chapter 13 molecular detection of inherited diseases
TRANSCRIPT
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Chapter 13Chapter 13
Molecular Detection of Inherited Diseases
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ObjectivesObjectives
Describe Mendelian patterns of inheritance as exhibited by pedigree diagrams.
Give examples of laboratory methods designed to detect single-gene disorders.
Discuss non-Mendelian inheritance and give examples of these types of inheritance, such as mitochondrial disorders and trinucleotide repeat expansion diseases.
Show how genomic imprinting (epigenetics) can affect disease phenotype.
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Models of Disease EtiologyModels of Disease Etiology
Genetic (inherited) Environmental (somatic) Multifactorial (polygenic + somatic)
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Family History of Family History of PhenotypePhenotype is is Illustrated on a Illustrated on a PedigreePedigree Diagram Diagram
male affected male deceased male
female affected female deceased female
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Pedigree Diagrams Reveal Pedigree Diagrams Reveal Transmission PatternsTransmission Patterns
Sex-linked (X-linked recessive)
Autosomal recessive (AR)Autosomal dominant (AD)
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Transmission PatternsTransmission Patterns
AR, AD, or sex-linked patterns are observed in single-gene disorders (diseases caused by one genetic mutation).
Prediction of a transmission pattern assumes Mendelian inheritance of the mutant allele.
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Transmission PatternsTransmission Patterns
Gain of function mutations usually display a dominant phenotype.
Loss of function mutations usually display a recessive phenotype.
Dominant negative patterns are observed with loss of function in multimeric proteins.
+
+ +
+
+
- +
+
Normal phenotype
Abnormal phenotype
+
+
+
-
Homozygous (+/+)
Heterozygous (+/-)
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Autosomal Recessive (AR) Autosomal Recessive (AR) TransmissionTransmission
AR is the most frequently observed transmission pattern.
The mutant phenotype is not observed in the heterozygous (normal/mutant) state.
A mutation must be homozygous (mutant/mutant) to show the abnormal phenotype.
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Loss of HeterozygosityLoss of Heterozygosity
AR mutations also result in an abnormal phenotype in a hemizygous (mutant/deletion) state.
Loss of the normal allele, revealing the mutant allele, is called loss of heterozygosity, or LOH.
LOH results from somatic (environmental, not inherited) mutations or deletions of the normal allele.
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Examples of Molecular Detection Examples of Molecular Detection of Single Gene Disorders of Single Gene Disorders
Hemachromatosis I: overabsorption of iron from food caused by mutations in the gene for a membrane iron transporter (HFE).
Thrombophilic state caused by the Leiden mutation in the gene for coagulation factor V (F5) and/or specific mutations in the gene for coagulation factor II (F2).
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S
S
S
S
S
S
COOH
NH2
C282Ymutation
H63D andS65Cmutations
Cell membrane
Cytoplasm
2 Microglobulin
HFEGene product
Hemachromatosis Type I
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Exon 4
G->ARsa1 sites
240 bp
140 bp110 bp 30 bp
MW +/+ +/+ m/m +/m +/+ +/+
PCR primer
PCR primer
Mutation creates an Rsa1 site
(Mut) (+)
Agarose gel
HFE C282Y Detection by PCR-RFLP
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153 bp116 bp
Exon 10
G->A
67 bp
37 bp
+/+ +/m m/m MW
MnlI sites
PCR primer
PCR primer
(+)(Mut)
Mutation destroys an MnlI site
Agarose gel
Detection of Factor V Leiden (R506Q) Mutation by PCR-RFLP
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148 bp123 bp
Exon 10
G->A
PCR primer
Sequence-specific PCR primers
Longer primer ends on mutated base A and makes a larger amplicon
(Mut) (+)
Agaros gel
Detection of Factor V Leiden (R506Q) Mutation by SSP-PCR
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A
T
Mut probeFlap
A
A
Mutation present -> Cleavage
F Q
Complex formation
Fluorescence in plate well indicates presence of mutation
FCleavage
A
C
wt probeFlap
Normal sample(no cleavage)
Factor V Leiden (R506Q) Mutation Detection by INVADERTM Assay
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Few Diseases Have Simple Few Diseases Have Simple Transmission Patterns Due To: Transmission Patterns Due To:
Variable expressivity: range of phenotypes from the same genetic mutation
Genetic heterogeneity: different mutations cause the same phenotype Often observed in diseases with multiple
genetic components Incomplete penetrance: presence of mutation
but no abnormal phenotype
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Non-Mendelian Transmission Non-Mendelian Transmission PatternsPatterns
Single-gene disorders or disorders with multiple genetic components with nonclassical patterns of transmission: Gonadal mosaicism: somatic mutation in germ-line
cells (gonads) Genomic imprinting: nucleotide or histone
modifications that do not change the DNA sequence Nucleotide repeat expansion: increased allele sizes
disrupt gene function Mitochondrial inheritance: maternal inheritance of
mitochondrial genes
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Mitochondrial inheritance
Non-Mendelian Transmission Non-Mendelian Transmission PatternsPatterns
Gonadal mosaicism Nucleotide repeat expansion
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CGG(CGG)5–55
CGGCGGCGG(CGG)56–200
CGGCGGCGGCGGCGGCGG(CGG)200–2000+
Normal
Premutation (Carrier)
Full mutation (affected)
Amplification
Amplification and methylation
FMR-1
FMR-1
FMR-1
Nucleotide Repeat Expansion in Fragile Nucleotide Repeat Expansion in Fragile X Mental Retardation Gene (X Mental Retardation Gene (FMRFMR1)1)
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PCR Southern blot
Premutations can be detected by PCR.
Due to their large size, Southern blot is required to detect full mutations.
20–40(normal)
50–90(premutation)
Inactive X infemales cleaved by methylation-specific restrictionenzyme
Full mutation
Detection of Fragile X CGG Expansion Detection of Fragile X CGG Expansion Mutations by PCR and Southern BlotMutations by PCR and Southern Blot
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10–29 repeats(normal)
>40 repeatsHuntingtonDisease
Huntingtin
80–170 bp
Labeled PCR primer
Autoradiogram of polyacrylamide gel
Detection of Huntingtin Gene CAG Expansion Mutations by PCR
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Human Disorders Due to Human Disorders Due to Mitochondrial MutationsMitochondrial Mutations Kearnes Sayre syndrome (KSS) Pigmentary retinopathy, chronic progressive external
ophthalmoplegia (CPEO) Leber hereditary optic neuropathy (LHON) Mitochondrial myopathy, encephalopathy, lactic
acidosis, and stroke-like episodes (MELAS) Myoclonic epilepsy with ragged red fibers (MERRF) Deafness Neuropathy, ataxia, retinitis pigmentosa (NARP) Subacute necrotizing encephalomyelopathy with
neurogenic muscle weakness, ataxia, retinitis pigmentosa (Leigh with NARP)
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HV 1 HV 2
PL
PH1PH2MELAS
3243A>G
LHON3460G>A
MERRF8344A>G NARP
8393T>G
LHON11778G>A
LHON14484T>C
Areasdeleted in KSS
Mitochondrial Mutations Mitochondrial Mutations Associated with DiseaseAssociated with Disease
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Mitochondrial MutationsMitochondrial Mutations
Homoplasmy: all mitochondria in a cell are the same
Heteroplasmy: some mitochrondria are normal and others have mutations
The severity of the disease phenotype depends on the amount of mutant and normal mitochondria present
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551 bp206 bp345 bp
MspI U C U C U C
Agarose gel
U = Uuncut, no MspIC = Cut, with MspI
The presence of the mutationcreates an MspIrestrictionenzyme site in the amplicon.
Mutationpresent
Detection of NARP Mitochondrial Point Mutation (ATPase VI 8993 T→C or G) by
PCR-RFLP
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M M + +PvuII U C U C
16.6 kb (normal)
Deletion mutant
(Heteroplasmy)
The restriction enzyme,PvuII cuts once in the circularmitochondrial DNA.
M = Mutant+ = NormalU = Uncut, No PvuIIC = Cut with PvuII
Autoradiogram
Detection of KSS Mitochondrial Deletion Mutation by Southern Blot
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Genomic ImprintingGenomic Imprinting
Gene silencing due to methylation of C residues and other modifications.
Genomic imprinting occurs during production of egg and sperm.
The phenotypic effects of imprinting are revealed in diseases in which the maternal or paternal allele is lost (uniparental disomy/deletion).
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Example of Diseases Affected by Example of Diseases Affected by Genomic ImprintingGenomic Imprinting
Prader-Willi Syndrome: caused by regional deletion or mutation in the paternally inherited chromosome 15
Angelman Syndrome: a different disease phenotype caused by regional deletion or mutation in the maternally inherited chromosome 15
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DNA Methylation Detected by DNA Methylation Detected by Methylation Specific PCR (MSP-PCR)Methylation Specific PCR (MSP-PCR)
Bisulfite treatment converts unmethylated C residues to U.
PCR
…GTCMeGATCMeGATCMeGTG… …GTCGATCGATCGTG…
…GTCMeGATCMeGATCMeGTG… …GTUGATUGATUGTG… G CTAG CTAG CAC CTAGCTAGCACG G
Product No product
PCR primer PCR primer
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Other Methods for Detection of Other Methods for Detection of DNA MethylationDNA Methylation
Methylation-sensitive single-nucleotide primer extension
PCR-RFLP with methylation sensitive restriction enzymes
Southern blot with methylation-sensitive restriction enzymes
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Genetic Testing LimitationsGenetic Testing Limitations
Intergenic mutations in splice sites or regulatory regions may be missed by analysis of gene coding regions.
Therapeutic targets (except for gene therapy) are phenotypic.
Nonsymptomatic diagnosis where disease phenotype is not (yet) expressed may raise ethical concerns.
Most disease and normal traits are multicomponent systems.
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Multifactorial InheritanceMultifactorial Inheritance(Complex Traits)(Complex Traits)
Complex traits have no distinct inheritance pattern.
Complex traits include normal traits affected by multiple loci and/or environmental factors (height, blood pressure).
Quantitative traits are complex traits with phenotypes defined by thresholds. Obesity, BMI 27 kg/m Diabetes, fasting glucose 126 mg
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Genetic Testing ComplexitiesGenetic Testing Complexities
Variable expressivity: a single genetic mutation results in a range of phenotypes
Genetic heterogeneity: the same phenotype results from mutations in different genes (includes diseases with multiple genetic components)
Penetrance: presence of mutation without the predicted phenotype
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SummarySummary
Mendelian (AR, AD, and sex-linked) and non-Mendelian patterns of inheritance are exhibited by pedigree diagrams.
Frequently occurring point mutations are easily detected by a variety of molecular methods including PCR, PCR-RFLP, SSP-PCR, and Southern blot.
Non-Mendelian patterns of inheritance are exhibited by nucleotide repeat expansions, mitochondrial mutations, gonadal mosaicism, and genomic imprinting.
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SummarySummary
Gene silencing on methylation of C residues affects phenotype without changing the DNA sequence.
Although molecular methods are ideal for detection of DNA lesions, molecular analysis may not always be the optimal strategy for laboratory testing.