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Meiosis. Vocabulary. SOMATIC : Any cell except a sperm or egg AUTOSOME Any chromosome other than a sex chromosome (X or Y) GAMETE An egg or sperm. Mitosis allows asexual reproduction. Meiosis allows sexual reproduction. Parents are diploid.
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Vocabulary • SOMATIC:Any cell except a sperm or egg • AUTOSOMEAny chromosome other than a sex chromosome (X or Y) • GAMETE An egg or sperm
Meiosis allows sexual reproduction. Parents are diploid Homologous chromosomes are separated into single sets.
FEMALE • One pair (the sex chromosomes) are not identical in males. MALE Sex ratios: 106 boys: 100 girls (at birth)
Eye Color Brown, green
Meiosis separates chromosome pairs to form haploid gametes. Meiosis I: Homologous pairs are separated (as sister chromatids) into 2 cells Meiosis II: Similar to mitosis: sister chromatids are separated = 4 haploid cells.
MEIOSIS I Interphase I • Interphase is very similar to interphase in mitosis
MEIOSIS I Prophase I • Double stranded chromosomes and spindle fibers appear; • Nuclear membrane and nucleolus fade (synapsis aligns homologous chromosomes)
MEIOSIS I Metaphase I • Chromosome pairs (chromatids) line up • Spindle fibers attach to centromeres and centrioles
MEIOSIS I Anaphase I • Chromatids separate from matching pair (independent assortment occurs here)
MEIOSIS I Telophase I • Cytoplasm divides and 2 cells form • Each cell still has a diploid (2n) number
MEIOSIS II Prophase II Metaphase II Anaphase II Telophase/cytokinesis II
Meiosis II follows the same steps as mitosis • Key differences: • In interphase II, there is no replication of genetic material • When the sister chromatids separate during anaphase II, they are now haploid (1n) • After telophase II, you have 4 haploid (1n) cells with genetic variation (they are no longer identical) SUMMARY OF MEIOSIS II
Genetic Variation Independent Assortment: Homologous pairs can separate in different parental combinations. 2n possible gametes created
In humans: • 223 = 8 million possible gametes • This is without crossing over, which increases the number of distinct chromatids (exact number of chiasma determines how many different chromatids will exist) Possible Gametes
Genetic Variation Crossing Over: During synapsis (Prophase I) portions of non-sister chromatids are exchanged.
Genetic Variation Random Fertilization: Each sperm will fertilize and egg randomly 8 million possible gametes for each parent: 8,000,0002 = 64 trillion possible zygotes Without Crossing over. With it, there are even more!
CROSSING OVER • These are a pair of homologous chromosomes with genes A - E.
CROSSING OVER • These homologous chromosomes are made of 2 sister chromatids each. These are called TETRADS
Synaptonemal Complex! CROSSING OVER • The tetrads line up side by side (synapsis) in Prophase I • Segments cross over(form chiasma) and the pieces are traded.
CROSSING OVER • The sister chromatids end up with different copies of the genes.
Noticethat genes that are located close together will not separate during crossing over as much as a pair of genes that are further apart.
Frequency of Crossing Over • Measuring the frequency of crossing over tells you the distance between two genes (in map units)
With all of the variation produced in meiosis, how can parents have IDENTICAL TWINS? • How does the production of sperm differ from production of egg? What do you think?
Errors in meiosis are passed down to offspring (because they occur in sperm or eggs) • These errors can create sperm and eggs that have the wrong number or types of chromosomes Errors in Meiosis
Deletion: part of a chromosome is deleted (removed) • Duplication: part of a chromosome is repeated • Translocation: part of a chromosome is moved to another chromosome • Inversion: part of a chromosome is removed, then flipped around and reattached Types of errors
Non-disjunction • Failure of chromosomes to separate properly in meiosis • Meiosis I: homologues don’t separate • Meiosis II: Sister chromatids don’t separate
Monosomy: one parent does not give a copy of one chromosome • There is only 1 total in the child • 45 instead of 46 total chromosomes • The only monosomy that we see in humans (that is nonfatal) is Turner syndrome Types of errors
Females inherit only one X chromosome (XO), instead of XX • 1/2500 girls • 98% of fetuses with Turner Syndrome miscarry • Short stature, broad chest, webbed neck Turner syndrome
Trisomies • When one parent gives two copies of a chromosome • The child has 3 total of that chromosome (47 instead of 46 total chromosomes)
Down’s syndrome • 3 copies of chromosome 21 • Impairment of cognitive ability (avg. IQ 50, vs. 100 in rest of population) • Almond-shaped eyes • Health problems: heart failure, GERD, ear infections, sleep apnea • 1/733 births • More common with older mothers, but 80% are born to women under 35 Trisomy 21