Title: Meiosis to Mendel
1Meiosis to Mendel
- Chapter 9
- Read first few sections.
2Reproduction
- Asexual reproduction mitosis
- Produces clones genetically identical
individuals - What would happen if the environment changed?
- Genetic variability helps the population as a
whole survive changes
3WHY SEX ?
- Sexual reproduction combines the DNA from two
different individuals - A gene is a section of a chromosome that carries
instructions for a specific trait (protein) - An allele is a different version of a gene
- The greater the number of different combinations
of genes the more variation among individuals,
and the greater the chance of survival of the
species.
4Sex cell formation
- Sexually reproducing organisms need to produce
specialized reproductive cells or gametes. - Produced from germ cells in organs called gonads
- In females ovaries produce eggs or ova
- In males testes produce spermatozoa
- A mutation in one of your cells wont be passed
on unless it is in the germ line cells
5Diploid vs. Haploid
- In animals, most plants, and many other
organisms, each cell contains 2 sets of
chromosomes. - This is the diploid (2n) number of chromosomes.
- A pair of homologous chromosomes, one from each
parent. - Gametes contain only one member of each pair or
the haploid (n) number of chromosomes
6- When a sperm and egg combine in the process of
fertilization, or syngamy, a new diploid cell or
zygote is formed. - The gametes must be haploid, that is, have n
number of chromosomes. If the gametes were
diploid, every generation would have twice the
number of chromosomes. - To form haploid gametes, there needs to be a
process other than mitosis this is called
meiosis.
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8Meiosis
- This is a two part process meiosis I and
meiosis II, features TWO cell divisions. - However, the DNA is only replicated once
- Meiosis I and II both use the same four stages of
mitosis prophase, metaphase, anaphase and
telophase
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10Major differences between mitosis and meiosis
- Meiosis has two cell divisions.
- Meiosis has a step where homologous chromosomes
swap pieces - Increases genetic variation, new combos.
- In the first division, sister chromatids dont
split apart! Homologs separate instead. - In the second division, sister chromatids
separate like in mitosis.
11During prophase I the homologous chromosomes pair
up in synapsis. This is the longest phase of
meiosis. Crossing over may occur further
increasing genetic variation.
12Homologs dont hang together
- In metaphase I the tetrads migrate to the center
of the cell. - In Anaphase I the centromeres do not break and
one member of each homologous pair (2 sister
chromatids) move to opposite ends of the cell - Which homolog goes to which end of the cell
occurs at random. - Telophase occurs as in mitosis.
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15Meiosis II
- There is no replication of chromosomes between
telophase I and prophase II - Meiosis II proceeds just like mitosis during
anaphase the centromeres break and the two sister
chromatids go to opposite poles.
16With only 2 pairs of chromosomes, a gamete could
have any one of 4 different combinations
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18Cytokinesis
- Varies by which type of cell is being made
- If we are producing sperm, each of the four cells
produced by meiosis II become sperm.
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20- If we are making ova, cytokinesis is uneven and
one cell takes nearly all the cytoplasm, leaving
the other cell merely a package of discarded DNA
called a polar body. - In humans, the cell again divides unevenly, so at
the end of meiosis II we have formed one ovum
(egg) and three polar bodies. The polar bodies
disintegrate.
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22- The average woman produces one ovum every 28 days
- Males produce 300 million sperm/ day
- If less than 20 million / ml, a man is considered
infertile. - Fertilization is a group effort, but only one
sperm penetrates the ovum.
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25- Sometimes things go wrong.
- In anaphase I the separation of homologous
chromosomes is called disjunction. - When they do not separate it is called
nondisjunction and the resulting gametes contain
one too many or one too few chromosomes. - Fertilization results in a zygote with 45 or 47
chromosomes. This is an aneuploid (vs. euploid)
number of chromosomes
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27Chromosomal Abnormalities per 100,000 recognized
human pregnancies
15,000
85,000
spontaneous
abortions live births ------------------
--------------------------------------------------
------------------------------------- Trisomy A
Group 1
0
0
2
159
0 3
53
0 B Group
4
95
0 5
0
0 C Group 6-12
561
0 G group
21
350
113 22
424 0
28- Three copies of a chromosome is called trisomy
Down syndrome is trisomy 21 - A zygote with one too few chromosomes does not
usually develop. (monoploid) - Extra copies of the sex chromosomes (vs. the
autosomes) do not cause as much of a problem - XX is female in humans (male in birds)
- XY is male in humans
- XXY , XYY, XXX, XO all happen
- Plants do much better with multiple chromosomes
29 15,000
85,000
spontaneous abortions live
births sex chromosomes
XYY
4
46 XXY
4
44
XO 1350
8 XXX
21
44 Translocations
Balanced
14
164 Unbalanced
225
52 Polyploid
Triploid
1275
0 Tetraploid
450
0 Other (mosaics,
etc) 280
49 Total
7500 550
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31Genetics
- A gene is a section of DNA that codes for
- Proteins for structures such as muscles -
or for enzymes - RNA molecules like rRNA and tRNA
- Genes have sections of DNA next to them
- that control whether they get used or not
regulatory regions
32DNA is like magnetic recording tape song
information is encoded in the structure of the
tape magnetically. Many different songs are
recorded and each one can be played individually
(or not played). DNA is very long and thin like
recording tape.
DNA is like digital media also, because each song
can be specifically accessed at the beginning.
33- Each cell of an organism that reproduces sexually
has two copies of each chromosome, and therefore
has two copies of every gene one on each member
of each pair of chromosomes(exception is the Y
chromosome, which is smaller than the X). - The two versions of each gene are called alleles.
Alleles may be the same or different, depending
on the traits of the parents.
34- All the genes that are contained on all the
chromosomes of an individual make up that
individuals Genome. - The Genotype is all the genetic information the
individual has for a particular trait.
35- Not all genes are expressed.
- Those traits that are expressed can be seen
(physical traits) or measured (chemical traits)
are the individuals phenotype. - The phenotype is influenced by both the genotype
and the environment. - In diploid organisms (like us) an allele from one
parent can mask the appearance of the other. So
often genotype ? phenotype. - We can still pass on a hidden trait and see it in
our children.