meiosis - chandler unified school district3/25/2013 4 meiosis four haploid cells (n) each have one...
TRANSCRIPT
3/25/2013
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MEIOSIS Genetics Unit
LIVING ORGANISMS
2 types of cells:
Autosomal (body) cells have 2 copies of every gene
Gametes (sex) cells have 1 copy of every gene
CHROMOSOME NUMBER
Autosomal (body) cells
Humans 46
Gametes (sex) cells
Sperm & Egg cells
Female XX
Male XY
Willie Shoemaker, Wilt Chamberlain
~taken by Annie Liebowitz
3/25/2013
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SEXUAL REPRODUCTION
Sexual reproduction provides variation due to the
shuffling and recombination of alleles during
meiosis and fertilization
99.99% of our DNA is the same
MEIOSIS is what makes us different!
WHAT IS INHERITED?
Genes – sequence of DNA, that codes for a protein,
that determines a trait
Genes are located on chromosomes (supercoiled
DNA)
Humans have 46, or 23 “homologous” pairs
Half from mom,
Half from Dad
WHY MEIOSIS?
Cell division to make gametes, or sex cells
Sperm in males
Eggs in females
Why would it be
different than Mitosis?
Diploid (2n) – contains a
pair of each chromosome;
mitosis
Haploid (n) – contains only
1 of each chromosome;
meiosis
3/20/13
Objective
Illustrate the steps to meiosis
Warm-Up
1. Multiply (x + 5)(x – 5)
2. How many copies of a gene do body (autosomal)
cells have? How many do sex (gamete) cells
have?
EX. 2N = 4
MEIOSIS I
Prophase I
Tetrads form – homologous
chromosomes pair
Cross-Over occurs –
homologous chromosomes
exchange part of their
chromatin
Produces new gene
combinations!
All other events same as
mitosis
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GENETIC VARIATION: CROSSING OVER
Homologous chromosomes group together and exchange pieces.
http://www.youtube.com/watch?v=D1_mQS_FZ0&feature=related
Meiosis I
Crossing
over
MEIOSIS I
Metaphase I
Tetrads line up randomly
on the metaphase plate
Increases variation!
Anaphase I
Homologous chromosomes
are pulled apart
Telophase I
Same events as in mitosis
EXCEPT… now the
daughter cells are Haploid
Prophase I Metaphase I Anaphase I Telophase I
and
Cytokinesis
Interphase I
Meiosis I
MEIOSIS I
MEIOSIS II Exactly like Mitosis; sister chromatids separate
Telophase II
and
Cytokinesis
Prophase II Metaphase II Anaphase II Telophase I and
Cytokinesis I
Meiosis II
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MEIOSIS
Four haploid cells (n) each have one chromosome.
Each cell has a different combination of
alleles.
GENETIC VARIATION: PRINCIPLE OF
INDEPENDENT ASSORTMENT
GENETIC VARIATION: RANDOM
FERTILIZATION
Many possible combinations of male and female
gametes.
HUMANS
There is a 50% chance that a particular gamete
will receive a maternal chromosome and a 50%
chance it will receive a paternal chromosome.
There are 23 pairs of chromosomes in human games
cells.
Number of possible combinations of maternal
and paternal chromosomes= 223
HUMANS
One human ovum (egg) represents approximately
8 million possible chromsome combinations.
Same is true for sperm. Thus, one sperm
fertilizing one egg results in 8 million x 8 million
recombination possibilities
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MEIOSIS SQUARE DANCE
http://teachersites.schoolworld.com/webpages/DC
urry/life.cfm?subpage=1151190
MEIOSIS FOLDABLE
MALES VS. FEMALES
Males produce 4 haploid gametes (sperm)
Females produce 1 haploid gamete (egg) + 3
“polar bodies”
3/22/13
Objective
Illustrate meiosis
Warm-Up
Subtract (5p2 – 3) – (2p3 – 3p2)
What happens during prophase I that allows for
genetic variation?
3/25/13
Objectives
Differentiate between mitosis and meiosis
Warm-Up
1. Simplify (2m2)(2m3)
2. What is the goal of meiosis I?
3. What is the goal of meiosis II?
AIMS is just
around the
corner!
MITOSIS VS. MEIOSIS
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MITOSIS VS. MEIOSIS
Mitosis Meiosis
Type of cell Body Cell Sex cell
Beginning cell Diploid (2n) Diploid (2n)
Ending cell Diploid (2n) Haploid (n)
# of cells produced 2 4
# of chromosomes
Same as parent cell Half as parent cell
Purpose
To make more body
cells
To make egg and
sperm
EX. 2N = 4
Haploid
Diploid
Different
Identical
Haploid
*Cross-Over
*Random
Orientation
MITOSIS VS. MEIOSIS
Meiosis:
Random orientation of chromosomes
Crossing over
Random fertilization
Independent assortment
Occurs in 2 phases
Creates 4 different cells (haploid)
Mitosis:
Creates 2 genetically identical cells (diploid)
MEIOSIS LAB
PRACTICE
A human has 23 pairs of chromosomes.
1. What is the diploid number?
2. What is the haploid number?
3. How many chromosomes are in an egg cell?
4. How many chromosomes are in a brain cell?
5. How many chromosomes are in a skin cell?
6. How many pairs of homologous chromosomes?
7. How many chromosomes in a cell produced by
mitosis?
8. How many chromosomes in a cell produced by
meiosis?
MEIOSIS
OREO COOKIE LAB PICTURES
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COOKIES
Blue: 1 Pair of Homologous Chromosomes
Pink: 1 Pair of Homologous Chromosomes
Red: Nuclear Envelope
Green: Meiotic Spindles
Brown: Centrioles
COMPLETED OREO COOKIE LAB Blue: 1 Pair
of Homologous Chromosomes
Pink: 1 Pair of Homologous Chromosomes
Red: Nuclear Envelope
Green: Meiotic Spindles
Brown: Centrioles
PROPHASE I METAPHASE I
Crossover
Random orientation
ANAPHASE I TELOPHASE I
PROPHASE II METAPHASE II ANAPHASE II TELOPHASE II
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PROBLEMS WITH
MEIOSIS
Nondisjunction
THIS IS WHAT YOUR CHROMOSOMES LOOK
LIKE DURING MITOSIS.
Scientists take a
picture of the
chromosomes, like
this one, and cut
then them out…
…AND THEN GROUP THEM TOGETHER BY
SIZE.
Karyotype –
picture of
chromosomes
grouped as pairs
Humans-46
chromosomes;
23 pairs
KARYOTYPES ARE MADE MOST OFTEN
DURING PREGNANCY IN A PROCEDURE
CALLED AN AMNIOCENTESIS.
Amniocentesis – The baby’s amniotic fluid cells are taken from the womb through a needle, and a karyotype is made to look for disorders.
PROBLEMS SHOW UP WHEN THE BABY
HAS THE WRONG NUMBER OF
CHROMOSOMES.
What is wrong with this karyotype?
THIS KARYOTYPE SHOWS THAT THE
PERSON HAS THREE OF CHROMOSOME 21.
THIS CAUSES THE BIRTH DEFECT DOWN
SYNDROME.
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DOWN SYNDROME – “TRISOMY 21”
Children with Down Syndrome have a variety of problems, including mild mental retardation, heart
problems, and many other unusual physical characteristics.
Nondisjunction – When chromosomes
fail to separate during meiosis.
Down Syndrome occurs when two sister chromatids fail to separate during anaphase of meiosis II. As a result, some of the eggs or sperm produced have too many chromosomes.
When a cell ends up with three copies of a
chromosome instead of two, this is called
trisomy. If a cell has only one copy, this is
called monosomy.
OTHER NONDISJUNCTION DISORDERS:
Klinefelter’s Syndrome (XXY) Males w/an extra X
Small testicles, reduced fertility
Turner’s Syndrome (X__) Girls w/1 X
Short stature, swelling, sterility
Triple X Syndrome (XXX) Girls w/3 X chromosomes
Tall, but normal physical and sexual characteristics
Increased risk of learning disabilities
Slow speech and motor development
Edward Syndrome (trisomy 18) Only 5-10% of live births survive the
1st year of life
Many abnormalities in internal organs and external structures
NONDISJUNCTION IS MOST LIKELY TO HAPPEN
IN OLDER MOTHERS, BECAUSE THEIR EGGS
HAVE BEEN IN THEIR BODIES SINCE BEFORE
BIRTH, AND ARE MORE LIKELY TO HAVE
PROBLEMS DIVIDING.
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KARYOTYPING ACTIVITY
Map each karyotype and
determine if it is male or
female?
What is its genetic disorder?
Options:
Klinfelter’s syndrome (XXY)
Edward’s syndrome (trisomy 18)
Down syndrome (trisomy 21)
Trisomy 13