Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion  Zhengrui Xi, Lorne Zinman, Danielle Moreno, Jennifer Schymick,

Slides:



Advertisements
Similar presentations
Volume 3, Issue 4, Pages (April 2013)
Advertisements

Volume 7, Issue 5, Pages (November 2016)
Serotonin Transporter Promoter Gain-of-Function Genotypes Are Linked to Obsessive- Compulsive Disorder  Xian-Zhang Hu, Robert H. Lipsky, Guanshan Zhu,
Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability  Yasuyuki Miyakura,
Genome-Wide Identification and Validation of a Novel Methylation Biomarker, SDC2, for Blood-Based Detection of Colorectal Cancer  TaeJeong Oh, Nayoung.
MethySYBR, a Novel Quantitative PCR Assay for the Dual Analysis of DNA Methylation and CpG Methylation Density  Pang-Kuo Lo, Hanano Watanabe, Pi-Chun.
Volume 3, Issue 4, Pages (April 2013)
Discordance between Genetic and Epigenetic Defects in Pseudohypoparathyroidism Type 1b Revealed by Inconsistent Loss of Maternal Imprinting at GNAS1 
The DMPK Gene of Severely Affected Myotonic Dystrophy Patients Is Hypermethylated Proximal to the Largely Expanded CTG Repeat  Peter Steinbach, Dieter.
Tracy Dixon-Salazar, Jennifer L. Silhavy, Sarah E. Marsh, Carrie M
A Pyrosequencing-Based Assay for the Rapid Detection of IDH1 Mutations in Clinical Samples  Prashanth Setty, Jennifer Hammes, Thomas Rothämel, Valentina.
ATM Gene Mutations Result in Both Recessive and Dominant Expression Phenotypes of Genes and MicroRNAs  Denis A. Smirnov, Vivian G. Cheung  The American.
Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype.
Serotonin Transporter Promoter Gain-of-Function Genotypes Are Linked to Obsessive- Compulsive Disorder  Xian-Zhang Hu, Robert H. Lipsky, Guanshan Zhu,
Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal.
Qing Cheng, Cheng Cheng, Kristine R. Crews, Raul C
Volume 29, Issue 1, Pages (April 2014)
DNA Methylation Signatures within the Human Brain
A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation  Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana.
Demethylation of a nonpromoter cytosine-phosphate-guanine island in the aromatase gene may cause the aberrant up-regulation in endometriotic tissues 
Microsatellite Polymorphism in the Heme Oxygenase-1 Gene Promoter Is Associated with Susceptibility to Emphysema  Norihiro Yamada, Mutsuo Yamaya, Shoji.
Ying-Ying Yu, Ph. D. , Cui-Xiang Sun, Ph. D. , Yin-Kun Liu, Ph. D
Assessing loss of imprint methylation in sperm from subfertile men using novel methylation polymerase chain reaction Luminex analysis  Akiko Sato, M.E.,
A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene  Alexandra M. Dumitrescu,
Volume 124, Issue 3, Pages (March 2003)
Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome  Lihua Ying, Yitzhak Katz, Menachem Schlesinger,
Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta  Hirotaka Hamada, Hiroaki Okae, Hidehiro Toh,
Benjamin P. Song, Surbhi Jain, Selena Y. Lin, Quan Chen, Timothy M
Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family  Naoyuki Kariya, Yutaka Shimomura, Masaaki Ito 
Volume 7, Issue 5, Pages (November 2016)
S. Hussain Askree, Shika Dharamrup, Lawrence N. Hjelm, Bradford Coffee 
Molecular Therapy - Nucleic Acids
Shi-Ling Chen, M. D. , M. Sc. , Xiao-Yun Shi, M. D. , M. Sc
Syed Hussain Askree, Lawrence N
Imprinting at the SMPD1 Locus: Implications for Acid Sphingomyelinase–Deficient Niemann-Pick Disease  Calogera M. Simonaro, Jae-Ho Park, Efrat Eliyahu,
A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer  D.Gareth R. Evans, Elke.
Jump from Pre-mutation to Pathologic Expansion in C9orf72
Germline Epigenetic Silencing of the Tumor Suppressor Gene PTPRJ in Early-Onset Familial Colorectal Cancer  Ramprasath Venkatachalam  Gastroenterology 
Fatema Zahrani, Mohammed A. Aldahmesh, Muneera J. Alshammari, Selwa A
Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis  Jonathan Mill, Thomas Tang, Zachary Kaminsky, Tarang Khare, Simin.
A Novel Point Mutation Affecting the Tyrosine Kinase Domain of the TRKA Gene in a Family with Congenital Insensitivity to Pain with Anhidrosis  Shinichi.
Allelic Skewing of DNA Methylation Is Widespread across the Genome
A Recurrent Expansion of a Maternal Allele with 36 CAG Repeats Causes Huntington Disease in Two Sisters  Franco Laccone, Wilhelm Christian  The American.
Amplification Refractory Mutation System, a Highly Sensitive and Simple Polymerase Chain Reaction Assay, for the Detection of JAK2 V617F Mutation in Chronic.
A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome  Anja Naumann,
E.J. Hollox, J.A.L. Armour, J.C.K. Barber 
Tobacco-Smoking-Related Differential DNA Methylation: 27K Discovery and Replication  Lutz P. Breitling, Rongxi Yang, Bernhard Korn, Barbara Burwinkel,
Remco van Doorn, Willem H. Zoutman, Nelleke A. Gruis 
Danielle C. Smith, Alina Esterhuizen, Jacquie Greenberg 
Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly  N.A. Oates, J. van Vliet, D.L.
Epigenetic Control of the S100A6 (Calcyclin) Gene Expression
The human GPR109A promoter is methylated and GPR109A expression is silenced in human colon carcinoma cells. The human GPR109A promoter is methylated and.
ATM Gene Mutations Result in Both Recessive and Dominant Expression Phenotypes of Genes and MicroRNAs  Denis A. Smirnov, Vivian G. Cheung  The American.
A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation  Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana.
Custom Design of a GeXP Multiplexed Assay Used to Assess Expression Profiles of Inflammatory Gene Targets in Normal Colon, Polyp, and Tumor Tissue  Janice.
Compound Heterozygosity for Novel Splice Site Mutations in the BPAG2/COL17A1 Gene Underlies Generalized Atrophic Benign Epidermolysis Bullosa  Leena Pulkkinen,
Wook Lew  Journal of Investigative Dermatology 
Tracy Dixon-Salazar, Jennifer L. Silhavy, Sarah E. Marsh, Carrie M
Volume 78, Issue 6, Pages (September 2010)
GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome  Amy J. LaCroix, Deborah Stabley, Rebecca.
Volume 63, Issue 6, Pages (June 2003)
Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23  Emma Strong, Darci T. Butcher, Rajat Singhania,
Kit-Sing Au, Adelaide A. Hebert, E. Steve Roach, Hope Northrup 
Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype.
Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies  Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier,
CpG Methylation Analysis—Current Status of Clinical Assays and Potential Applications in Molecular Diagnostics  Antonia R. Sepulveda, Dan Jones, Shuji.
Identification of Novel pro-α2(IX) Collagen Gene Mutations in Two Families with Distinctive Oligo-Epiphyseal Forms of Multiple Epiphyseal Dysplasia  Paul.
Bradford Coffee, Fuping Zhang, Stephanie Ceman, Stephen T
Qing Cheng, Cheng Cheng, Kristine R. Crews, Raul C
K. Miura, M. Obama, K. Yun, H. Masuzaki, Y. Ikeda, S. Yoshimura, T
Presentation transcript:

Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion  Zhengrui Xi, Lorne Zinman, Danielle Moreno, Jennifer Schymick, Yan Liang, Christine Sato, Yonglan Zheng, Mahdi Ghani, Samar Dib, Julia Keith, Janice Robertson, Ekaterina Rogaeva  The American Journal of Human Genetics  Volume 92, Issue 6, Pages 981-989 (June 2013) DOI: 10.1016/j.ajhg.2013.04.017 Copyright © 2013 The American Society of Human Genetics Terms and Conditions

Figure 1 HhaI Assay (A) A schematic presentation of the genomic region around the G4C2 repeat. Two predicted CpG islands located in the sequences flanking the repeat were covered by three fragments. (B) DNA undigested and digested with HhaI was amplified for all three fragments and the resulting band intensity quantified. Only fragment #1 shows differential methylation between expansion carriers and noncarriers. (C) Samples with intermediate size alleles (24–43 repeats) were not methylated upstream of the G4C2 repeat (fragment #1). (D) Representative gel analysis of 12 ALS expansion carriers, 12 ALS noncarriers, and 12 controls (a higher methylation level was observed in expansion carriers versus noncarriers). The American Journal of Human Genetics 2013 92, 981-989DOI: (10.1016/j.ajhg.2013.04.017) Copyright © 2013 The American Society of Human Genetics Terms and Conditions

Figure 2 Correlation between HhaI Assay and the Bisulfite Sequencing Assay (A) Representative chromatograms of a sequence containing seven CpG sites for an expansion carrier and a noncarrier. (B) A scatter plot of the observed methylation ratio (HhaI assay) and number of methylated CpG sites (bisulfite sequencing) revealed a significant correlation between the two assays with blood DNA. The American Journal of Human Genetics 2013 92, 981-989DOI: (10.1016/j.ajhg.2013.04.017) Copyright © 2013 The American Society of Human Genetics Terms and Conditions

Figure 3 Methylation Results in Three Representative Families of Probands who Carry the C9orf72 Expansion All available family members were studied to compare methylation levels. Individual ID and C9orf72 genotype are shown beneath the corresponding diamond. Arabic numbers indicate the repeat number and “exp” represents the expansion allele. Age at the time of examination is shown in the upper right corner. Age of onset is indicated above the ID number. Gender of the family members is masked to protect confidentiality. Black/white inverted gel images from the HhaI assay are shown below the genotype. The individual number of methylated CpG sites is shown on the right side of the gel image beneath “BSP,” which stands for bisulfite sequencing PCR. The American Journal of Human Genetics 2013 92, 981-989DOI: (10.1016/j.ajhg.2013.04.017) Copyright © 2013 The American Society of Human Genetics Terms and Conditions

Figure 4 Relative Quantification of C9orf72 mRNA All transcripts were detected by an inventoried TaqMan gene expression assay (Hs00376619_m1) and relative expression was obtained by normalizing to three reference genes (HPRT1, UBC, and B2M). Error bars represent the standard error of the triplicate reactions. Expansion carriers were shown to have reduced C9orf72 expression compared nonexpansion carriers, whereas ID #8520 with 43 repeats had a normal C9orf72 mRNA level. Notably, gene expression is inversely related to methylation level. Number of methylated CpG site is shown beneath each sample. “BSP” stands for bisulfite sequencing PCR. The American Journal of Human Genetics 2013 92, 981-989DOI: (10.1016/j.ajhg.2013.04.017) Copyright © 2013 The American Society of Human Genetics Terms and Conditions