Your browser doesn't support javascript.
loading
Impact of prematurity on LINE-1 promoter methylation.
Dos Santos, Paulo Victor Barbosa Eleutério; Brasil, Aline de Araújo; Milone, Leo Travassos Vieira; Chalfun, Georgia; Saide, Stephanie Cristina Alves de Oliveira; Salú, Margarida Dos Santos; de Oliveira, Mariana Barros Genuíno; Robaina, Jaqueline Rodrigues; Lima-Setta, Fernanda; Rodrigues-Santos, Gustavo; de Magalhães-Barbosa, Maria Clara; da Cunha, Antônio José Ledo Alves; Prata-Barbosa, Arnaldo.
Affiliation
  • Dos Santos PVBE; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • Brasil AA; Martagão Gesteira Institute of Childcare & Pediatrics (IPPMG), Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
  • Milone LTV; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • Chalfun G; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • Saide SCAO; Institute of Genetics, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
  • Salú MDS; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • de Oliveira MBG; Department of Neonatology, Maternity School, Federal University of Rio de Janeiro (UFRJ), RJ, Brazil.
  • Robaina JR; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • Lima-Setta F; Institute of Genetics, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
  • Rodrigues-Santos G; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • de Magalhães-Barbosa MC; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • da Cunha AJLA; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
  • Prata-Barbosa A; Department of Pediatrics, D'Or Institute for Research & Education (IDOR), Rio de Janeiro, RJ, Brazil.
Epigenomics ; 16(18): 1253-1264, 2024.
Article in En | MEDLINE | ID: mdl-39297700
ABSTRACT

Aim:

Promoter methylation of LINE-1 may be affected by prematurity, but there is little evidence in the literature.Materials &

methods:

Blood from premature and full-term neonates on days 0, 5, 30 and 90 was analyzed for DNA methylation percentage in a promoter region of the LINE-1, after bisulfite conversion and pyrosequencing.

Results:

Premature infants, as a whole, showed significantly lower methylation percentage at birth, but this difference diminished over time. However, the subgroup of extremely premature (<28 weeks gestational age) had higher methylation percentages, similar to full-term newborns.

Conclusion:

This research underscores the critical role of prematurity on the methylation pattern of LINE-1. These findings underline the complexity of epigenetic regulation in prematurity and emphasize the need for further studies.
Premature birth can have significant effects on a baby's development and long-term health. This study investigates how being born prematurely affects a process called DNA methylation, which can influence how genes are turned on or off. Specifically, we examined the LINE-1 promoter, a frequently occurring region of DNA known for its role in regulating gene activity.We collected blood samples from both premature and full-term newborns at birth and at several points in the early months of life. Our findings showed that premature babies have lower levels of LINE-1 promoter methylation at birth compared with full-term babies. These differences in methylation could possibly affect the babies' development and health as they grow.Our research highlights the need for continued study in this area to explore how these epigenetic changes impact long-term health and to develop strategies to mitigate these effects.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Infant, Premature / Promoter Regions, Genetic / DNA Methylation / Long Interspersed Nucleotide Elements Limits: Female / Humans / Male / Newborn Language: En Journal: Epigenomics Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Infant, Premature / Promoter Regions, Genetic / DNA Methylation / Long Interspersed Nucleotide Elements Limits: Female / Humans / Male / Newborn Language: En Journal: Epigenomics Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United kingdom