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Chromosomes Homologous chromosomes: in a diploid cell, 46 chromosomes are grouped into 23 pairs of chromosomes. Homologous: similar shape and size, and carry the same genes
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MEIOSIS3.3 & 10.1
Meiosis:A reduction division of a diploid nucleus
to form four haploid nuclei.This allows for a sexual life cycle in living
organisms.
Number of Chromosomes
Description of condition
Cell Type
46 Diploid (2N) Typical body (somatic) cell
23 Haploid (N) Gamete,Egg or Sperm cell
Chromosomes
Homologous chromosomes: in a diploid cell, 46 chromosomes are grouped into 23 pairs of chromosomes.
Homologous: similar shape and size, and carry the same genes
Meiosis
Interphase I –All the chromosomes are duplicated and thus
each consists of two identical sister chromatids.
Figure 13.4
Key
Maternal set ofchromosomes (n = 3)
Paternal set ofchromosomes (n = 3)
2n = 6
Two sister chromatidsof one replicatedchromosome
Two nonsisterchromatids ina homologous pair
Pair of homologouschromosomes(one from each set)
Centromere
In Meiosis I:◦Prophase I – Each chromosome pairs with its
corresponding homologous chromosome to form a bivalent (a.k.a. tetrad)
Crossing Over occursduringprophase I, then the chromosomes condense.
Crossing Over
During crossing over there is exchange of DNA material between non-sister homologous chromatids.
This produces newcombinations ofalleles on the chromosomes of thehaploid cells.
This leads to geneticvariation.
Figure 13.11
Prophase Iof meiosis
Nonsisterchromatids
Bivalent
Chiasma,site ofcrossingover
Metaphase I
Metaphase II
Daughtercells
Recombinantchromosomes
ChiasmataA chiasma is an X-shaped knot-like
structure that forms where crossing over has occurred. ◦It holds a bivalent together for a while after the
chromosomes condense by supercoiling.
Centrosomes(with centriole pairs)
Sisterchromatids
Chiasmata
Spindle
Tetrad
Nuclearenvelope
Chromatin
Centromere(with kinetochore)
Microtubuleattached tokinetochore
Bivalents line up
Metaphaseplate
Homologouschromosomesseparate
Sister chromatidsremain attached
Pairs of homologouschromosomes split up
Chromosomes duplicateHomologous chromosomes
(red and blue) pair and exchangesegments; 2n = 6 in this example
INTERPHASE MEIOSIS I: Separates homologous chromosomes
PROPHASE I METAPHASE I ANAPHASE I
Interphase and meiosis I
Figure 13.8
After finishing Meiosis I, our results are two daughter cells with a haploid number of duplicated chromosomes.
Meiosis II
TELOPHASE I ANDCYTOKINESIS
PROPHASE II METAPHASE II ANAPHASE II TELOPHASE II ANDCYTOKINESIS
MEIOSIS II: Separates sister chromatids
Cleavagefurrow Sister chromatids
separate
Haploid daughter cellsforming
During another round of cell division, the sister chromatids finally separate;four haploid daughter cells result, containing single chromosomes
Two haploid cellsform; chromosomesare still doubleFigure 13.8
Telophase I, cytokinesis, and meiosis II
Meiosis I◦Homologous chromosomes separate◦Reduces the number of chromosomes from diploid to
haploid Meiosis II
◦Sister chromatids separate◦Produces four haploid daughter cells
Genetic Variation
Genetic Variation is increased by:◦Crossing over (during prophase I)◦(Random) Fusion of gametes◦Independent assortment
Sexual Reproduction
Fusion of gametes from different parents promotes genetic variation.◦This allows alleles from two different individuals
to be combined into one new individual.◦The combination of alleles is unlikely ever to
have existed before genetic variation.◦Genetic variation is essential for evolution of a
species.
Independent Assortment of genesOrganization/ orientation of pairs of homologous
chromosomes during metaphase is random.
Figure 13.10
Key
Maternal set ofchromosomesPaternal set ofchromosomes
Possibility 1
Two equally probable arrangements ofchromosomes at
metaphase I
Possibility 2
Metaphase II
Daughtercells
Combination 1 Combination 2 Combination 3 Combination 4
Karyotyping
Non-disjunction: “not coming apart” – when chromosomes fail to separate during Meiosis 1 or 2.
Gametes contain two copies or no copies of a particular chromosome.
Offspring have an extra or missing chromosome.
Figure 15.12a, b
Meiosis I
Nondisjunction
Meiosis II
NondisjunctionGametes
n + 1n + 1 n 1 n – 1 n + 1 n –1 n nNumber of chromosomes
Nondisjunction of homologouschromosomes in meiosis I
Nondisjunction of sisterchromatids in meiosis II
(a) (b)
Down’s Syndrome – Trisomy 21◦The person has 3 (instead of 2)
21st chromosomes
Age of parents vs. Down Syndrome
Do the DBQ on pg. 167 – 168: “Parental age and non-dsjunction”
Karyotype: a property of a cell – the number and type of chromosomes present in the nucleus.
Karyogram:picture of chromosomes arranged in pairs,according to their size and structure(banding patterns).
Chromosomal abnormalities
Trisomy 18, Trisomy 13
Turner’s Syndrome – females with only one X
Klinefelter’s Syndrome – males with XXY
Karyotyping is used for pre-natal (before birth) diagnosis of chromosome abnormalities.
Where do we get the cells for doing a karyotype?
1) amniocentesisExtract amniotic fluid,Inside are some of the
baby’s cells
Risks:◦Miscarriage 1 in 200 to
1 in 400◦Accuracy: 99.4%
2) chorionic villus sampling
Tissue sample from the placenta’s projections into the uterus wall
Risks?◦Slightly higher chance of
miscarriage than amniocentesis because it is done earlier in pregnancy.
◦Accuracy: 98%