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Gene ; 921: 148540, 2024 Aug 30.
Artigo em Inglês | MEDLINE | ID: mdl-38723785

RESUMO

BACKGROUND: Alpha-1 antitrypsin deficiency is an underdiagnosed genetic condition that predisposes to pulmonary complications and is mainly caused by rs28929474 (PI*Z allele) and rs17580 (PI*S allele) mutations in the SERPINA1 gene. OBJECTIVE: Development of a homogeneous genotyping test for detection of PI*S and PI*Z alleles based on the principles of allele-specific PCR and amplicon melting analysis with a fluorescent dye. METHODS: Sixty individuals, which included all possible genotypes that result from combinations of rs28929474 and rs17580 single nucleotide variants, were assayed with tailed allele-specific primers and SYBR Green dye in a real-time PCR machine. RESULTS: A clear discrimination of mutant and wild-type variants was achieved in the genetic loci that define PI*S and PI*Z alleles. Specific amplicons showed a difference of 2.0 °C in melting temperature for non-S and S variants and of 2.9 °C for non-Z and Z variants. CONCLUSIONS: The developed genotyping method is robust, fast, and easily scalable on a standard real-time PCR platform. While it overcomes the handicaps of non-homogeneous approaches, it greatly reduces genotyping costs compared with other homogeneous approaches.


Assuntos
Alelos , Benzotiazóis , Diaminas , Compostos Orgânicos , Quinolinas , Reação em Cadeia da Polimerase em Tempo Real , alfa 1-Antitripsina , alfa 1-Antitripsina/genética , Humanos , Reação em Cadeia da Polimerase em Tempo Real/métodos , Deficiência de alfa 1-Antitripsina/genética , Polimorfismo de Nucleotídeo Único , Técnicas de Genotipagem/métodos , Genótipo , Corantes Fluorescentes/química
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