chapter 15 chromosomes - mcccblinderl/documents/ch15chromosomes.pdf · chapter 15 chromosomes . the...
TRANSCRIPT
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Chapter 15 Chromosomes
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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 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
ovaries female
SRY discovered in 1990
Y chromosome has ~78 genes
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Chromosome theory of inheritance
• Genes located on chromosomes = gene locus
• Thomas Morgan
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• Drosophila
– 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+
on
X chromosome
Sex-linked gene!
Genotype? ww, w+w w+w+
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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
Cross f1 females with f1 males
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f1 Xw+ Xw X Xw+ Y
f2
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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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No green photoreceptors
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Example: colorblindness is X-linked
• 1/1O males
• 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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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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FYI
• Barr body testing was introduced in the 1966 Olympic games, in an effort to detect male athletes trying to "pass" as females, to gain a competitive advantage
.
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• Genes on this X are not expressed
• Lyon hypothesis
– Females mosaics for X-linked traits
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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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Chromosomal abnormalities
• Disjunction anaphase of meiosis
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If chromosome do not disjoin
• Non-disjunction
– Meiotic spindle error
– Gametes ?
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Fertilization (human)
Aneuploidy – abnormal number of chromosomes
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• Nondisjunction anaphase I
• Nondisjunction anaphaseII
• Fertilization animation at Learn Genetics
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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
Single crease in the palm of the hand
Small ears
Small mouth
Upward slanting eyes
Wide, short hands, short fingers
White spots on eye
Physical development is often slower than normal.
Delayed mental and social development.
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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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Chromosome 6p25.1 deletion and 7q21.13 duplication This is Hayes. He was born in July 2007 with a rare chromosome disorder
Chromosome 13 deletion This is a story of Maya who has a chromosome abnormality. She has a gross motor delay in which she isn't walking or crawling
22q13 deletion syndrome – Insulin treatment. The family of a little child born with a deletion of the 22q13 region of his chromosome 22
Chromosome 16 Deletion Ace's Story
Chromosome 15q Duplication Syndrome - Cody's Poem
Chromosome 12 deletion along with an inversion (in the long arm) of chromosome 12
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Inheritance of mitochondrial DNA and chloroplast DNA (plants)
• Extranuclear
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• Maternal inheritance (cytoplasm)
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