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Imprinted gene alterations in the kidneys of growth restricted offspring may be mediated by a long non-coding RNA.
Doan, Thu N A; Cowley, James M; Phillips, Aaron L; Briffa, Jessica F; Leemaqz, Shalem Y; Burton, Rachel A; Romano, Tania; Wlodek, Mary E; Bianco-Miotto, Tina.
Affiliation
  • Doan TNA; School of Agriculture, Food and Wine, & Waite Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Cowley JM; Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Phillips AL; School of Agriculture, Food and Wine, & Waite Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Briffa JF; School of Agriculture, Food and Wine, & Waite Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Leemaqz SY; Department of Anatomy and Physiology, The University of Melbourne, Parkville, Victoria, Australia.
  • Burton RA; Robinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
  • Romano T; SAHMRI Women and Kids, South Australian Health & Medical Research Institute, Adelaide, South Australia, Australia.
  • Wlodek ME; College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
  • Bianco-Miotto T; School of Agriculture, Food and Wine, & Waite Research Institute, University of Adelaide, Adelaide, South Australia, Australia.
Epigenetics ; 19(1): 2294516, 2024 Dec.
Article in En | MEDLINE | ID: mdl-38126131
ABSTRACT
Altered epigenetic mechanisms have been previously reported in growth restricted offspring whose mothers experienced environmental insults during pregnancy in both human and rodent studies. We previously reported changes in the expression of the DNA methyltransferase Dnmt3a and the imprinted genes Cdkn1c (Cyclin-dependent kinase inhibitor 1C) and Kcnq1 (Potassium voltage-gated channel subfamily Q member 1) in the kidney tissue of growth restricted rats whose mothers had uteroplacental insufficiency induced on day 18 of gestation, at both embryonic day 20 (E20) and postnatal day 1 (PN1). To determine the mechanisms responsible for changes in the expression of these imprinted genes, we investigated DNA methylation of KvDMR1, an imprinting control region (ICR) that includes the promoter of the antisense long non-coding RNA Kcnq1ot1 (Kcnq1 opposite strand/antisense transcript 1). Kcnq1ot1 expression decreased by 51% in growth restricted offspring compared to sham at PN1. Interestingly, there was a negative correlation between Kcnq1ot1 and Kcnq1 in the E20 growth restricted group (Spearman's ρ = 0.014). No correlation was observed between Kcnq1ot1 and Cdkn1c expression in either group at any time point. Additionally, there was a 11.25% decrease in the methylation level at one CpG site within KvDMR1 ICR. This study, together with others in the literature, supports that long non-coding RNAs may mediate changes seen in tissues of growth restricted offspring.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / RNA, Long Noncoding Limits: Animals / Female / Humans / Pregnancy Language: En Journal: Epigenetics Journal subject: GENETICA Year: 2024 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Methylation / RNA, Long Noncoding Limits: Animals / Female / Humans / Pregnancy Language: En Journal: Epigenetics Journal subject: GENETICA Year: 2024 Type: Article Affiliation country: Australia