs or sister chromatids to separate properly during cell division (anaphase)

What aligns in metaphase II?
Individual chromosomes (each composed of two sister chromatids) align single-file along the metaphase plate (the cell's equator)
Individual chromosomes (each consisting of two sister chromatids) align single-file along the metaphase plate (the equator of the cell)
Unlike Metaphase I—where homologous chromosome pairs line up together—Metaphase II features individual chromosomes lined up in a single file line, which looks very similar to metaphase in mitosis
What happens if nondisjunction occurs during meiosis 1?
Homologous chromosomes fail to separate during anaphase I. As a result, all four resulting gametes are abnormal: two gametes have an extra chromosome (n+1) and two gametes are missing a chromosome (n-1)
All four gametes are affected
Can be lethal for the baby
What happens if nondisjunction occurs during meiosis II?
When nondisjunction happens in meiosis II, sister chromatids fail to separate during anaphase II. This results in four total gametes: two normal haploid cells (n), one cell with an extra chromosome (n+1), and one cell missing a chromosome (n-1)
50% chance of an abnormal gamete
Centromere
The specialized, constricted region of a chromosome that holds two sister chromatids together after DNA replication and acts as the attachment site for spindle fibers during mitosis and meiosis
the specialized, constricted region of a chromosome that holds sister chromatids together and serves as the attachment site for spindle fibers during cell division

Kinetochore
A specialized protein complex assembled on the centromere of a chromosome where spindle fibers attach during cell division to pull sister chromatids apart
a large, disc-shaped protein complex that assembles on the centromere of a chromosome during cell division (mitosis and meiosis). It acts as the anchor point where spindle fibers (microtubules) attach to pull sister chromatids apart into separate daughter cells

Centrosomes
The primary microtubule-organizing center (MTOC) in animal and eukaryotic cells that builds the mitotic spindle to separate chromosomes during cell division
the main microtubule-organizing center (MTOC) of animal and many eukaryotic cells. It coordinates the microtubule cytoskeleton and builds the mitotic spindle during cell division
centrosomes contain centrioles and are surrounded by a protein complex

Centrioles
A small, cylindrical organelle made of microtubules (arranged in nine triplets) found in animal cells and located inside the centrosome
A pair of centrioles sits inside the centrosome (the main microtubule-organizing center or MTOC of animal cells), positioned at right angles
During mitosis and meiosis, centrosomes help organize the mitotic spindle fibers that attach to chromosomes and pull sister chromatids apart
small, barrel-shaped cell organelles found mostly in animal cells. They usually live in pairs inside a larger region called the centrosome, positioned at right angles to each other; made of microtubules

Cohesin
A ring-shaped protein complex that holds replicated sister chromatids together from the time they are synthesized (during S phase of interphase) until they separate during mitosis or meiosis
a protein complex that holds sister chromatids together from the time of DNA replication until they are separated during mitosis or meiosis

Spindle fibers
Bundles of microtubules that form the mitotic or meiotic spindle apparatus, responsible for moving and separating chromosomes during cell division
microscopic protein structures made of microtubules (composed of alpha- and beta-tubulin dimers) that organize and move chromosomes during eukaryotic cell division (mitosis and meiosis)

Microtublues
The largest component of the eukaryotic cytoskeleton, defined as hollow, rigid protein tubes made of polymerized dimers of a-tubulin and b-tubulin
Radiate from centrosomes to form the spindle apparatus, attaching to chromosomes at the kinetochore to separate sister chromatids during anaphase

Kinetochore microtubules
Specialized spindle fibers that bind directly to a chromosome's kinetochore—a protein structure built on the centromere region of a sister chromatids
Spindle microtubules that physically attach to the kinetochore protein complex on chromosomes
They shorten during anaphase to pull sister chromatids apart toward opposite poles of the cell

Chromosomes
A thread-like, gene-carrying structure found in the nucleus of eukaryotic cells, consisting of a single long molecule of DNA tightly wound and coiled around proteins called histones
a cellular structure composed of a single, long double-stranded DNA molecule tightly coiled and wrapped around histone proteins

Homologous chromosomes
A matched pair of chromosomes—one inherited from the mother and one from the father—that share the same length, centromere position, and gene sequence, though they may carry different alleles
a matching pair of chromosomes (one inherited from each parent) that carry the same genes in the same order. They pair up during prophase I of meiosis, swap segments through crossing over, and then separate in meiosis I so each gamete gets one of the pair

Chromatids
One half of a duplicated chromosome connected to its identical copy at a region called the centromere
one of two identical halves of a replicated chromosome joined together by a region called the centromere

Sister chromatids
Two identical copies of a single replicated chromosome. They are joined together at a specialized region called the centromere and share the exact same DNA sequence and alleles
the two identical copies of a single chromosome that are created during the S phase of interphase (DNA replication). They contain the exact same alleles and are held together by proteins called cohesins until they separate

Packaging of DNA
DNA wraps around histone proteins (like a string of beads)
The histone-DNA complex is called nucleosome
This structure then coils to form a chromatin fiber
The chromatin further packs into a chromosome

End product of meiosis
The end product of meiosis is four genetically unique haploid (n) daughter cells
Four daughter cells are produced from a single starting diploid (2n) cell
Haploid (n), meaning they contain half the chromosome number of the original parent cell
genetically distinct from one another and from the parent cell due to crossing over (prophase I) and indepdendent assortment (metaphase I)
