Messenger RNA and microRNA profiling during early mouse EB formation

Rashmi Tripathi, Harpreet Kaur Saini, Roland Rad, Cei Abreu-Goodger, Stijn Van Dongen, Anton J. Enright

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Embryonic stem (ES) cells can be induced to differentiate into embryoid bodies (EBs) in a synchronised manner when plated at a fixed density in hanging drops. This differentiation procedure mimics post-implantation development in mouse embryos and also serves as the starting point of protocols used in differentiation of stem cells into various lineages. Currently, little is known about the potential influence of microRNAs (miRNAs) on mRNA expression patterns during EB formation. We have measured mRNA and miRNA expression in developing EBs plated in hanging drops until day 3, when discrete structural changes occur involving their differentiation into three germ layers. We observe significant alterations in mRNA and miRNA expression profiles during this early developmental time frame, in particular of genes involved in germ layer formation, stem cell pluripotency and nervous system development. Computational target prediction using Pictar, TargetScan and miRBase Targets reveals an enrichment of binding sites corresponding to differentially and highly expressed miRNAs in stem cell pluripotency genes and a neuroectodermal marker, Nes. We also find that members of let-7 family are significantly down-regulated at day 3 and the corresponding up-regulated genes are enriched in let-7 seed sequences. These results depict how miRNA expression changes may affect the expression of mRNAs involved in EB formation on a genome-wide scale. Understanding the regulatory effects of miRNAs during EB formation may enable more efficient derivation of different cell types in culture.

Original languageEnglish
Pages (from-to)334-344
Number of pages11
JournalGene Expression Patterns
Volume11
Issue number5-6
DOIs
StatePublished - Jun 2011
Externally publishedYes

Keywords

  • EBs
  • Embryonic stem cells
  • Gene ontology
  • Germ layer
  • Let-7
  • Lin28
  • Messenger RNA
  • MicroRNA
  • MicroRNA targets
  • Nervous system development
  • Pluripotency

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