Literature DB >> 15827763

Diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR.

Stefano Regis1, Serena Grossi, Susanna Lualdi, Roberta Biancheri, Mirella Filocamo.   

Abstract

Duplication of the proteolipid protein gene (PLP1) is the most frequent cause of Pelizaeus-Merzbacher disease (PMD), a severe X-linked myelination disorder. We developed an assay for the detection of the PLP1 gene dosage by real-time quantitative PCR using the ABI Prism 7700 Sequence Detection System and the TaqMan chemistry. Copy number of the PLP1 gene was determined by the standard curve method using GAPDH as the reference gene. The assay was tested both on 50 normal controls and on 20 subjects whose PLP1 gene copy number was previously determined by quantitative fluorescent multiplex PCR. The procedure confirmed the expected results both on the male and female normal controls as well as on the 20 subjects previously tested. Ratios corresponding to the presence of one, two or three PLP1 gene copies, distributed in three non-overlapping ranges, were obtained by real-time PCR analysis. Subsequently, 29 DNA samples of putative PMD patients and possible female carriers, with unknown PLP1 gene dosage, were analysed. Five affected males carrying the PLP1 gene duplication and four female heterozygotes carrying three PLP1 gene copies were identified among them. The method is suitable for the identification of affected male patients and female carriers. Specific ranges are widely spaced, ensuring a correct assignment of the PLP1 gene copy number.

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Year:  2005        PMID: 15827763     DOI: 10.1007/s10048-005-0214-7

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  23 in total

1.  Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR.

Authors:  K Wilke; B Duman; J Horst
Journal:  Hum Mutat       Date:  2000-11       Impact factor: 4.878

Review 2.  Pelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same gene.

Authors:  Lynn D Hudson
Journal:  J Child Neurol       Date:  2003-09       Impact factor: 1.987

3.  Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females.

Authors:  Ken Inoue; Hitoshi Osaka; Virginia C Thurston; Joe T R Clarke; Akira Yoneyama; Lisa Rosenbarker; Thomas D Bird; M E Hodes; Lisa G Shaffer; James R Lupski
Journal:  Am J Hum Genet       Date:  2002-09-20       Impact factor: 11.025

4.  Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease.

Authors:  W H Raskind; C A Williams; L D Hudson; T D Bird
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

5.  Real time quantitative PCR.

Authors:  C A Heid; J Stevens; K J Livak; P M Williams
Journal:  Genome Res       Date:  1996-10       Impact factor: 9.043

6.  Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease.

Authors:  P J Wang; W L Hwu; W T Lee; T R Wang; Y Z Shen
Journal:  Pediatr Neurol       Date:  1997-09       Impact factor: 3.372

7.  Prenatal diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR.

Authors:  S Regis; M Filocamo; R Mazzotti; R Cusano; F Corsolini; G Bonuccelli; M Stroppiano; R Gatti
Journal:  Prenat Diagn       Date:  2001-08       Impact factor: 3.050

8.  Rapid real-time fluorescent PCR gene dosage test for the diagnosis of DNA duplications and deletions.

Authors:  C Ruiz-Ponte; L Loidi; A Vega; A Carracedo; F Barros
Journal:  Clin Chem       Date:  2000-10       Impact factor: 8.327

Review 9.  The proteolipid protein gene and myelin disorders in man and animal models.

Authors:  D A Yool; J M Edgar; P Montague; S Malcolm
Journal:  Hum Mol Genet       Date:  2000-04-12       Impact factor: 6.150

10.  A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPP.

Authors:  Christian T Thiel; Cornelia Kraus; Anita Rauch; Arif B Ekici; Bernd Rautenstrauss; André Reis
Journal:  Eur J Hum Genet       Date:  2003-02       Impact factor: 4.246

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  7 in total

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2.  Multiple cryptic splice sites can be activated by IDS point mutations generating misspliced transcripts.

Authors:  Susanna Lualdi; Maria G Pittis; Stefano Regis; Rossella Parini; Anna E Allegri; Francesca Furlan; Bruno Bembi; Mirella Filocamo
Journal:  J Mol Med (Berl)       Date:  2006-05-13       Impact factor: 4.599

3.  Different proteolipid protein mutants exhibit unique metabolic defects.

Authors:  Maik Hüttemann; Zhan Zhang; Chadwick Mullins; Denise Bessert; Icksoo Lee; Klaus-Armin Nave; Sunita Appikatla; Robert P Skoff
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4.  Cell surface associated glycohydrolases in normal and Gaucher disease fibroblasts.

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Journal:  J Inherit Metab Dis       Date:  2012-04-19       Impact factor: 4.982

5.  Expression of Plasmodium falciparum genes involved in erythrocyte invasion varies among isolates cultured directly from patients.

Authors:  Susana Nery; Anne-Marie Deans; Moses Mosobo; Kevin Marsh; J Alexandra Rowe; David J Conway
Journal:  Mol Biochem Parasitol       Date:  2006-06-22       Impact factor: 1.759

6.  Increased Plp1 gene expression leads to massive microglial cell activation and inflammation throughout the brain.

Authors:  Carrie L Tatar; Sunita Appikatla; Denise A Bessert; Ajaib S Paintlia; Inderjit Singh; Robert P Skoff
Journal:  ASN Neuro       Date:  2010-09-27       Impact factor: 4.146

7.  Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations.

Authors:  Serena Grossi; Stefano Regis; Roberta Biancheri; Matthew Mort; Susanna Lualdi; Enrico Bertini; Graziella Uziel; Odile Boespflug-Tanguy; Alessandro Simonati; Fabio Corsolini; Ercan Demir; Valentina Marchiani; Antonio Percesepe; Franco Stanzial; Andrea Rossi; Catherine Vaurs-Barrière; David N Cooper; Mirella Filocamo
Journal:  Orphanet J Rare Dis       Date:  2011-06-16       Impact factor: 4.123

  7 in total

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