Download - 10. patterns of inheritance
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Patterns of Inheritance
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Chromosome Review
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Genetics
• Study of the patterns of inheritance• Mendelian Genetics
– Gregor Mendel– Pea plant experiments
• Grow easily• Distinguishable characteristics
– Round/Wrinkly, Yellow/Green, Tall/Short
• Can control mating
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Terminology
• Allele—Alternate forms of a gene• Dominant Allele—trait that exerts its effects
whenever present– Symbolized by capitol letter (B)– Ex. Dwarfism, Huntington’s disease
• Recessive Allele—trait that is masked if a dominant trait is present– Symbolized by lower case letter (b)– Ex. Blue eyes
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Terminology
• Genotype—Genetic makeup of an organisms– Homozygous—2 alleles that are the same (BB or bb)– Heterozygous—2 different alleles (Bb)
• Phenotype—Observable characteristics– Brown eyes, brown hair, tall, short
• Generation—group of organisms born around the same time– P Generation—Parental– F1—offspring of parent, first filial generation– F2—1st generation of offspring
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Genetic TerminologyTerm Definition
GenerationsP First (parental) generationF1 children (Latin filii) of
generation PF2 children of generation F1
Chromosomes and Geneschromosome macromolecules found in
cells, consisting of DNA, protein and RNA
gene the unit of heredity of a living organism
locus specific location of a gene, DNA sequence, or position on a chromosome
allele one of a number of alternative forms of the same gene or genetic locus
Term Definition
Dominant and recessivedominant allele an allele that is always expressed if presentrecessive allele an allele that is only expressed if the dominant
allele is not present
Genotypes and Phenotypes genotype the genetic makeup of a cell, an organism, or
an individual homozygous contains two of the same allele of a gene
heterozygous contains two different alleles of a gene
phenotype an organism's observable characteristics or traits
true breeding pure-bred, is an organism that always passes down a certain phenotypic trait to its offspring
wild type most common phenotype in naturemutant physical or genetic difference from a mutation
in a gene
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Tracking Inheritance
• Monohybrid Cross—Mating between individuals that are BOTH heterozygous
• Dihybrid Cross—Mating between individuals that are heterozygous for 2 traits (genes)
• Punnett Square—diagram showing genotypes in a monohybrid cross– Test cross—a Punnett square done to figure out the
genotype of an unknown• Always use a homozygous recessive individual with
unknown
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Mal
e pa
rent
Female parent
Yy
Yy
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Y y
Female gametes (1:1)
Y
y
YY
Yy yy
Yy
Genotypic ratio 1:2:1 (1 YY: 2 Yy: 1 yy)Phenotypic ratio 3:1 (3 yellow: 1 green)
Mal
e ga
met
es (1
:1)
Monohybrid Cross
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y y
Y
y
Y
Mal
e ga
met
es
y
Y
y
y
Mal
e ga
met
es
y
If plant is homozygous dominant (YY):
YY
Female gametes
Yellow seeds (Yy): 100% chanceYy
Yy
Yy
Yy
yy
If plant is heterozygous (Yy):
Yy
Female gametes
Yellow seeds (Yy): 50% chanceGreen seeds (yy): 50% chance
Yy yy
yyYy
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Law of Segregation
• Two alleles of each gene are packed into separate gametes– Alleles move apart during meiosis– Occurs during meiosis 1—Metaphase
• Homologous chromosome move to opposite ends of poles
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Law of SegregationEvery individual contains a pair of alleles for each particular trait which segregate or separate during cell division (assuming diploidy) for any particular trait and that each parent passes a randomly selected copy (allele) to its offspring.
Gametes will be paired randomly with gametes from the other parent.
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Example1. P generation2. F1 generation3. F2 generation
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Genetics Problem
The ability to curl your tongue up on the sides (T, tongue rolling) is dominant to not being able to roll your tongue. A woman who can roll her tongue marries a man who cannot. Their first child has his father’s phenotype. What are the genotypes of the mother, father, and child? What is the probability that their second child will be a tongue roller?
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Law of Independent Assortment
• The segregation of alleles of one gene does not influence the alleles for another gene– Alleles are RANDOMLY packaged in gametes
• Since we have SO MANY genes, can’t keep doing punnett square.– Use Product Rule—The chance that 2 independent
events will both occur = the product of individual chances that each event will occur
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Product Rule
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Law of Independant Assortment
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About 70% of Americans perceive a bitter taste from the chemical phenylthiocarbamide (PTC). The ability to taste this chemical results from a dominant allele (T) and not being able to taste PTC is the result of having two recessive alleles (t). Albinism is also a single locus trait with normal pigment being dominant (A) and the lack of pigment being recessive (a). A normally pigmented woman who cannot taste PTC has a father who is an albino taster. She marries a homozygous, normally pigmented man who is a taster but who has a mother that does not taste PTC. What percentage of the children will be albinos? What percentage of the children will be non-taster of PTC?
Law of Independent Assortment and Dihybrid Crosses
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Recessive Disorders
• Recessive Disorder—disorder is ONLY expressed when both alleles are recessive– Can be “carried”– Heterozygous individuals
can carry gene but not express disease
Dd Hearing carrier father
Dd Hearing carrier mother
D d
D DDHearing
DdHearing (carrier)
d Dd Hearing (carrier)
dd Deaf
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Recessive Disorders
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Dominant Disorders
• Dominant Disorder– Condition is expressed when
an individual has at least one dominant allele
Achondroplasia
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Autosomal DisordersDisorder Likelihood Symptoms
Recessive DisordersAlbinism approximately 1
in 17,000Most people with albinism appear white or very pale. Because individuals with albinism have skin that entirely lacks melanin, their skin can burn more easily from overexposure
Galactosemia approximately 1 in 60,000 (Caucasians)
In galactosemic patients, galactitol accumulates in body tissues. This can result in an enlarged liver, cirrhosis, renal failure, cataracts, brain damage, and ovarian failure. Without treatment, mortality in infants with galactosemia is about 75%.
Phenylketonuria (PKU)
approximately 1 in 15,000 (US)
Abnormally high levels of phenylalanine accumulate in the blood and are toxic to the brain. Complications intellectual disability, brain function abnormalities, mood disorders, irregular motor functioning, and behavioral problems.
Sickle-cell disease approximately 1 in 5,000 (US)
Sickle-cell disease may lead to various acute and chronic complications, several of which have a high mortality rate. Sickle-cell anaemia can lead to various complications, including: increased risk of infection, stroke, and chronic pain.
Tay–Sachs disease approximately 1 in 3,500 (Ashkenazi Jews)
Tay–Sachs disease is typically first noticed in infants around 6 months old displaying an abnormally strong response to sudden noises or other stimulus, known as the “startle response.” There may also be listlessness or muscle stiffness (hypertonia).
Dominant DisordersAlzheimer’s disease unknown dementia; memory loss and mental decay; not all cases are the result of genetics
Huntington’s disease approximately 5–10 in 100,000
a neurodegenerative genetic disorder that affects muscle coordination and leads to cognitive decline and behavioral symptoms. It typically becomes noticeable in mid-adult life.
Hypercholesterolemia unknown the presence of high levels of cholesterol in the blood; can lead to atherosclerosis and other heart problems; can be caused by genetics or lifestyle
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Variations on Mendel’s Laws
• Incomplete Dominance– Individual who is
heterozygous show intermediated phenotype
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Variations on Mendel’s Laws
• Pleiotropy – One gene has many
effects
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Variations on Mendel’s Laws
• Pleiotropy – One gene has many
effects
Sickle-cells can cause many problems in a person’s life, including organ damage, chronic illness, and pain.
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Variations on Mendel’s Laws
Polygenic Inheritance—Many genes control one phenotype
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Variations on Mendel’s Laws
Polygenic Inheritance—Many genes control one phenotype
Read more here: http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.0000069
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Sex Linked Genes
• Sex Determination– Female – XX– Male - XY
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Sex Linked Genes
• Can be carried on either X or Y chromosome– More common on X chromosome
• Affect more males than females
XAXa XAYFemale Male
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Sex Chromosomes and Sex Linked Genes
• Eye color in fruit flies
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X-Linked DisordersDisorder Genetics Characteristics
X-Linked Recessive InheritanceDuchenne muscular dystrophy mutation in the dystrophin gene early life muscle degeneration and eventual death
Fragile X syndrome expansion of the CGG trinucleotide repeat on the X chromosome
most widespread single-gene cause of autism and inherited cause of intellectual disability, especially among boys
Hemophilia A mutant allele; ~70% of the time it is an X-linked recessive trait, but ~30% of cases arise from mutations
deficiency in clotting factor VIII, which causes increased bleeding and usually affects males
Red–green color blindness absence or mutation of the genes for red or green color receptors
difficulty with discriminating red and green hues
Rett syndrome mutations in the gene MECP2 located on the X chromosome
typically have no verbal skills, and about 50% of individuals affected do not walk. Scoliosis, growth failure, and constipation are very common and can be problematic.
X-Linked Dominant Inheritance Hypertrichosis unknown abnormal amount of hair growth over the bodyX-linked hypophosphatemia mutation in the PHEX gene
sequence (Xp.22) and subsequent inactivity of the PHEX protein
It can cause bone deformity including short stature and genu varum (bow leggedness).
Retinitis pigmentosa (some forms)
unknown degenerative eye disease that causes severe vision impairment and often blindness