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Advanced Biology Chapter 13 Genetic Disorders
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Autosomes – 22 perfectly matched chromosomes. #s 1-22
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Sex Chromosomes – 23 rd pair XX = Female XY = Male
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Monosomic – Lost one copy of a chromosome Usually fatal, especially if on an autosome
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Trisomic – Extra chromosome 13, 15, 18 can have an extra and survive for a short time 21, 22 can survive into adulthood
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Down Syndrome – Trisomy 21 Extra copy of the 21 st chromosome
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Primary Nondisjunction – Failure of chromosomes to separate during Meiosis
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Failure to separate is correlated to age: >20 – 1:1700 births 20-30 – 1:1400 30-35 – 1:750 35-45 – 1:16
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Barr Body – One of the X chromosomes is inactivated
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Y Chromsome – Possesses some active genes, contains features associated with maleness Contains 78 genes
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NONDISJUNCTION IN SEX CHROMOMSOMES Triple X syndrome - XXX One functional X, two Barr Bodies Female is sterile but normal in other respects
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NONDISJUNCTION IN SEX CHROMOMSOMES Klinefelter Syndrome – XXY Sterile Male Has many female characteristics May have diminished mental capacity 1:500
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NONDISJUNCTION IN SEX CHROMOMSOMES Turner Syndrome – XO Sterile Female Short in stature, webbed neck Sex organs never fully mature Low mental abilities 1:5,000
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NONDISJUNCTION IN SEX CHROMOMSOMES Nonviable – OY Fails to develop Humans cannot survive without the genes on the X chromosome
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Multiple alleles – Some traits possess multiple alleles for that specific trait Blood types.
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GENETIC DISORDERS Cystic Fibrosis Autosomal Occurs mainly in the white population 1:20 carry the allele 1:1800 are homozygous recessive
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GENETIC DISORDERS A malfunction in a channel protein causes a thick mucus to be produced in the lungs Can also affect ducts in the pancreas Most affected individuals die in their teens
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GENETIC DISORDERS Sickle Cell Anemia Autosomal Recessive Occurs more frequently in the black pop. 1:1600
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GENETIC DISORDERS Hemoglobin is defective; doesn’t carry enough Oxygen
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GENETIC DISORDERS Phenylketonuria (PKU) Autosomal recessive 1:15,000
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GENETIC DISORDERS Inability to breakdown phenylalanine (aa) Can be controlled by nutrition
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GENETIC DISORDERS Tay-Sachs Disease Autosomal Recessive 1:3600 if of Jewish decent 1:300,000 in U.S
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GENETIC DISORDERS Affected individuals lack an enzyme that breaks down gangliosides in the brain These accumulate in the lysosome and burst Resulting in the destruction of brain cells
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GENETIC DISORDERS Sex-linked recessive Inability of blood to clot Missing a clotting factor
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GENETIC DISORDERS Huntington’s Disease DOMINANT 1:10,000 Gene gets turned on in middle age
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GENETIC DISORDERS Deterioration of brain cells due to the inhibition of brain cell metabolism
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GENETIC DISORDERS High risk pregnancies Parents who are: –Heterozygous for a disease –Older OR have a family history
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GENETIC COUNSELING Ultrasound – position of fetus Amniocentesis Withdraw fluid containing fetal cells
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GENETIC COUNSELING Chorionic Villi Sampling Take a sample of placental tissue
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GENE THERAPY Gene Transfer Therapy 1 st done in 1990 2 Girls had a rare blood disorder due to a defective gene Scientists isolated working copies of the gene
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GENE THERAPY Introduced them into bone marrow cells taken from each girl Gene modified bone marrow cells were allowed to proliferate (make more) Injected back into body Both girls healthy
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GENE THERAPY Use of vectors (1995) Attach gene to a virus – adenovirus (cold) Like a piggyback ride Tried it with mice and the cf gene
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GENE THERAPY Worked, tried it with humans Worked for awhile, but eventually immune system attacked virus Caused the loss of the good gene
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GENE THERAPY Problems with the vector: –Adenovirus elicits a strong immune response (everyone has had a cold) –Adenovirus can produced a severe immune reaction and be fatal
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GENE THERAPY Problems with the vector: –Adenovirus inserts its DNA into cell at a random location causing mutations
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GENE THERAPY Few years later, found new vector Use Parovirus called Adeno- Associated Virus (AAV) Has only two genes and needs the adenovirus to replicate
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GENE THERAPY Scientists removed the two genes and insert human genes in their place to take them into the cell Does not cause the problems that the adenovirus did
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GENE THERAPY In 1999, AAV cured anemia in rhesus monkeys. Also cured dogs of retinal degeneration In 2000 first human trial
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