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Meiosis; Chapter 6.2 I. Purpose of meiosis is to create a gamete that is haploid (half the normal number of chromosomes), from a diploid cell (complete set of chromosomes). Upon fertilization, a male gamete (sperm) will combine with a female gamete (egg), to produce a zygote (single fertilized cell).
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II. Phases; Divided into Meiosis I and Meiosis II
A. Prophase I; Almost like prophase of mitosis. Homologous chromosomes line up with each other, gene by gene to form a tetrad.
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During this phase, crossing over occurs.
During crossing over homologous chromosomes can actually break apart and exchange genetic material.
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Crossing over results in new allele combinations, and produces genetic variation.
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B. Metaphase I; Spindle fibers attach to centromeres.
Homologous chromosomes line up as tetrads (side by side) across the middle of the cell.
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C. Anaphase I; Homologous chromosomes separate and
C. Anaphase I; Homologous chromosomes separate and move to opposite ends of the cell. Centromeres, holding sister chromatids together, do not split.
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D. Telophase I; Spindle fibers break down, and chromosomes uncoil.
Cytoplasm divides to form two new cells. Each new cell has half the genetic info. of the original cell.
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E. Prophase II; Spindle fibers form and attach to the
E. Prophase II; Spindle fibers form and attach to the chromosomes in each new cell.
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F. Metaphase II; Chromosomes (still made of sister
F. Metaphase II; Chromosomes (still made of sister chromatids) line up along the center of the cell.
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G. Anaphase II; Centromeres of each chromosome split
G. Anaphase II; Centromeres of each chromosome split. Sister chromatides separate, and move to opposite poles.
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H. Telophase II; Nuclei reform, spindle fibers break
H. Telophase II; Nuclei reform, spindle fibers break down, and cytoplasm divides. New cells are haploid (n).
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III. Nondisjunction; The failure of homologous chromosomes
III. Nondisjunction; The failure of homologous chromosomes to separate properly during meiosis.
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A. Autosomal Trisomy- Somatic cell ends up with an extra chromosome.
1. Trisomy 21- Down Syndrome 1 in 700 live births Increased risk with older mother. By age 45, risk increases to 1 in 30. 2. Trisomy 13 - Patau Syndrome 1 in 5000 live births 3. Trisomy 18- Edwards Syndrome 1 in 10,000 live births B. Trisomy in gametes- 1. Trisomy X- metafemales 3 X chromosomes 2. Klinefelter’s Syndrome- Male with XXY combination. 3. Super males- XYY combination. C. Monosomy- zygote is missing a chromosome 1. Turner Syndrome- XO affects females 2. OY lethal to males
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