5-hydroxymethyl-cytosine enrichment of non-committed cells is not a universal feature of vertebrate development

  • Rimple D. Almeida
  • , Matthew Loose
  • , Virginie Sottile
  • , Elena Matsa
  • , Chris Denning
  • , Lorraine Young
  • , Andrew D. Johnson
  • , Martin Gering
  • , Alexey Ruzov

Research output: Contribution to journalArticlepeer-review

Abstract

5-hydroxymethyl-cytosine (5-hmC) is a cytosine modification that is relatively abundant in mammalian pre-implantation embryos and embryonic stem cells (ESC) derived from mammalian blastocysts. Recent observations imply that both 5-hmC and Tet1/2/3 proteins, catalyzing the conversion of 5-methyl-cytosine to 5-hmC, may play an important role in self renewal and differentiation of ESCs. Here we assessed the distribution of 5-hmC in zebrafish and chick embryos and found that, unlike in mammals, 5-hmC is immunochemically undetectable in these systems before the onset of organogenesis. In addition, Tet1/2/3 transcripts are either low or undetectable at corresponding stages of zebrafish development. However, 5-hmC is enriched in later zebrafish and chick embryos and exhibits tissue-specific distribution in adult zebrafish. Our findings show that 5-hmC enrichment of non-committed cells is not a universal feature of vertebrate development and give insights both into evolution of embryonic pluripotency and the potential role of 5-hmC in its regulation.

Original languageEnglish
Pages (from-to)383-389
Number of pages7
JournalEpigenetics
Volume7
Issue number4
DOIs
Publication statusPublished - Apr 2012
Externally publishedYes

Keywords

  • 5-hydroxymethyl-cytosine
  • 5-methyl-cytosine
  • CpG methylation
  • Development
  • Embryonic stem cells
  • Epigenetics
  • Evolution
  • Pluripotency
  • References
  • Tet1/2/3 proteins

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