Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications

Purpose: To develop a high resolution microarray based method to detect single- and multiexons gene deletions and duplications.Methods: We have developed a high-resolution comparative genomic hybridization array to detect single- and multiexon deletions and duplications in a large set of genes on a single microarray, using the NimbleGen 385K array with an exon-centric design.Results: We have successfully developed, validated, and implemented a targeted gene comparative genomic hybridization arrays for detecting single- and multiexon deletions and duplication in autosomal and X-linked disease-associated genes.Conclusion: The comparative genomic hybridization arrays can be adopted readily by clinical molecular diagnostic laboratories as a rapid, cost-effective, highly sensitive, and accurate approach for the detection of single- and multiexon deletions or duplications, particularly in cases where direct sequencing fails to identify a mutation.

[1]  David T. Okou,et al.  Microarray‐based mutation detection in the dystrophin gene , 2008, Human mutation.

[2]  A. Chinault,et al.  Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions. , 2008, Clinical chemistry.

[3]  A. Amorim,et al.  Molecular and structural analyses of maple syrup urine disease and identification of a founder mutation in a Portuguese Gypsy community. , 2008, Molecular genetics and metabolism.

[4]  Å. Borg,et al.  Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom‐in array comparative genomic hybridization (aCGH) , 2008, Human mutation.

[5]  R. Stevens,et al.  Molecular genetics of tetrahydrobiopterin‐responsive phenylalanine hydroxylase deficiency , 2008, Human mutation.

[6]  S. Sommer,et al.  A large-scale validation of dosage analysis by robust dosage-polymerase chain reaction. , 2007, Analytical biochemistry.

[7]  Chunli Yu,et al.  Characterization of an unusual deletion of the galactose-1-phosphate uridyl transferase (GALT) gene , 2006, Genetics in Medicine.

[8]  P. Gómez-Puertas,et al.  Mutational spectrum of maple syrup urine disease in Spain , 2006, Human mutation.

[9]  M. Hegde,et al.  Detecting Mutations in the APC Gene in Familial Adenomatous Polyposis (FAP) , 2006, Current protocols in human genetics.

[10]  Thomas W Prior,et al.  Experience and strategy for the molecular testing of Duchenne muscular dystrophy. , 2005, The Journal of molecular diagnostics : JMD.

[11]  R. Andrews,et al.  Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome. , 2005, American journal of human genetics.

[12]  Emmanuel Barillot,et al.  Analysis of array CGH data: from signal ratio to gain and loss of DNA regions , 2004, Bioinform..

[13]  N. Matsumoto,et al.  Genetics of Sotos syndrome , 2003, Current opinion in pediatrics.

[14]  A. Kasinski,et al.  Relationship of causative genetic mutations in maple syrup urine disease with their clinical expression. , 2003, Molecular genetics and metabolism.

[15]  J. Mendell,et al.  Rapid direct sequence analysis of the dystrophin gene. , 2003, American journal of human genetics.

[16]  D. Zwijnenburg,et al.  Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. , 2002, Nucleic acids research.

[17]  Milan Macek,et al.  Cystic fibrosis: A worldwide analysis of CFTR mutations—correlation with incidence data and application to screening , 2002, Human mutation.

[18]  P. Devilee,et al.  Ever since Knudson. , 2001, Trends in genetics : TIG.

[19]  J. Mendell,et al.  Diagnosis of Duchenne dystrophy by enhanced detection of small mutations , 2001, Neurology.

[20]  N. Drouot,et al.  Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments. , 2000, Cancer research.

[21]  R. Gatti,et al.  Scanning by DOVAM-S detects all unique sequence changes in blinded analyses: evidence that the scanning conditions are generic. , 2000, BioTechniques.

[22]  Jinong Feng,et al.  Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity. , 1999, BioTechniques.

[23]  D. Wenger,et al.  Characterization of the large deletion in the GALC gene found in patients with Krabbe disease. , 1995, Human molecular genetics.

[24]  D. Wenger,et al.  A large deletion together with a point mutation in the GALC gene is a common mutant allele in patients with infantile Krabbe disease. , 1995, Human molecular genetics.

[25]  J. Chuang,et al.  Molecular basis of maple syrup urine disease: novel mutations at the E1 alpha locus that impair E1(alpha 2 beta 2) assembly or decrease steady-state E1 alpha mRNA levels of branched-chain alpha-keto acid dehydrogenase complex. , 1994, American journal of human genetics.

[26]  J. Fridovich-Keil,et al.  A common mutation associated with the Duarte galactosemia allele. , 1994, American journal of human genetics.

[27]  A. Iwamatsu,et al.  Krabbe disease: isolation and characterization of a full-length cDNA for human galactocerebrosidase. , 1994, Biochemical and biophysical research communications.

[28]  M. Bobrow,et al.  Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene. , 1992, Journal of medical genetics.

[29]  J. Reichardt,et al.  Molecular basis of galactosemia: mutations and polymorphisms in the gene encoding human galactose-1-phosphate uridylyltransferase. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[30]  H. Kingston,et al.  Becker muscular dystrophy: correlation of deletion type with clinical severity. , 1990, Journal of medical genetics.

[31]  K. Robson,et al.  Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria , 1983, Nature.

[32]  H. Levy,et al.  Rennes-like variant of galactosemia: clinical and biochemical studies. , 1975, The Journal of pediatrics.

[33]  Thomas D. Schmittgen,et al.  Real-Time Quantitative PCR , 2002 .

[34]  M. Nellis,et al.  Gene preference in maple syrup urine disease. , 2001, American journal of human genetics.

[35]  B. Kerem Identification of the cystic fibrosis gene: genetic analysis , 1989 .