chapter 15 chromosomes - mcccblinderl/documents/ch15chromosomespost.pdf · chapter 15 chromosomes ....
TRANSCRIPT
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Chapter 15 Chromosomes
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Chromosome theory of inheritance
• Genes located on chromosomes = gene locus
• Thomas Hunt Morgan, Columbia Univ. “Fly room”
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• Drosophila
– 100s of offspring
– 2n = 8
• 3 prs autosomes
• X and Y sex chromosomes
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Bithorax Wildtype White eye
Wingless eyeless
Wildtype = normal Mutant = abnormal
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Drosophila genetics
White eye allele = w
Wildtype allele = w+
gene locus on
X chromosome
Sex-linked!
Genotype? ww, w+w w+w+
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Chromosome with white gene
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Sex-linked genes
Cross a red female with a white male (pg. 288)
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Xw+ Xw+ X Xw Y
Punnett square results
Cross f1 females with f1 males
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f1 Xw+ Xw X Xw+ Y
f2
Some genes are located on the X chromosome
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The chromosomal basis of sex
In humans, Y chromosome determines sex
XX X XY
Gametes?
p(son)
p (daughter)
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Humans have an X/Y system
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Development <2 months gestation – embryo has rudimentary
gonads
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2 mos. SRY gene on Y chromosome active
-> testes develop
-> testosterone
-> male
If no SRY
female default pathway ovaries
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X-linked genes in humans
Female genotypes Male genotypes
XCXC XCXc XcXc XC Y XcY
Terms: homozygous, heterozygous, hemizygous Concept check:
• From whom do males obtain the Y chromosome?
• From whom do females obtain the X chromosomes?
• Why are X-linked disorders more prevalent in males?
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Example: colorblindness
• 1/1O males
• Colorblindness is an X-linked trait. A man is colorblind. What % of his sons and daughters are expected to be colorblind. His wife does not carry the colorblind allele on either X chromosome.
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No green photoreceptors
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X-chromosome inactivation in females
• One X inactivated during embryonic development Barr body (see nuclear envelope)
• # in female cells? male cells?
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• Genes on this X are not expressed
• Lyon hypothesis
– Females mosaics for X-linked traits
– Allele key
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XC
Xc
• Patches of colorblind cells in retina
• Normal phenotype
Blue colorblindness is rare
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• Genotype of orange female?
• Genotype of black female?
• Genotype of orange male?
• Genotype of black male?
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Linkage Unlinked genes
-On different chromosomes -Independent assortment! Example in pea plants: color gene (Chromosome 1) shape gene (Chromosome 7) Example in humans: Blood type (Chromosome 9) Lactose intolerance (Chromosome 2)
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Linked Genes -on same chromosome -do not assort independently
Example humans: Freckles (Chromosome 16) Red hair (Chromosome 16)
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Drosophila
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Genetic recombination of linked genes Crossing over
Meiosis
Non-sister chromatids of homologous chromosomes
25% of each
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Crossing over results in recombinants
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Chromosomal abnormalities
• Disjunction anaphase of meiosis
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If chromosome do not disjoin
• Non-disjunction
– Meiotic spindle error
– Sister chromatids do not separate in Anaphase II
– Gametes ?
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Fertilization (human)
Aneuploidy – abnormal number of chromosomes
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1. Monosomy (2n-1)
Ex. Turner syndrome 45, X 1/5,000 births
Only viable monosomy in humans
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Short stature Lymphadema of the hands and feet Broad chest Low hairline Low-set ears Reproductive sterility Rudimentary ovaries gonadal streak absence of a menstrual period Increased weight, obesity Shield shaped thorax of heart Shortened hand bones Small fingernails Characteristic facial features Webbed neck Aorta abnormalities Poor breast development Horseshoe kidney Visual impairments Ear infections and hearing loss High waist-to-hip ratio (the hips are not much bigger than the waist) Attention Deficit/Hyperactivity Disorder Nonverbal Learning Disability (problems with math, social skills and spatial relations)
Possible symptoms
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2. Trisomy (2n+1)
Ex. Trisomy 21 (Down syndrome) 1/700 births
Higher risk in women > 35
Abnormal meiosis
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Possible symptoms Common physical signs include: Excess skin at the nape of the neck Flattened nose Separated joints between the bones of the skull (sutures) Single crease in the palm of the hand Small ears Small mouth Upward slanting eyes Wide, short hands with short fingers White spots on the colored part of the eye (Brushfield spots) Physical development is often slower than normal. Most children with Down syndrome never reach their average adult height. Children may also have delayed mental and social development. Common problems may include: Impulsive behavior Poor judgment Short attention span Slow learning
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• Nondisjunction anaphase I
• Nondisjunction anaphaseII
• Fertilization animation at Learn Genetics
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Chromosome structure abnormalities
1. Deletion – fragment lost
2. Duplication – repeated fragment
3. Translocation – fragment attaches to other chromosome
4. Inversion – fragment inverts
Univ. Wisc. Genetics center tumors
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Inheritance of mitochondrial DNA and chloroplast DNA (plants)
• Extranuclear genes
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• Maternal inheritance (cytoplasm)
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