Autor(es):
Mendes, Cristiani Cortez ; Zampieri, Bruna Lancia ; Arantes, Lidia Maria Rebolho Batista ; Melendez, Matias Eliseo ; Biselli, Joice Matos [UNESP] ; Carvalho, André Lopes ; Eberlin, Marcos Nogueira ; Riccio, Maria Francesca ; Vannucchi, Hélio ; Carvalho, Valdemir Melechco ; Goloni-Bertollo, Eny Maria ; Pavarino, Érika Cristina
Data: 2022
Identificador Persistente: http://hdl.handle.net/11449/229362
Origem: Oasisbr
Assunto(s): Alu elements; DNA methylation; Down syndrome; Long interspersed nucleotide elements; Polymorphism, Genetic
Descrição
Made available in DSpace on 2022-04-29T08:32:07Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-11-01
Down syndrome (DS) is the most common chromosomal disorder, resulting from the failure of normal chromosome 21 segregation. Studies have suggested that impairments within the one-carbon metabolic pathway can be of relevance for the global genome instability observed in mothers of individuals with DS. Based on the association between global DNA hypomethylation, genome instability, and impairments within the one-carbon metabolic pathway, the present study aimed to identify possible predictors, within the one-carbon metabolism, of global DNA methylation, measured by methylation patterns of LINE-1 and Alu repetitive sequences, in mothers of individuals with DS and mothers of individuals without the syndrome. In addition, we investigated one-carbon genetic polymorphisms and metabolites as maternal predisposing factors for the occurrence of trisomy 21 in children. Eighty-three samples of mothers of children with DS with karyotypically confirmed free trisomy 21 (case group) and 84 of mothers who had at least one child without DS or any other aneuploidy were included in the study. Pyrosequencing assays were performed to access global methylation. The results showed that group affiliation (case or control), betaine-homocysteine methyltransferase (BHMT) G742A and transcobalamin 2 (TCN2) C776G polymorphisms, and folate concentration were identified as predictors of global Alu DNA methylation values. In addition, thymidylate synthase (TYMS) 28-bp repeats 2R/3R or 3R/3R genotypes are independent maternal predisposing factors for having a child with DS. This study adds evidence that supports the association of impairments in the one-carbon metabolism, global DNA methylation, and the possibility of having a child with DS.
Unidade de Pesquisa em Genética e Biologia Molecular-UPGEM Departamento de Biologia Molecular Faculdade de Medicina de São José do Rio Preto-FAMERP
Hospital Israelita Albert Einstein
Molecular Oncology Research Center Barretos Cancer Hospital
Universidade Estadual Paulista Júlio de Mesquita Filho Instituto de Biociências Letras e Ciências Exatas de São José do Rio Preto Departamento de Ciências Biológicas
Universidade Presbiteriana Mackenzie Discovery-Mackenzie-Núcleo Mackenzie de Pesquisa Núcleo Mackenzie de Pesquisas em Ciência Fé e Sociedade
Instituto de Pesquisa Dr. Domingos A. Boldrini
Laboratório de Nutrição Departamento de Clínica Médica Faculdade de Medicina de Ribeirão Preto-USP
Fleury-Centro de Medicina Diagnóstica
Universidade Estadual Paulista Júlio de Mesquita Filho Instituto de Biociências Letras e Ciências Exatas de São José do Rio Preto Departamento de Ciências Biológicas
