Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Methylome profiling of healthy and central precocious puberty girls

Texto completo
Autor(es):
Mostrar menos -
Bessa, Danielle S. [1] ; Maschietto, Mariana [2] ; Aylwin, Carlos Francisco [3] ; Canton, Ana P. M. [4, 1] ; Brito, Vinicius N. [1] ; Macedo, Delanie B. [1] ; Cunha-Silva, Marina [1] ; Palhares, Heloisa M. C. [5] ; de Resende, Elisabete A. M. R. [5] ; Borges, Maria de Fatima [5] ; Mendonca, Berenice B. [1] ; Netchine, Irene [4] ; Krepischi, Ana C. V. [6] ; Lomniczi, Alejandro [3, 7] ; Ojeda, Sergio R. [7] ; Latronico, Ana Claudia [1, 8]
Número total de Autores: 16
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Sao Paulo Med Sch, Clin Hosp, Lab Hormones & Mol Genet, Div Endocrinol & Metab, Dev Endocrinol Unit, LIM42, Sao Paulo, SP - Brazil
[2] Brazilian Ctr Res Energy & Mat CNPEM, Brazilian Biosci Natl Lab LNBio, Campinas, SP - Brazil
[3] OHSU, Oregon Natl Primate Res Ctr, Div Genet, Beaverton, OR - USA
[4] Sorbonne Univ, Hop Armand Trousseau, AP HP, Ctr Rech St Antoine, UMR S 938, INSERM, Explorat Fonct Endocriniennes, Paris - France
[5] Triangulo Mineiro Fed Univ, Div Endocrinol, Uberaba, MG - Brazil
[6] Univ Sao Paulo, Inst Biosci, Dept Genet & Evolutionary Biol, Sao Paulo, SP - Brazil
[7] OHSU, Div Neurosci, Oregon Natl Primate Res Ctr, Beaverton, OR - USA
[8] Univ Sao Paulo, Hosp Clin, Fac Med, Dept Clin Med, Disciplina Endocrinol & Metab, Av Dr Eneas de Carvalho Aguiar 255, 7 Andar, BR-05403900 Sao Paulo - Brazil
Número total de Afiliações: 8
Tipo de documento: Artigo Científico
Fonte: CLINICAL EPIGENETICS; v. 10, NOV 22 2018.
Citações Web of Science: 2
Resumo

BackgroundRecent studies demonstrated that changes in DNA methylation (DNAm) and inactivation of two imprinted genes (MKRN3 and DLK1) alter the onset of female puberty. We aimed to investigate the association of DNAm profiling with the timing of human puberty analyzing the genome-wide DNAm patterns of peripheral blood leukocytes from ten female patients with central precocious puberty (CPP) and 33 healthy girls (15 pre- and 18 post-pubertal). For this purpose, we performed comparisons between the groups: pre- versus post-pubertal, CPP versus pre-pubertal, and CPP versus post-pubertal.ResultsAnalyzing the methylome changes associated with normal puberty, we identified 120 differentially methylated regions (DMRs) when comparing pre- and post-pubertal healthy girls. Most of these DMRs were hypermethylated in the pubertal group (99%) and located on the X chromosome (74%). Only one genomic region, containing the promoter of ZFP57, was hypomethylated in the pubertal group. ZFP57 is a transcriptional repressor required for both methylation and imprinting of multiple genomic loci. ZFP57 expression in the hypothalamus of female rhesus monkeys increased during peripubertal development, suggesting enhanced repression of downstream ZFP57 target genes. Fourteen other zinc finger (ZNF) genes were related to the hypermethylated DMRs at normal puberty. Analyzing the methylome changes associated with CPP, we demonstrated that the patients with CPP exhibited more hypermethylated CpG sites compared to both pre-pubertal (81%) and pubertal (89%) controls. Forty-eight ZNF genes were identified as having hypermethylated CpG sites in CPP.ConclusionMethylome profiling of girls at normal and precocious puberty revealed a widespread pattern of DNA hypermethylation, indicating that the pubertal process in humans is associated with specific changes in epigenetically driven regulatory control. Moreover, changes in methylation of several ZNF genes appear to be a distinct epigenetic modification underlying the initiation of human puberty. (AU)

Processo FAPESP: 13/03236-5 - Novas abordagens e metodologias na investigação genético-molecular dos distúrbios de crescimento e desenvolvimento puberal
Beneficiário:Alexander Augusto de Lima Jorge
Linha de fomento: Auxílio à Pesquisa - Temático
Processo FAPESP: 15/06281-7 - Investigação da regulação epigenética em tumores sólidos pediátricos
Beneficiário:Mariana Camargo Maschietto
Linha de fomento: Bolsas no Brasil - Apoio a Jovens Pesquisadores