Literature DB >> 20642357

A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications.

Nora Urraca1, Lea Davis, Edwin H Cook, N Carolyn Schanen, Lawrence T Reiter.   

Abstract

The most common chromosomal abnormalities associated with autism are 15q11-q13 duplications. Maternally derived or inherited duplications of 15q pose a substantial risk for an autism phenotype, while paternally derived duplications may be incompletely penetrant or result in other neurodevelopmental problems. Therefore, the determination of maternal versus paternal origin of this duplication is important for early intervention therapies and for appropriate genetic counseling to the families. We adapted a previous single-reaction tube assay (high-resolution melting curve analysis) to determine the parent of origin of 15q duplications in 28 interstitial duplication 15q samples, one family and two isodicentric subjects. Our method distinguished parent origin in 92% of the independent samples as well as in the familial inherited duplication and in the two isodicentric samples. This method accurately determines parental origin of the duplicated segment and measures the dosage of these alleles in the sample. In addition, it can be performed on samples where parental DNA is not available for microsatellite analysis. The development of this single-tube assay will make it easier for genetic testing laboratories to provide parent-of-origin information and will provide important information to clinical geneticists about autism risk in these individuals.

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Year:  2010        PMID: 20642357      PMCID: PMC3064527          DOI: 10.1089/gtmb.2010.0030

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  16 in total

1.  High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.

Authors:  Nicholas J Wang; Dahai Liu; Alexander S Parokonny; N Carolyn Schanen
Journal:  Am J Hum Genet       Date:  2004-06-11       Impact factor: 11.025

2.  Meta-analysis of Early Intensive Behavioral Intervention for children with autism.

Authors:  Sigmund Eldevik; Richard P Hastings; J Carl Hughes; Erik Jahr; Svein Eikeseth; Scott Cross
Journal:  J Clin Child Adolesc Psychol       Date:  2009-05

3.  Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.

Authors:  T Kubota; J S Sutcliffe; S Aradhya; G Gillessen-Kaesbach; S L Christian; B Horsthemke; A L Beaudet; D H Ledbetter
Journal:  Am J Med Genet       Date:  1996-12-02

4.  Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders.

Authors:  Patrick F Bolton; Marijcke W M Veltman; Emma Weisblatt; Joanne R Holmes; N Simon Thomas; Sheila A Youings; Russell J Thompson; Siân E Roberts; Nicholas R Dennis; Caroline E Browne; Sally Goodson; Vanessa Moore; Josie Brown
Journal:  Psychiatr Genet       Date:  2004-09       Impact factor: 2.458

5.  Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.

Authors:  Christel Depienne; Daniel Moreno-De-Luca; Delphine Heron; Delphine Bouteiller; Aurélie Gennetier; Richard Delorme; Pauline Chaste; Jean-Pierre Siffroi; Sandra Chantot-Bastaraud; Baya Benyahia; Oriane Trouillard; Gudrun Nygren; Svenny Kopp; Maria Johansson; Maria Rastam; Lydie Burglen; Eric Leguern; Alain Verloes; Marion Leboyer; Alexis Brice; Christopher Gillberg; Catalina Betancur
Journal:  Biol Psychiatry       Date:  2009-03-17       Impact factor: 13.382

6.  Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

Authors:  S M Mann; N J Wang; D H Liu; L Wang; R A Schultz; N Dorrani; M Sigman; N C Schanen
Journal:  Hum Genet       Date:  2004-05-13       Impact factor: 4.132

Review 7.  Mechanisms of imprinting of the Prader-Willi/Angelman region.

Authors:  Bernhard Horsthemke; Joseph Wagstaff
Journal:  Am J Med Genet A       Date:  2008-08-15       Impact factor: 2.802

8.  Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Authors:  C C Glenn; S Saitoh; M T Jong; M M Filbrandt; U Surti; D J Driscoll; R D Nicholls
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

Review 9.  The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.

Authors:  Amber Hogart; David Wu; Janine M LaSalle; N Carolyn Schanen
Journal:  Neurobiol Dis       Date:  2008-09-18       Impact factor: 5.996

Review 10.  Early behavioral intervention, brain plasticity, and the prevention of autism spectrum disorder.

Authors:  Geraldine Dawson
Journal:  Dev Psychopathol       Date:  2008
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  7 in total

Review 1.  The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders.

Authors:  Anthony R Isles
Journal:  Transl Psychiatry       Date:  2022-05-21       Impact factor: 7.989

2.  Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples.

Authors:  Haley A Scoles; Nora Urraca; Samuel W Chadwick; Lawrence T Reiter; Janine M Lasalle
Journal:  Mol Autism       Date:  2011-12-12       Impact factor: 7.509

3.  Analysis of copy number variations at 15 schizophrenia-associated loci.

Authors:  Elliott Rees; James T R Walters; Lyudmila Georgieva; Anthony R Isles; Kimberly D Chambert; Alexander L Richards; Gerwyn Mahoney-Davies; Sophie E Legge; Jennifer L Moran; Steven A McCarroll; Michael C O'Donovan; Michael J Owen; George Kirov
Journal:  Br J Psychiatry       Date:  2013-12-05       Impact factor: 9.319

4.  Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

Authors:  Anthony R Isles; Andrés Ingason; Chelsea Lowther; James Walters; Micha Gawlick; Gerald Stöber; Elliott Rees; Joanna Martin; Rosie B Little; Harry Potter; Lyudmila Georgieva; Lucilla Pizzo; Norio Ozaki; Branko Aleksic; Itaru Kushima; Masashi Ikeda; Nakao Iwata; Douglas F Levinson; Pablo V Gejman; Jianxin Shi; Alan R Sanders; Jubao Duan; Joseph Willis; Sanjay Sisodiya; Gregory Costain; Thomas M Werge; Franziska Degenhardt; Ina Giegling; Dan Rujescu; Stefan J Hreidarsson; Evald Saemundsen; Joo Wook Ahn; Caroline Ogilvie; Santhosh D Girirajan; Hreinn Stefansson; Kari Stefansson; Michael C O'Donovan; Michael J Owen; Anne Bassett; George Kirov
Journal:  PLoS Genet       Date:  2016-05-06       Impact factor: 5.917

5.  A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism.

Authors:  Nora Urraca; Brian Potter; Rachel Hundley; Eniko K Pivnick; Kathryn McVicar; Ronald L Thibert; Christopher Ledbetter; Reed Chamberlain; Leticia Miravalle; Carissa L Sirois; Stormy Chamberlain; Lawrence T Reiter
Journal:  Front Genet       Date:  2016-11-25       Impact factor: 4.599

6.  A nine-month-old boy with isodicentric chromosome 15: a case report.

Authors:  Doug Ho Park; Seonggyu Lim; Eun Sook Park; Eun Geol Sim
Journal:  Ann Rehabil Med       Date:  2013-04-30

7.  The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.

Authors:  Nora Urraca; Julie Cleary; Victoria Brewer; Eniko K Pivnick; Kathryn McVicar; Ronald L Thibert; N Carolyn Schanen; Carmen Esmer; Dustin Lamport; Lawrence T Reiter
Journal:  Autism Res       Date:  2013-03-14       Impact factor: 5.216

  7 in total

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