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Meiosis

Meiosis. Reproduction. Mitosis produces somatic cells (body cells) Somatic cells have 46 chromosomes (23 pairs) What if somatic cells were involved in reproduction?. How do we solve this problem?. Oocyte. 46. Zygote. 92. 46. Spermatocte. I’ve got too many chromosomes!!!. Reproduction.

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Meiosis

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  1. Meiosis

  2. Reproduction • Mitosis produces somatic cells (body cells) • Somatic cells have 46 chromosomes (23 pairs) • What if somatic cells were involved in reproduction? How do we solve this problem? Oocyte 46 Zygote 92 46 Spermatocte I’ve got too many chromosomes!!!

  3. Reproduction • Mitosis produces somatic cells (body cells) • Somatic cells have 46 chromosomes (23 pairs) • What if somatic cells were involved in reproduction? Much better 23 46 23 Haploid Diploid

  4. Gametes • Haploid gametes keeps the chromosome number from doubling in each succeeding generation • Haploid gametes are produced by a special sort of cell division called meiosis • Meiosis • occurs only in reproductive organs, ovaries and testes • Purpose of meiosis is to produce sperm and egg • Spermatogenesis – Sperm production • Oogenesis – Egg cell production

  5. Summary of Meiosis • Meiosis involves 2 cell divisions • Meiosis produces 4 cells from 1 parental cell • Each of the 4 daughter cells has 23 individual chromosomes rather than 23 pairs of chromosomes • Meiosis reduces the chromosome number from diploid to haploid • Meiosis, like mitosis, is preceded by chromosome duplication • However, in meiosis the cell divides twice to form four daughter cells

  6. Meiosis I

  7. Meiosis II

  8. MEIOSIS I: Homologous chromosomes separate INTERPHASE PROPHASE I METAPHASE I ANAPHASE I Centrosomes(withcentriolepairs) Microtubules attached tokinetochore Metaphaseplate Sister chromatidsremain attached Sites of crossing over Spindle Nuclearenvelope Sisterchromatids Tetrad Centromere(with kinetochore) Homologouschromosomes separate Chromatin

  9. MEIOSIS II: Sister chromatids separate TELOPHASE IAND CYTOKINESIS TELOPHASE IIAND CYTOKINESIS PROPHASE II METAPHASE II ANAPHASE II Cleavagefurrow Sister chromatidsseparate Haploiddaughter cellsforming

  10. Genetic Variation in Meiosis • Meiosis provides for a vast amount of genetic variation • Crossing over – in prophase I, chromosomes exchange DNA • Independent Assortment – in anaphase I homologs independently separate, in anaphase II sister chromatids independently separate • Additional genetic variation is achieved through mating of non-related individuals

  11. Crossing Over

  12. Independent Assortment POSSIBILITY 1 POSSIBILITY 2 Two equally probable arrangements of chromosomes at metaphase I Metaphase II Gametes Combination 1 Combination 2 Combination 3 Combination 4

  13. Independent Assortment • The number of genetically distinct gametes that can be produced from a diploid cell is 2n • n = the number of chromosome pairs I wonder how many distinct gametes can be produced from independent assortment in humans? 223 = 8,388,608 combinations

  14. MITOSIS MEIOSIS PARENT CELL(before chromosome replication) Site ofcrossing over MEIOSIS I PROPHASE I Crossing over occurs PROPHASE Chromosomereplication Chromosomereplication Duplicatedchromosome(two sister chromatids) 2n = 4 Chromosomes align at the metaphase plate Homologous pairs line up at the equator METAPHASE I METAPHASE ANAPHASE I TELOPHASE I ANAPHASETELOPHASE Homologouschromosomesseparateduringanaphase I;sisterchromatids remain together Sister chromatidsseparate duringanaphase Haploidn = 2 Daughtercells of meiosis I 2n 2n No further chromosomal replication; sister chromatids separate during anaphase II MEIOSIS II Daughter cellsof mitosis n n n n Daughter cells of meiosis II

  15. Karyotype What does this karyotype tell you about the person? • A karyotype is a display of a persons chromosomes

  16. Errors in Meiosis • Nondisjunction occurs when either: • homologues fail to separate during anaphase I of meiosis, or  • sister chromatids fail to separate during anaphase II. • Trisomy- one extra chromosome (2n +1) • Monosomy - one missing chromosome (2n - 1)

  17. Down syndrome(trisomy 21): The result of an extra copy of chromosome 21. People with Down syndrome are 47, 21+. Down syndrome affects 1:700 children and alters the child's phenotype either moderately or severely: - characteristic facial features, short stature; heart defects - susceptibility to respiratory disease, shorter lifespan - prone to developing early Alzheimer's and leukemia - often sexually underdeveloped and sterile, usually some degree of mental retardation. - Down Syndrome is correlated with age of mother but can also be the result of nondisjunction of the father's chromosome 21.

  18. Patau syndrome (trisomy 13): serious eye, brain, circulatory defects as well as cleft palate. 1:5000 live births. Children rarely live more than a few months.

  19. Edward's syndrome (trisomy 18): almost every organ system affected 1:10,000 live births. Children with full Trisomy 18 generally do not live more than a few months.

  20. Klinefelter syndrome: 47, XXY males. Male sex organs; unusually small testes, sterile. Breast enlargement and other feminine body characteristics. Normal intelligence.

  21. 47, XYY males: Individuals are somewhat taller than average and often have below normal intelligence. At one time (~1970s), it was thought that these men were likely to be criminally aggressive, but this hypothesis has been disproven over time.

  22. Trisomy X: 47, XXX females. 1:1000 live births - healthy and fertile - usually cannot be distinguished from normal female except by karyotype

  23. Monosomy X (Turner's syndrome): 1:5000 live births; the only viable monosomy in humans - women with Turner's have only 45 chromosomes!!! XO individuals are genetically female, however, they do not mature sexually during puberty and are sterile. Short stature and normal intelligence. (98% of these fetuses die before birth)

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