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(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.)

ilencing mark H3K27me3 is differently reprogrammed in bovine embryos with distinct kinetics of developmen

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Autor(es):
Ispada, Jessica [1, 2] ; Milazzotto, Marcella Pecora [1, 2]
Número total de Autores: 2
Afiliação do(s) autor(es):
[1] Fed Univ ABC, Ctr Nat & Human Sci, Lab Cellular & Mol Biol, Santo Andre, SP - Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Butanta - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: REPRODUCTION IN DOMESTIC ANIMALS; v. 57, n. 3 DEC 2021.
Citações Web of Science: 0
Resumo

The kinetics of the first cleavages is a predictor of blastocyst development and implantation. For bovine embryos, this attribute was previously related to distinct metabolic, molecular and epigenetic profiles, including DNA and histone modifications. In the present work, we described the dynamics of trimethylation of lysine 27 on histone H3 (H3K27me3) in fast and slow developing embryos and verified if this epigenetic mark was also influenced by the speed of the first cleavages. In vitro-produced bovine embryos were classified as fast (4 or more cells) or slow (2 cells) at 40 hr post fertilization (hpf) and either collected or cultured until 96 hpf or 186 hpf. Immunofluorescence analysis was performed in these three time points and showed that although both groups presented the same levels of H3K27me3 at 40 hpf, slow embryos presented a pronounced increase in this mark at 186 hpf when compared to fast embryos, resulting in blastocysts with remarkable differences in H3K27me3 levels. In conclusion, the increased levels of this repressive histone post-translation modification (PTM) might be an attempt of slow embryos to promote gene expression control and chromatin integrity, since it was already reported that these embryos present reduced levels of other epigenetic repressive marks as DNA methylation and trimethylation of lysine 9 on histone H3 (H3K9me3). (AU)

Processo FAPESP: 18/11668-6 - Metaboloepigenética: Interrelação entre o metabolismo energético e a metilação do DNA em embriões bovinos
Beneficiário:Jéssica Ispada
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 15/03381-0 - Estresse celular e sua relação com a cinética de desenvolvimento de embriões bovinos produzidos in vitro
Beneficiário:Marcella Pecora Milazzotto
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 19/25982-7 - Regulação metabólica da metilação do DNA: novas rotas, novos alvos
Beneficiário:Marcella Pecora Milazzotto
Modalidade de apoio: Auxílio à Pesquisa - Regular