Chapter 9. Patterns of single-gene inheritancecourse.sdu.edu.cn/G2S/eWebEditor/uploadfile/...Basic...
Transcript of Chapter 9. Patterns of single-gene inheritancecourse.sdu.edu.cn/G2S/eWebEditor/uploadfile/...Basic...
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Chapter 4-1. Patterns of single-gene inheritance
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Outline
Pedigree
Inheritance pattern
Autosomal dominant inheritance, AD
Autosomal recessive inheritance, AR
X-linked dominant inheritance,XD
X-linked recessive inheritance,XR
Y-linked inheritance
Mitochondrial diseases
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Pedigree
Pedigree:
A diagram that describes family relationships, gender, disease status, and
other attributes.
pedigree analysis
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Basic pedigree notation
Normal male
Normal female
Affected
male
Affected
femaleX-linked carrier
carrier
mating
Consanguineous mating
proband
dead
No offspring
Fraternal twins
Identical twins
Sex unspecific
Abortion or stillborn
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How to draw a pedigree??
Ⅰ
Ⅱ
Ⅲ
1 2
32
1
4
2
1 5
A proband is an individual being studied or reported on. A proband
is usually the first affected individual in a family who brings a
genetic disorder to the attention of the medical community .
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Patterns of Single-Gene Inheritance
Autosomal dominant inheritance, AD
The gene concerned to single-gene disorder
was located on an autosome, and the
phenotype is dominant.
Types
complete dominance
incomplete dominance
irregular dominance
Codominance
delayed dominance
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Complete dominance
Definition: A phenotype expressed in the same way in
both homozygotes and heterozygote.
Genotype and Phenotype
A—mutant allele a— wildtype allele
Genotype AA Aa aa
Phenotype affected affected normal
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Characteristics of Complete Dominance
Aa aa
aa Aa
AaAa
Aa aa
Ⅰ
Ⅱ
Ⅲ
Ⅳ
1 2
21
1
1
2
2
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Affecteds usually have at least one affected
parent (vertical transmission). Exceptions: new
mutations and reduced penetrance.
A child of an affected and an unaffected individual
usually has a 50% chance of being affected (If the
disease is rare, almost all affecteds are
heterozygotes)
Affects both sexes,Transmitted by either sex
Normal children of an affected parent have only
normal offpring (as well as further descendants).
Exception: reduced penetrance.
Vertical transmission of the disease phenotype,
lack of skipped generarion.
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Example: Syndactyly type I
Symptoms Webbing between 3rd and 4th fingers
Fusion of the end bones in the 3rd and 4th fingers
Webbing between 2nd and 3rd toes
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Example: Syndactyly type I
I1
1
2
1
32 4
4 52
6
9
5
7 863
II
III
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incomplete dominance
or semidominance
Definition: The phenotype due to a heterozygous genotype is
different from the phenotype seen in both homozygous genotypes and its
severity is intermediate between them.
Genotype and Phenotype
A—mutant allele a— wildtype allele
Genotype AA Aa aa
Phenotype Severely affected Slightly affected normal
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Example: Achondroplasia ,ACH
the problem is in converting cartilage to bone (a process called ossification), particularly in the long bones of the arms and legs.
short stature (short-limbed dwarfism): short arms and legs;male131cm/femal124 cm;
enlarged head , a prominent forehead;
limited range of motion at the elbows;
short fingers a three-pronged (trident) hand due to the ring finger and middle finger diverge;
bowed legs ;
normal intelligence.
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Aa Aa
Aa Aaaa AA
Example: Achondroplasia ,ACH
I
II
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codominance
Definition: alleles that are both expressed when
they occur together in the heterozygous state.
Genotype and Phenotype
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MM NN MN
Blood group MN: located on 4q
Genotype MM MN NN
Phenotype M MN N
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Blood group ABO:
Alleles IA , IB and i located on 9q.
IA IA
IA i
IB IB
IB iGenotype
Phenotype A ABB
ii IA IB
O
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Parents’ blood type Progeny’s blood type
A×A
AB
B,O
A,B
A,O
A,B,O,AB
A,B,AB
O
A×O
A×B
A×AB
B×B
B×O
B×AB
AB×AB
O×O
O×AB
A,O
B,O
A,B,AB
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Irregular dominance
Definition: The phenotypes of some of the heterozygotes,
for some reason, do not appear as affected. It can be seen as a
skipped generation
Genotype and Phenotype
A—mutant allele a— wildtype allele
Genotype AA Aa aa
Phenotype affected normal or affected normal
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Penetranc(外显率) : In a population, the
proportion of individuals possessing a disease-causing
genotype who express the disease phenotype.
If the proportion is 100%, it is said complete penetrance;
forme fruste: an atypical and usually incomplete manifestation of a
disease
Total heterozygotes
Affected heterozygotesPenetrance = ————————————×100%
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Example : polydactyly postaxial I
1 2
1 2 3 4
3 41 2
34
1 25
I
II
III
IV
Skipped generation
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Expressivity (表现度): the variation of severity
of the disease. It refers to the extent of expression of
the disease phenoytype.
Pleiotropy (基因多效性): the phenomenon in
which a single gene contributes to multiple
phenotypic traits
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delayed dominance
Definition: The individuals who carry mutant allele
doesn’t onset until particular age.
Genotype and Phenotype
A—mutant allele a— wildtype allele
Genotype AA Aa aa
Phenotype affected Onset at particular age normal
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Huntington’s chorea
progressive chorea, rigidity, and dementia.
the age of onset was between 30 and 40 years
a damage of the nerve cells in the basal ganglia
and cerebral cortex( caudate and putamen
nucleus);
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Pedigree of HD
1 2
2 3 4 5
1
45
4 7
6
6
2
5
I
II
III
IV
1
1 2 3 8
4441
30 4246
20
9 10 11
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IT15 located on 4p16.3;(CAG)n in exon ;
n=9-34 normal
n>36,even more than 120,affected
Genomic imprinting
Anticipation: A remarkable phenomenon in
which a genetic disease appears earlier
appearance and with increased from with each
succeeding generation
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Sex-influenced dominance
Definition: A dominant expression that depends on the sex of
the individual although the traits is controlled by autosome .
Genotype and Phenotype
A—mutant allele a— wildtype allele
Genotype AA Aa aa
Phenotype affected Onset due to gender normal
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Example: baldness Symptom
For Aa, Male is affected; Female is normal.
An autosomal dominant trait is expressed in heterozygous males but not in heterozygous females. Heterozygous females are unaffected but pass this trait on to half of their sons .
autosomal alleles whose expression is modified by sex hormones
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Autosomal recessive inheritance
Definition: The gene concerned to single-gene
disorder was located on an autosome, and the
phenotype is recessive..
Genotype and Phenotype
A—wildtype allele a— mutant allele
Genotype AA Aa aa
Phenotype normal carrier affected
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Characteristics of AR pedigree
Affecteds within a single sibship (―horizontal‖
transmission)
Affected individuals are usually born to unaffected
(obligate carrier) parents – with a 1/4 probability of being
affected, 2/3 of normal offspring is probable carrier.
Increased probability of parental consanguinity
Affects either sex.
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Pedigree of AR
Ⅰ
Ⅱ
Ⅲ
1 2
2 41
1 2
3 4
Ⅳ
3
1 2
Aa Aa
Aa
Aa Aa
Aa
Aa
aa AA
aa
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The chance that both parents are carriers of a mutant
allele at the same locus is increased substantially if the
parents are related and each could have inherited the
mutant allele from a single common ancestor, a
situation called consanguinity.
Close relatives: 3 or 4 generation
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Phenylketonuria type Ⅰ
Congenital deafness type Ⅰ
Infantile severe myopia
Albinism type Ⅰ
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X-linked recessive inheritance,XR
Definition: The gene concerned to single-gene disorder was
located on the X chromosome, and the phenotype is recessive.
Genotype and Phenotype
XA—wildtype allele Xa— mutant allele
Genotype Phenotype
Male XaY affected
XAY normal
Female XAXA normal
XAXa carrier
XaXa affected
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XRY XRXr
XrY
XRXr ;
XRXR
XRXR
Ⅰ
Ⅱ
Ⅲ
1 2
1 2 3 4 5 6
1 2 3 4 5 6 7
Pedigree of XR
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Characteristics of XR Pedigree
Most affected individuals are male
Affected males result from mothers who are affected or who are carriers (have affected brothers, fathers, or maternal uncles)
Affected females have affected fathers and affected (or carrier) mothers
The sons of affected females are affected
Approximately half the sons of a carrier female should be affected
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carrier girl normal girl1 out of 4 chance
25%
1 out of 4 chance
25%
affected boy normal boy1 out of 4 chance
25%
1 out of 4 chance
25%
XR
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affected girl carrier girl affected boy normal boy1 out of 4 chance
25%
1 out of 4 chance
25%
1 out of 4 chance
25%
1 out of 4 chance
25%
carrier mother of
mutant geneaffected
father
eggs sperms
Xr = recessive mutant gene
X or Y = wild-type gene
XR
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Hemophilia A
Hemophilia, hereditary blood disease, characterized by the inability of blood to clot, or coagulate, leading to hemorrhage, or excessive bleeding, even from minor injuries.
The disease is caused by an insufficiency or absence of factor Ⅷ, that participate in blood clotting.
It is caused by a recessive allele on the X chromosome.
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Ⅰ
Ⅱ
Ⅲ
1 2
21
1 2 3 4 5
3 4
8
5 6
6
7
7
Hemophilia A
XaY
XAY XAXa
XAXA
XAXa
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Color-blindness
Can not recognize correctly red color and green color
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X-linked dominant inheritance,XD
Definition: The gene concerned to single-gene disorder was
located on the X chromosome, and the phenotype is dominant.
Genotype and Phenotype
XA—mutant allele Xa— wildtype allele
Genotype Phenotype
Male XaY normal
XAY affected
Female XAXA affected
XAXa affected
XaXa normal
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Ⅰ
Ⅱ
Ⅲ
1 2
2 41
1 2
3 4
Ⅳ
3
1 2
3 4 5
Pedigree of XD
XA XaXaY
Xa XaXAY XA Xa
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Characteristics of XD Pedigree
Affects females preferentially , but also affects males
Females often more mildly and more variably
affected
If mother is affected, recurrence risk is 50%; if father,
100% of daughters will be affected
No male to male transmission
Does not skip generations
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XD
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XD
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Vitamin D resistant Rickets
this is the most frequently encountered form of rickets
Hypophosphatemia
decreased reabsorpion of phosphate by the renal proximal
tubule
administration of high doses of vitamin D have no beneficial
effect
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Vitamin D resistant Rickets
widening of epiphyseal plates bowing of the leg
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Y-linked inheritance
Disease genes are on Y chromosome
Affects males only
All sons of affected father are affected
TDF or SRY
AZF( azoospermia factor)
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Ⅰ
Ⅱ
Ⅲ
1 2
21
1 2 3 4 5
3 5
6
4
Pedigree of Y-linked inheritance
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Mitochondrial diseases
Disease genes are on mitochondria
Maternal inheritance
Ⅰ
Ⅱ
Ⅲ
1 2
21
1 2 3 4 5
3 5
6
4
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heterogeneity
Same diseases caused by different genetic factors;
Locus heterogeneity——A single disorder, trait, or pattern
of traits caused by mutations in genes at different
chromosomal loci .
Allelic heterogeneity——A single disorder, trait, or pattern
of traits caused by different mutations within a gene .
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Example of heterogeneity
Congenital deafness:
AD
AR (more than 100 loci)
XR
Retinitis pigmentosa
12 autosomal dominant forms
5 autosomal recessive forms
3 X-linked forms
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I
II
III
1 2
1 2 3 4 5 6
321 4 5 6 7XR
aaaa aaBB
AAbb
AaBb
Aa
aaAa/AA
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phenocopy
A mimic of a phenotype that is
usually determined by a specific
genotype , produced instead by
the interaction of some
environmental factor with a
normal genotype.
phenotype (generally referring to
a single trait), under a particular
environmental condition, is
identical to phenotype determined
by the genotype. Chocolate-colored male Himalayan Rabbi
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Pedigree Analysis
Dominant or recessive ?
Sex difference?
Genotype analysis
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Ⅰ
Ⅱ
Ⅳ
1 2
1
1
1
2 3
3
4
2
Ⅲ
AD: Irregular dominance
aaAa
Aa
Aa aa
Aa
Aa
Aa aa
aaAa
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Ⅰ
Ⅱ
Ⅲ
1 2
21
1 2 3
3 5
5
4
XR
4
XAY XAXa
XAXa
XaYXAY
XAXa
XAXA
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Ⅰ
Ⅱ
Ⅲ
1 2
21
1 2 3
3 6
4
54
AD
Aa aa
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Ⅰ
Ⅱ
Ⅲ
1 2
1 4
1
1
3
32
3
2
2
Ⅳ
AR
Aa
aa
Aa
Aa
AA
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Normal male is AB blood type; normal female is B blood type, and her
father is O blood type with color blind. What are the phenotype and
genotype of their offspring when the man and female married?
P IAIBXBY IBiXBXb×
gamte IAXB IAYIBXB IBY
IBXB
iXB
IBXb
iXb
F1 IAIBXBXB IAIBXBXb IAiXBXB IAiXBXb
IAIBXBY IAIBXbY IAiXBY IAiXbY
IBIBXBXB IBIBXBXb IBiXBXB IBiXBXb
IBIBXBY IBIBXbY IBiXBY IBiXbY
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