ANÁLISE MOLECULAR DO GENE RECEPTOR DE ANDRÓGENO EM PACIENTES E FAMILIARES COM SÍNDROME DA INSENSIBILIDADE AOS ANDRÓGENOS

• Ano de defesa: 2012
• Autor(a) principal: ANDRADE, Marcelo Souza de
• Orientador(a): MESQUITA, Emygdia Rosa do Rego Barros Pires Leal
• Banca de defesa: Monteiro, Silvio Gomes
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal do Maranhão
• Programa de Pós-Graduação: PROGRAMA DE PÓS-GRADUAÇÃO EM BIOTECNOLOGIA - RENORBIO/CCBS
• Departamento: Fertilização
• País: BR
• Palavras-chave em Português: Síndrome de Insensibilidade Androgênica (AIS); Gene AR - Mutação; Biologia Molecular - Técnicas
• Palavras-chave em Inglês: Androgen Insensitivity Syndrome (AIS); AR Gene - Mutation; Molecular biology - Techniques
• Área do conhecimento CNPq: CIENCIAS BIOLOGICAS::GENETICA::GENETICA HUMANA E MEDICA
• Link de acesso: http://tedebc.ufma.br:8080/jspui/handle/tede/72

Introduction. The androgen insensitivity syndrome (AIS) is a rare disease (1:20,000 to 1:64.000)-linked X chromosome, which generates a disorder of sexual differentiation of the male fetus (XY) with a spectrum of phenotypes ranging from females complete (CAIS) to a male phenotype with discrete signs of androgen insensitivity. An increasing number of mutations have been cataloged and nearly 500 mutations have been related to CAIS and 1000 to the androgen receptor gene. The AR gene is located on Xq11-12, with eight exons, about 919 amino acids. Objective. To characterize the mutations in the AR gene families in the region of the "Bico do Papagaio" in the southwestern state of Maranhao. Methodology. We used molecular biology techniques such as DNA extraction, PCR, electrophoresis, purification of PCR products and sequencing. In addition, we analyzed the clinical and hormonal characteristics of 14 patients and their families. Results. In one family (with two twin affected), we found the mutation R753X and the third molecular diagnosis of CAIS in twins described in the World. In another family, with 12 patients, was identified a new mutation in exon 8, as described P893A, protein AR. Conclusion. This work enabled the application of molecular techniques for the accurate diagnosis of AIS, genetic counseling for relatives of affected patients, and contribute to the formation of more qualified human resources, aiming at the development of biotechnology in the state of Maranhão.