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Meiosis Stages and Chromosome Errors

Meiosis is a two-part cell division process that results in four haploid cells from one diploid cell. [1] The first phase (Meiosis I) separates homologous chromosomes, resulting in two haploid cells still containing sister chromatids. [2] Meiosis II then separates the sister chromatids, resulting in four haploid cells each containing one half the number of chromosomes of the original cell. [3] Meiosis ensures genetic diversity in sexual reproduction.
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0% found this document useful (0 votes)
16 views4 pages

Meiosis Stages and Chromosome Errors

Meiosis is a two-part cell division process that results in four haploid cells from one diploid cell. [1] The first phase (Meiosis I) separates homologous chromosomes, resulting in two haploid cells still containing sister chromatids. [2] Meiosis II then separates the sister chromatids, resulting in four haploid cells each containing one half the number of chromosomes of the original cell. [3] Meiosis ensures genetic diversity in sexual reproduction.
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GENERAL BIOLOGY 1 QUARTER 2

Stages of Meiosis ( Reduction Division)

One Chromosomes


Al

so known as Equation division


 Cell divides on somatic cells or body cells
 Significance: Centromere is the region
a. growth and development where the two sister
b. making of new body cells chromatids are held together
c. repair old and damaged cells/tissues after the replication of
 Produce identical diploid cells chromosome where
kinetochore is the protein
complex on the chromosome
Chromatin = DNA + Histone where spindle fibers are
attached during cell division.

WORDS TO REMEMBER
 MITOSIS- equation division
Body cells -somatic cells
 MEIOSIS- reduction division
Gametes -sex cells -germ cells
 In humans, each cell normally contains 23 pairs of
chromosomes, for a total of 46 chromosomes
 Twenty-two of these pairs, called autosomes (somatic or
body cells) look the same in both males and females
 The 23rd pair, the sex chromosomes (germ cells or gametes)
Chromatid is one of the two identical halves of a differ between males and females.
chromosome that has been replicated in preparation for cell  Females have two copies of the X chromosome, while males
division. have one X and one Y chromosomes.

Homologous Chromosomes

What is Meiosis?

 It is a process of cell division that takes place in sexually


mature organism.
 It results in the reduction of the chromosome number from
diploid to haploid in the sex cells (sperm cell and egg cell).
 It ensures the genetic continuity of species and through this
process, sexual reproduction results in genetic variety of the
members of a species.

HAPLOID vs. DIPLOID


PROPHASE 1

 Chromosomes condensed
and the nuclear envelope
 fragments.
 SYNAPSIS
 HOMOLOGOUS
CHROMOSOMES bind
firmly together along their
length, forming TETRAD.
 CHIASMATA form between
non-sister chromatids.
 CROSSING-OVER occurs at
the chiasmata.
 Spindle fibers emerge from the centrosomes

PROMETAPHASE 1- METAPHASE 1

 Homologous chromosomes
are attached to spindle
microtubules at the fused
kinetochores shared by the
PLOID vs. DIPLOID sister chromatids
 It is also proceeded by interphase (G1, S, and G2)  Chromosomes continue to
 G1 phase- focused on cell growth condense and the nuclear
 S phase- DNA replication Envelope completely
 G2 phase- final preparation for meiosis disappears.
 MEIOSIS I (P1, M1, A1, T1)= 2 diploid cells  Homologous chromosomes
 MEIOSIS 2 (P2, M2, A2, T2)= 4 haploid cells randomly assemble at
theMetaphase plate where they have been maneuvered
GENE vs. ALLELE into place by the microtubules
 RANDOM OR INDEPENDENT ASSORTMENT

ANAPHASE 1

 Spindle microtubules pull the


homologous chromosomes
apart.
 The sister chromatids are still
attached at the centromere

TELOPHASE 1
A gene is a portion of DNA that determines a certain trait.
An allele is a specific form of a gene. ...  Chromosomes(consisting
of sister chromatids)
IMPORTANT EVENTS DURING PROPHASE 1 arrive at the poles of the
cell and begin to
 Synapsis- tight pairing of homologous chromosomes decondense.
 Tetrad-results when chromosomes line up together  A nuclear envelope forms
 Chiasma- forms by cross-over recombination around each nucleus and
 Crossing-over- exchange of genetic materials the cytoplasm is divided
by a CLEAVAGE FURROW.
 The result is 2 DIPLOID
CELLS.
CYTOKINESIS 1 ANAPHASE 2

 Sister chromatids are


pulled apart by the
shortening of The
Kinetochore
microtubules.
 Non-kinetochore
microtubules
lengthen the cell.

TELOPHASE 2

 Chromosomes
arrive at the poles
of the cell and
decondense.
 Nuclear envelopes
surround the four
nuclei.
 CLEAVAGE
FURROWS divide
MEIOSIS 2 the two cells into
FOUR HAPLOID
CELLS.
 During meiosis II, the sister chromatids within the two
daughter cells separate, forming four new haploid gametes.
The mechanics of meiosis II is similar to mitosis, except that CYTOKINESIS 2
each dividing cell has only one set of homologous
chromosomes.

PROPHASE 2

 Chromosome
condensed.
 A new spindle
begins to form.
 The nuclear
envelops starts to
fragment

OVERVIEW OF MEIOSIS 2

PROMETAPHASE 2-METAPHASE 2
 The nuclear
envelope disappears
as the spindle fibers
engage the
individual
kinetochores on the
sister chromatids.
 Chromosomes line
up at the
metaphase plate
Errors in Mitosis and Meiosis

Mitosis
 The process by which cells make exact copies of
themeselves.
 One cell become two cell which grow to the same size as
the original cell making the organism grow.
 Many single-celled organisms reproduce in this way.
 Multicellular organisms use mitosis to grow and repair or
replace damaged worn out cells.
Errors in Mitosis

Edward’s syndrome (trisonomy 18)

 Almost every organ system


affected,
 1:10,000 live births.
 Children with full Trisomy
18 generally do not live m
ore tha a few months

 Generally due to non-disjunction (or failure to separate) of


Turner’s syndrome 45, (x0) females (trisonomy 18)
chromosomes or sister chromatids and may result to
chromosomal mutation.  A condition that affects only females, results when one of
 Mosaicism-is a consequence of mitosis passing on the the X chromosomes is missing or partially missing.
mutation to some cells.
*Hemophilia- a blood-clotting disorder
* Marfan’s syndrome- unusually long limbs
*Cancer
 Due to non-disjunction of homologous chromosomes during Klinefelter’s syndrome 47, XXY males
Meiosis I or II results to a sperm/egg cell that lacks one
chromosome or has an extra no. of chromosome.  Male sex organs; unusually small testes, sterile.
 Have 1 copy = monosomy = 45 chromosomes  Breast enlargement and other
 Have 3 copies = trisomy = 47 chromosomes  feminine body characteristics.
 Normal intelligence.
Down Syndrome/Trisomy 21/ Mongolism

Patau syndrome (trisonomy 13)

 Serious eye, brain, circulatory defects as well as cleft palate.


1:5000 live births. Children rarely live more than a few
months.

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