Literature DB >> 16319694

Rapid PCR real-time genotyping of M-Malton alpha1-antitrypsin deficiency alleles by molecular beacons.

Germano Orrù1, Gavino Faa, Sara Pillai, Luca Pilloni, Caterina Montaldo, Gesuina Pusceddu, Vincenzo Piras, Pierpaolo Coni.   

Abstract

Alpha1-Antitrypsin deficiency is an autosomal codominant inherited disorder, with increased risk of developing lung and liver disease. The large majority of subjects affected by alpha1-antitrypsin deficiency carry the PIZZ or PISZ genotypes, which can be easily detected using several molecular methods. Another pathologic allele, the M-Malton variant (also known as Mnichinan and Mcagliari), can mimic the Pi Z clinical phenotype, but this alpha1-antitrypsin deficiency variant is not easily recognizable and, therefore, seems to be more under-recognized than the Z or S alleles. We report the development of a rapid qualitative fluorescent real-time PCR assay designed for the detection of the M-Malton alpha1-antitrypsin deficiency alleles using 2 specific molecular beacons. The assay is able to detect in a single tube the homozygous as well the heterozygous genotypes. The procedure combines the great sensitivity of the polymerase chain reaction, the specificity provided by allele-specific molecular beacons, and the throughput of a multi-color fluorescence detection procedure. This technique will be useful for research and molecular diagnostic laboratories involved in the study of alpha1-antitrypsin deficiency-related diseases.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16319694     DOI: 10.1097/01.pas.0000178221.44474.b3

Source DB:  PubMed          Journal:  Diagn Mol Pathol        ISSN: 1052-9551


  8 in total

1.  Rapid and inexpensive detection of alpha1-antitrypsin deficiency-related alleles S and Z by a real-time polymerase chain reaction suitable for a large-scale population-based screening.

Authors:  Marcin P Kaczor; Marek Sanak; Andrew Szczeklik
Journal:  J Mol Diagn       Date:  2007-02       Impact factor: 5.568

2.  Rapid genotyping of alpha 1 antitrypsin deletion mutation (PI*Mmalton) using bi-directional PCR allele-specific amplification.

Authors:  Sabri Denden; Ramzi Lakhdar; Nadia Leban; Jemni Ben Chibani; Amel Haj Khelil
Journal:  Mol Biotechnol       Date:  2010-06       Impact factor: 2.695

3.  Molecular beacons: powerful tools for imaging RNA in living cells.

Authors:  Ricardo Monroy-Contreras; Luis Vaca
Journal:  J Nucleic Acids       Date:  2011-08-22

4.  Application of a diagnostic algorithm for the rare deficient variant Mmalton of alpha-1-antitrypsin deficiency: a new approach.

Authors:  Irene Belmonte; Miriam Barrecheguren; Rosa M López-Martínez; Cristina Esquinas; Esther Rodríguez; Marc Miravitlles; Francisco Rodríguez-Frías
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2016-10-11

5.  Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report.

Authors:  Sabri Denden; Michele Zorzetto; Fethi Amri; Jalel Knani; Stefania Ottaviani; Roberta Scabini; Marina Gorrini; Ilaria Ferrarotti; Ilaria Campo; Jemni Ben Chibani; Amel Haj Khelil; Maurizio Luisetti
Journal:  Orphanet J Rare Dis       Date:  2009-04-15       Impact factor: 4.123

6.  Prevalence of PI*Z and PI*S alleles of alpha-1-antitrypsin deficiency in Finland.

Authors:  Jan Häggblom; Kaisa Kettunen; Jussi Karjalainen; Markku Heliövaara; Pekka Jousilahti; Seppo Saarelainen
Journal:  Eur Clin Respir J       Date:  2015-09-24

7.  Genetic Variants Involved in Bipolar Disorder, a Rough Road Ahead.

Authors:  Germano Orrù; Mauro Giovanni Carta
Journal:  Clin Pract Epidemiol Ment Health       Date:  2018-02-28

8.  Design of FRET Probes for SNP RS1006737, Related to Mood Disorder.

Authors:  Germano Orrù; Mauro Giovanni Carta; Alessia Bramanti
Journal:  Clin Pract Epidemiol Ment Health       Date:  2018-02-28
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.