Genetics 101 · DNA methylation analysis UBE3A gene sequencing FISH or Array/CGH /CMA DNA marker...
Transcript of Genetics 101 · DNA methylation analysis UBE3A gene sequencing FISH or Array/CGH /CMA DNA marker...
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Genetics 101
Stormy J. Chamberlain Department of Genetics and Genome Sciences, University of Connecticut Health Center
Angelman Syndrome Foundation Family Conference Phoenix, AZ July 13th, 2017
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Cell
Nucleus Chromosome
http://www.gencodys.eu/
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Neurons (brain cells)
Nucleus Chromosome 15
http://www.gencodys.eu/
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Humans have 22 pairs of chromosomes plus 2 sex chromosomes
46, XX 46, XY
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46, XY
We get one copy of each chromosome from mom and one copy from dad
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http://www.cureangelman.org/what-genetics101.html
Unlike most chromosomes, mom’s and dad’s copies of chromosome 15 are different from one another
The chromosome 15q11-q13 region is where the UBE3A gene is located.
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http://www.cureangelman.org/what-genetics101.html
In neurons, UBE3A is produced from mom’s copy, but not dad’s
In nearly every other cell type, UBE3A is produced from both mom’s and dad’s copies
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Genes in the chromosome 15q11-q13 region
PAT
MAT
Imprinting center –has a methylation imprint
* Methylation imprint ultimately determines the difference between mom’s and dad’s chromosomes 15.
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http://cureangelman.net/understanding-angelman/genetics101/
Molecular classes of AS
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Chromosomal/Genetic
Abnormality
% in AS
Deletion of maternal 15q11–q1 70%
Mutation in UBE3A gene 10
Paternal Uniparental Disomy (UPD) 5
Imprinting Defect (ID) 5
Unknown 10
Adapted from: Molecular epigenetics of Angelman syndrome (2007). M. Lalande and M. A. Calciano
Different Molecular Classes of AS
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Molecular Classes of AS
Typical/
Normal
AS
Deletion
70%
UPD
5%
Imprinting
defect
5%
UBE3A
mutation
10%
UBE3A
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Why do we want to know what type of AS a child has?
Credit: Dr. Charlie Williams
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Risk of Recurrence— What are the chances of having another child with AS?
Typical/
Normal Deletion
70%
UPD
5%
Imprinting
defect
5%
UBE3A
mutation
10% Prevalence in AS:
Risk of recurrence <<1%*
50%*
if inherited <<1%*
<1%
for most
50%
if deletion
* exceptions—translocation, germline mosaicism
<1%*
if spontaneous
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http://www.angelman.org/understanding-as/medical-info/genetic-counseling-in-angelman-syndrome/
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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DNA methylation testing
* methylation-specific PCR
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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UBE3A gene sequencing
DeMolfetta et al., BMC Med Genet. 2012 Dec 20;13:124. doi: 10.1186/1471-2350-13-124
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http://www.cureangelman.org/what-testing101.html
What do we learn from UBE3A gene sequencing
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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DNA methylation testing
* methylation-specific PCR
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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FISH—fluorescent in situ hybridization
Green = the tip of chromosome 15, which should be present in everyone Red = UBE3A gene. If missing, then the individual is deletion-positive.
http://www.cureangelman.org/what-testing101.html
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Test = patient DNA labeled with red dye
Reference DNA labeled with green dye
Less AS patient DNA = deletion
Less reference DNA = duplication
Microarray/Chromosomal Microarray/aCGH
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Microarray/Chromosomal Microarray/aCGH
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PAT
MAT
Type 1 vs Type 2
Type 1
Type 2
• There are additional breakpoints (BPs) downstream of BP3 that are used less frequently • The BPs are nearly identical DNA sequences that are repeated. Repeats = possible deletions
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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DNA marker analysis
http://www.devyser.com/genetic-testing/devyser-upd-15
AS caused by paternal UPD
mother
father
child w/AS
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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Imprinting defects
PAT
MAT
MAT
MAT
In females, both mom and dad chr15 become mom chr15 in oocytes or eggs
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Imprinting defects
PAT
MAT
MAT
MAT
If AS-IC is missing or doesn’t work, one of mom’s chr15 gets labeled as a dad chr15
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DNA methylation analysis
UBE3A gene sequencing
FISH or Array/CGH
/CMA DNA marker analysis
IC mutation analysis
AS unlikely
Deletion Imprinting
defect Paternal
UPD
IC deletion Epimutation
Normal Diagnostic of AS
UBE3A mutation
No deletion
Normal Normal Two paternal copies of chromosome 15
Normal Abnormal
Diagnostic Testing for AS
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Advanced Genetics
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DNA usually encodes RNA, which then encodes a protein
Gene expression
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PAT
MAT
Neurons
Gene expression across the chromosome 15q11-q13 region
PAT
MAT
Non-neurons
UBE3A-ATS
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UBE3A-ATS UBE3A UBE3A-ATS UBE3A
UBE3A-ATS silences paternal UBE3A
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Topotecan reduces UBE3A-ATS
PAT
MAT
AS Neurons
PAT
MAT
AS Neurons +topotecan
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Topotecan reduces UBE3A-ATS
UBE3A-ATS UBE3A UBE3A-ATS UBE3A
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Antisense oligonucleotides (ASOs) reduce UBE3A-ATS
PAT
MAT
AS Neurons
PAT
MAT
AS Neurons + ASO
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UBE3A-ATS UBE3A
*
Antisense oligonucleotides (ASOs) reduce UBE3A-ATS
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Acknowledgments
Funding Raymond and Beverly Sackler Foundation
Families who have donated samples