Literature DB >> 21437994

Employment of single-strand conformation polymorphism analysis in screening for α-1,3 glucosyltransferase gene mutation A333V in Croatian population.

Sandra Supraha Goreta1, Sanja Dabelic, Jerka Dumic.   

Abstract

Congenital disorder of glycosylation type Ic (CDG-Ic) is caused by mutations in hALG6 gene encoding α-1,3 glucosyltransferase (NP_037471.2), an enzyme that catalyzes the addition of the first glucose residue to the growing lipid-linked oligosaccharide precursor in N-glycosylation process. The most frequent mutation in hALG6 gene causing CDG-Ic is c.998C>T that results in p.A333V substitution. Up-to-date, no CDG-Ic patient has been detected in Croatia. However, as a part of the comprehensive project undertaken with the aim to estimate the frequencies of the carriers for specific mutations and polymorphisms related to particular CDGs in Croatian population, we screened genomic DNA samples obtained from 600 healthy nonconsanguineous Croatian residents to determine the frequency of the A333V mutation. For that purpose, we established the conditions for polymerase chain reaction-based single-strand conformation polymorphism analysis that is suitable for primary screening and in population studies, especially when the initial sample volume is small or DNA quantity is limited. None of the analyzed samples carried this mutation, indicating that the frequency of the patients carrying this homozygous mutation in Croatian population would be <1 in 1.4×10(6).
© 2011 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21437994      PMCID: PMC6647718          DOI: 10.1002/jcla.20425

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  23 in total

1.  PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families.

Authors:  C Bjursell; A Erlandson; M Nordling; S Nilsson; J Wahlström; H Stibler; B Kristiansson; T Martinsson
Journal:  Hum Mutat       Date:  2000-11       Impact factor: 4.878

Review 2.  Congenital disorders of glycosylation: a review.

Authors:  Stephanie Grunewald; Gert Matthijs; Jaak Jaeken
Journal:  Pediatr Res       Date:  2002-11       Impact factor: 3.756

3.  Clinical and molecular characterization of the first adult congenital disorder of glycosylation (CDG) type Ic patient.

Authors:  Liangwu Sun; Erik A Eklund; Johan L K Van Hove; Hudson H Freeze; Janet A Thomas
Journal:  Am J Med Genet A       Date:  2005-08-15       Impact factor: 2.802

4.  A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic.

Authors:  T Imbach; P Burda; P Kuhnert; R A Wevers; M Aebi; E G Berger; T Hennet
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

5.  Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis.

Authors:  S Grünewald; T Imbach; K Huijben; M E Rubio-Gozalbo; A Verrips; J B de Klerk; H Stroink; J F de Rijk-van Andel; J L Van Hove; U Wendel; G Matthijs; T Hennet; J Jaeken; R A Wevers
Journal:  Ann Neurol       Date:  2000-06       Impact factor: 10.422

6.  Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic.

Authors:  V Westphal; C Schottstädt; T Marquardt; H H Freeze
Journal:  Mol Genet Metab       Date:  2000-07       Impact factor: 4.797

7.  A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.

Authors:  Nina Rind; Verena Schmeiser; Christian Thiel; Birgit Absmanner; Jürgen Lübbehusen; Julia Hocks; Neophytos Apeshiotis; Ekkehard Wilichowski; Ludwig Lehle; Christian Körner
Journal:  Hum Mol Genet       Date:  2010-01-15       Impact factor: 6.150

8.  Congenital disorder of glycosylation Ic in patients of Indian origin.

Authors:  J W Newell; N-S Seo; G M Enns; M McCraken; J F Mantovani; H H Freeze
Journal:  Mol Genet Metab       Date:  2003-07       Impact factor: 4.797

9.  A new capillary zone electrophoresis method for the screening of congenital disorders of glycosylation (CDG).

Authors:  Fabienne Parente; Nicholas Ah Mew; Jaak Jaeken; Brian M Gilfix
Journal:  Clin Chim Acta       Date:  2009-10-27       Impact factor: 3.786

10.  Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin.

Authors:  Hubert A Carchon; Roland Chevigné; Jean-Bernard Falmagne; Jaak Jaeken
Journal:  Clin Chem       Date:  2003-11-18       Impact factor: 8.327

View more
  2 in total

1.  Frequency Determination of α-1,3 Glucosyltransferase p.Y131H and p.F304S Polymorphisms in the Croatian Population Revealed Five Novel Single Nucleotide Polymorphisms in the hALG6 Gene.

Authors:  Sandra Supraha Goreta; Sanja Dabelic; Dinko Pavlinic; Gordan Lauc; Jerka Dumic
Journal:  Genet Test Mol Biomarkers       Date:  2011-09-07

Review 2.  Insights into complexity of congenital disorders of glycosylation.

Authors:  Sandra Supraha Goreta; Sanja Dabelic; Jerka Dumic
Journal:  Biochem Med (Zagreb)       Date:  2012       Impact factor: 2.313

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.