Title: Inheritance%20Patterns%20
1Inheritance Patterns Human Genetics
2(12-1) Human Males Females
- Sex chromo.s (X Y)
- Male XY
- Female XX
- Gametes
- Egg carry only X
- Sperm carry X or Y
3Key Idea
50 chance female offspring 50 chance male
offspring
4Who Discovered Sex Chromosomes?
- Thomas Morgan
- Early 1900s
- Columbia University
- Worked w/ fruit flies
5Sex Linkage
- Gene on a sex chromo.
- X-linked genes
- Y-linked genes
6Sex Linked Traits
- Most sex linked genes found on the X chromo.
- Genes on the Y chromo. are for male reproductive
organ development
7Sex Linked Genetic Problems
- In flies R red eyes, r white eyes
- Gene located on the X chromosome
X
X
X
Y
8Example 1
- White eye male mates w/ a red ho/go dominant
female - XrY x XRXR
Xr
Y
XRXr
XRY
100 red female 0 white female 100 red
male 0 white male
XR
XRXr
XRY
XR
9Example 2
- Red eye male mates w/ a red he/go female
- XRY x XRXr
XR
Y
XRXR
XRY
100 red female 0 white female 50 red
male 50 white male
XR
XRXr
XrY
Xr
10Example 3
- White eye male mates w/ a red he/go female
- XrY x XRXr
Xr
Y
XRYr
XRY
XR
50 red female 50 white female 50 red
male 50 white male
XrXr
XrY
Xr
11What would you expect from crossing 2 he/go flies?
12Morgans Results
- These characteristics are on the same chromo.,
thus they are linked together during meiosis
13Linkage Groups
- Genes located on the same chromo.s therefore
inherited together - Goes against Law of
- Indep. Assortment
14How do linked genes get unlinked?
- Crossing over
- Frequency of crossing over b/w certain genes is
used to make a chromosome map
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16Chromosome Map
- Linear sequence of genes on a chromo.
- 1 map unit 1 chance of crossing over
- Farther apart greater chance of genes to be
separated
17Which 2 genes have the highest probability of
crossing over? The lowest?
A
a
Highest A C Lowest A B
B
b
C
c
18Mutation
- Change in DNA
- Entire chromo. or a single nucleotide
- Can lead to genetic disorders or be beneficial
19Mutation Types
- Germ-cell mutation occurs in gametes
- Does not affect the organism, but can be passed
on - Somatic-cell mutation occurs in body cells
- Does affect organism is not passed on
- Lethal mutation causes death, often before birth
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21Chromosome Mutations
- Change in the structure of a chromo.
- Deletion/addition
- Inversion segment breaks off reattaches in
reverse - Translocation segment breaks off reattaches to
another chromo. - Nondisjunction failure of chromo.s to separate
during meiosis
22Nondisjunction
23Gene Mutations
- Point mutation substitution at 1 point in DNA
- Changes 1 codon
- Frame-shift mutation cause the misreading of all
codons after the mutation
24Substitution
Deletion
25(12-2) Pedigree
- Diagram showing how a trait is inherited over
several generations
Half-filled carrier
26Human Patterns of Inheritance
- Single allele trait
- Multiple allele trait
- Polygenic trait
- X-linked trait
- Sex-influenced trait
- Nondisjunction
27Single Allele Trait
- Trait controlled by a single allele of a gene
- Normal dom.-rec.
- Ex
- Huntingtons Disease (autosomal dom.)
- Cystic Fibrosis (autosomal rec.)
28Multiple Allele Trait
- 3 or more alleles of the same gene code for a
single trait - Ex ABO Blood Groups
- IA type A (dom.)
- IB type B (dom.)
- i type O (rec.)
29Blood Type Genotypes
- What are the genotypes for the following blood
types? - A
- IAIA or IAi
- B
- IBIB or IBi
- O
- ii
- AB
- IAIB
30Blood Type Problems
- A mother gives birth to a type O child. The
mother is type A blood. The 2 potential fathers
are type A (father 1) and type AB (father 2).
Whos the daddy?
31Father 1 (Type A)
IA
i
IA
A
A
i
IA
i
A
O
IA
A
A
IB
AB
B
32Polygenic Trait
- Trait thats controlled by 2 or more genes
- Most human characteristics
- Range of phenotypes
- Influenced by environment too (complex characters
environ. genes) - Exs
- Skin color
- Eye color
- Human height
33X-Linked Trait
- Trait controlled by a gene on the X chromo.
- Exs
- Colorblindness (rec.)
- Muscular dystrophy (rec.)
- Hemophilia (rec.)
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36Sex-Influenced Traits
- Presence of sex hormones influences expression of
these traits - Ex
- Pattern baldness
37Nondisjunction
- Failure of chromo.s to separate during meiosis
resulting in 1 gamete w/ too many chromo.s 1
w/ too few
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39Nondisjunction (cont.)
- Trisomy cell w/ 3 copies of a chromo.
- Monosomy cell w/ 1 copy of a chromo.
- Ex
- Down Syndrome (Tri-21)
- Klinefelters syndrome (XXY)
- Turners Syndrome (XO)
40Detecting Disorders
- Before pregnancy
- Genetic screening
- Genetic counseling
- During pregnancy
- Amniocentesis
- Chorinonic villi sampling
- After birth
- Genetic screening