chapter 12: patterns of heredity & human genetics section 1: mendelian inheritance of human...
TRANSCRIPT
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Chapter 12:Patterns of Heredity & Human Genetics
Section 1: Mendelian Inheritance of Human Traits
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Making a Pedigree
• When genetic inheritance is represented by a picture, this is called a pedigree.
• Pedigrees are used by geneticists to map inheritance from generation to generation.
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• It is a diagram made of symbols that identify three things:– 1. Male or female
– 2. Individuals affected by the trait being studied
– 3. Family relationships
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Symbols of a pedigree:***need to know***
Carrier –
heterozygous individual
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Constructing and Reading a pedigree
***an inverted “v” means the married couple had twins*** (know)
****a horizontal line between a male and female with a
strike means the persons are divorced.**** (Need to
know)
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Constructing and Reading a pedigree
***Roman Numerals (I, II, III) refers to the generations.***
*Arabic numbers refers to individuals. (1, 2, 3, 4, 5, …)
321 4 5 6
1
1
2
2
3 4 5
I.
III.
II.
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Reading the pedigree…
How many generations are there?
How many children did II-1 have? II-7?
How are III-5 and III-2 related?
Who is III-2 in reference to I-2?
321 4 5
61
1
2
2
3 4 5
I.
III.
II.
7
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Types of Pedigrees
Pedigrees can be:a.) autosomal
*There is a 50/50 ratio between men and women of affected individuals.
b.) X- linked*Most of the males in the pedigree are affected.
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•*X-linked are carried by females, but not
expressed in females.
•*X-linked are expressed most often in
MALES.
•*In males, to express an X-linked
disorder, he only needs to have one
gene. (XY - heterozygous)
•*In females, to express an X-linked
disorder, she needs TWO alleles to show
the disorder. (XX – homozygous
recessive)
•Ex: Colorblindness, hemophilia,
baldness
•Facts about X-linked Disorders
*carried on the X-chromosome
Colorblindness Pedigree
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Colorblindness Tests
Test Name: Ishihara Test
Colorblind sees:
yellow square
Normal color:
yellow square &
faint brown circle
Colorblind sees:
the number 17
Normal Color sees:
the number 15
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Simple Recessive Heredity
• Most genetic disorders are caused by recessive alleles. This means the disorder is inherited when both parents have a recessive allele.
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Common Recessive Disorders
• Cystic Fibrosis (CF):– A defective protein in the plasma membrane of
cells causes thick mucus to build up in the lungs and digestive system.
– Mostly found among white Americans.
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Pedigree for Cystic Fibrosis
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• Tay-Sachs Disease:– The absence of an enzyme causes lipids to
accumulate in the tissues and nerve cells of the brain.
– blind, deaf, and unable to swallow. Muscles begin to atrophy and paralysis sets in and other neurological symptoms
– Death usually by age 4
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Pedigree for Tay-Sachs
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Simple Dominant Heredity
• Dominant disorders are inherited as Mendel’s rule of dominance predicted: Only one dominant allele has to be inherited from either parent.
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Common Dominant Traits & Disorders
• Simple Dominant Traits– 1. cleft chin– 2. unattached earlobes– 3. almond shaped eyes
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Disorders: Huntington’s Disease
• A lethal genetic disorder that causes certain areas of the brain to break down.
• Does not occur until 30-50 years of age so this is why it can be passed along.
• There is a genetic test that can test the presence of the allele…would you want to know?
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Is it Dominant or Recessive…
Dominant, only one parent has the disorder.
3
21 4
56
1
1
2
2 3
4
3
I.
III.
II.
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Is it Dominant or Recessive…
Recessive, neither parent has the disorder. Both
are heterozygous.
3
21 4
56
1
1
2
2 3
4
3
I.
III.
II.
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Chapter 12
Section 2: When Heredity Rules are Different
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Complex Patterns of Heredity
• Most traits are not simply dominant or recessive
• Incomplete dominance: when the phenotype of the heterozygous individual is in between those of the two homozygotes (homozygous dominant & homozygous recessive)
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• Red flower color (RR) is dominant
• White flower color (rr) is recessive
• Pink colored flowers (Rr)
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• Codominace: when the alleles of both homozygotes (BB or WW) are expressed equally in the heterozygous individual
– If a black chicken (BB) is crossed with a white chicken (WW), all offspring will be checkered
– Example: sickle-cell anemia
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• Sex-linked traits: when traits are controlled by genes located on sex chromosomes
• X-linked disorders: generally passed on from mother to son– The genetic abnormality is found on the X
chromosome– Females are XX, males are XY
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• If a female has a normal X, it would be dominant over the defective X
• In males, it will not be masked by a corresponding dominant allele because they have a “Y” chromosome
• Ex: hemophilia & Lesch-Nyhan syndrome
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• Y-linked disorders: only passed on from father to son
• Examples: excessive hair growth of the ears & male infertility
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• Polygenic inheritance: when a trait is controlled by many genes
• Examples: height, eye color, skin color, & blood type
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Changes in Chromosomal Numbers
• Humans have 23 pairs of chromosomes (46 total); more or less = disorder
• Autosomes: a non-sex chromosome– Known as chromosomes 1-22
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• Sex chromosomes: 23rd pair in humans that determine a person’s sex
• Example: Down’s Syndrome (trisomy 21)
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8 Environmental Factors That Can Also Influence Gene Expresssion
• 1. temperature
• 2. light
• 3. nutrition
• 4. chemicals
• 5. infectious agents
• 6. hormones
• 7. structural differences
• 8. age
*** know examples***