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Modes of Inheritance

This document discusses various patterns of inheritance including Mendelian and non-Mendelian inheritance. It covers autosomal dominant and recessive inheritance patterns as well as x-linked and y-linked inheritance. Specific genetic disorders are provided as examples for each inheritance pattern. Mitochondrial inheritance is also summarized which involves maternal inheritance of mitochondrial DNA and can cause various diseases.

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132 views

Modes of Inheritance

This document discusses various patterns of inheritance including Mendelian and non-Mendelian inheritance. It covers autosomal dominant and recessive inheritance patterns as well as x-linked and y-linked inheritance. Specific genetic disorders are provided as examples for each inheritance pattern. Mitochondrial inheritance is also summarized which involves maternal inheritance of mitochondrial DNA and can cause various diseases.

Uploaded by

sudhir_narang_3
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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Umm AL Qura University

PATTERNS OF
INHERITANCE
Dr Neda M Bogari
PATTERNS OF
INHERITANCE
• Definition

• Family Studies

• Pedigree drawing and Terminology

• Mendelian inheritance

• Non-Mendelian inheritance

• Mitochondrial inheritance
PATTERNS OF INHERITANCE:
DEFINITION
• Its the manner in which a particular genetic
trait or disorder is passed from one generation
to the next.

• Examples:
• Autosomal dominant,
• autosomal recessive,
• X-linked dominant,
• X-linked recessive,
• multifactorail, and
• mitochondrial inheritance.
PATTERNS OF
INHERITANCE
• The importance of studying the pattern of
inheritance of disorders within families:

– Genetic counseling: Advice to be given to


members of a family regarding the
susceptibility of their developing the disease
OR.

– Passing it on to their children.


IMPORTANCE
DEFINITION
• A pedigree is a chart of the genetic history of
family over several generations.
Standard symbols for pedigrees.
IMPORTANCE DEFINITION
• Locus: The position of a gene on a chromosome.
• Allele: one of several alternative form of a gene
at a given gene locus.
• Genotype: refers to an individual’s genes.
• Phenotype: refers to an individual’s physical
appearance.
• Heterozygous: having two different alleles at a
given gene locus.
• Homozygous: having identical alleles at a given
gene locus.
Genotype
• the gene types a person inherited
Phenotype
• the physical (& behavioral)
characteristics an individual displays
Alleles
Quiet! I’ll speak
for both of us! I’ll have to be
in charge now!

Dominant Normal Recessive Damaged


Allele Allele Allele Allele
MENDELIAN DISORDERS
• Austrian botanist Gregor
Mendel (1822-84)

• More than 11,000


Mendelian (monogenic)
disorders have been
revealed

• OMIM (Online Mendelian


Inheritance in Man)
database
MENDELIAN
INHERITANCE
Autosomal inheritance:

• Dominant.

• Recessive.
Sex-linked inheritance:

• Dominant.

• Recessive.
Autosomal Inheritance
I’ll have to be
Quiet! I’ll speak in charge
for both of us! now!

Dominant Normal RecessiveDamaged


Allele Allele Allele Allele
AUTOSOMAL DOMINANT
INHERITANCE
• Both male and female are affected

• The disease is observe in multiple generations

• Transmission of the disease can be from both sexes

• Mutation in only one allele is enough to express the


disease

• Vertical transmission

• The offspring have 50% chance to have the disease


AUTOSOMAL DOMINANT
DISORDER
Affected Normal
Father Mother

Affected Normal Affected Normal


Daughter Son Son Daughter
• Punnett`s square showing possible
gamete combinations for an
autosomal dominant allele

w w

W Ww Ww

w ww ww
AUTOSOMAL DOMINANT
DISORDERS
• Huntington disease
• Autosomal dominant
• Gene in chromosome 4p
• Adult onset of the disease
• Choreic movement disorder
• Mood disturbance
• Progressive loss of mental
activity
AUTOSOMAL DOMINANT
DISORDER
• Marfan Syndrome

• Autosomal dominant

• Gene in chromosome 15q


(Fibrillin)

• Connective tissue disorder


with characteristic skeletal,
dermatological, cardiac,
aortic, ocular and dural
malformations.
AUTOSOMAL DOMINANT
DISORDER

Achondroplasia is autosomal dominant genetic


disorder that is a common cause of dwarfism
Most Cancer Susceptibility Genes Are
Dominant With Incomplete Penetrance

Normal
Susceptible Carrier
Carrier, affected
with cancer
Sporadic cancer

 Penetrance is often incomplete


 May appear to “skip” generations
 Individuals inherit altered cancer susceptibility gene,
not cancer
Factors Affecting Penetrance

Modifier Carcinogens
genes

Response to DNA Hormonal/


damage reproductive
factors

Not everyone with an altered gene develops cancer


AUTOSOMAL DOMINANT
DISORDERS
• Variable expressivity: some individuals show more
aggressive form of the disease while other
showed a milder form of the disease.

• Reduced penetrance: is term used to indicate


that the disease some time to presenting no
abnormal clinical feature

• New mutation

• Codominance: the presence of two alleles in


heterozygous state (e.g. AB blood group)
AUTOSOMAL RECESSIVE INHERITANCE

• Both male and female are affected


• The disease is observe in only single
generation

• Both gene alleles (Heterozygous)


need to be affected in order to
express the disease
Autosomal Recessive Inheritance

Carrier Carrier
Father Mother

Normal Carrier Carrier Affected


Son Daughter Son Daughter
25% 50% chance carrier 25%
normal affected
• Punnet`s square showing possible gamete
combinations for an autosomal recessive
allele

a A

A Aa AA

a aa aA
Autosomal Recessive Inheritance

Noncarrier individual

Non-affected carrier
Affected individual

 Two germline mutations (one from each parent)


to develop disease
 Equally transmitted by men and women
Families with individuals expressing
autosomal recessive phenotypes.
AUTOSOMAL RECESSIVE INHERITANCE

• Consanguinity

• Pseudodominance is an autosomal recessive


condition appears in subsequent generations and
so therefore appears to follow an autosomal
dominant pattern.

• Locus heterogeneity: A single disorder, trait, or


pattern of traits caused by mutations in genes at
different chromosomal loci.
Genetic Heterogeneity
Chr 17 Chr 13

Mutations in
different
genes can
cause the
same disease
BRCA1 BRCA2

Hereditary breast and ovarian cancer


• Different mutations in the same gene can produce a
wide range of effects. In cystic fibrosis, for
instance, the gene that controls mucus production
can have more than 300 different mutations; some
cause severe symptoms; some, mild symptoms; and
some, no symptoms at all.
Autosomal Recessive disorder
• Galactosemia

• An infant is unable to
metabolize galactose

• Damage of the liver,


central nervous system and
various other body systems

• An infant may develop


jaundice, vomiting,
lethargy, irritability and
convulsions
Autosomal Recessive disorder

• Cystic fibrosis (CF)

• Gene localized at
chromosome 7q

• Affected children
have chronic
respiratory infection,
and malabsorpition
SEX-LINKED
INHERITANCE

 X-linked dominant

 X-linked recessive

 Y-linked
X-LINKED DOMINANT
INHERITANCE

• Mutations only in X chromosome

• Both males and females are affected

• Affected males transmit the disease to their


daughters (male to female only)

• Affected females transmit the disease to daughters


and sons
X-LINKED DOMINANT
INHERITANCE
X-LINKED DOMINANT
INHERITANCE

–
More females than males


– All daughters of affected males are affected, but no sons
– A child of an affected female has 50% risk of disease
X-LINKED RECESSIVE
INHERITANCE

• Mutations only in X chromosome

• Only males are affected

• Transmission through unaffected


females to male

• No male to male transmission


X-LINKED RECESSIVE
INHERITANCE
X-LINKED RECESSIVE
INHERITANCE

– Affects almost exclusively men


– Affected men born from carrier mother, with 50% risk of disease
– No male to male transmission
X-LINKED RECESSIVE
DISORDER
• Duchenne muscular
dystrophy (DMD)

• Affected gene on
chromosome Xp21

• Progressive weakness
and muscle wasting
Y-LINKED INHERITANCE

• Only males are


affected

• Male infertility
Y-LINKED INHERITANCE (Y)

– Affects only males


– Affected males always have affected fathers
– All sons of an affected male are affected
Y-linked gene (feature)

Hairy ears

Only males are affected


MITOCHONDRIAL
INHERITANCE
• All mitochondrial
DNA is maternally
inherited

• Mitochondrial
diseases are
myopathies,
neurological
syndrome,
cardiomyopathies

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