A cassette system to study embryonic stem cell differentiation by inducible RNA interference.

Stem Cells

Institute for Medical Microbiology, Department of Biological and Clinical Sciences, University of Basel, Basel, Switzerland.

Published: May 2007

AI Article Synopsis

  • The study explores how post-transcriptional mechanisms impact early differentiation of embryonic stem (ES) cells, which is less understood compared to transcription factors.
  • A new system using small hairpin (sh)RNAs allows targeted gene silencing in ES cells, enabling researchers to study specific gene functions related to differentiation.
  • The research highlights Brf1 as a significant regulator in cardiomyocyte formation, suggesting that post-transcriptional regulation plays a crucial role in early development and has potential implications for regenerative medicine.

Article Abstract

Although differentiation of pluripotent embryonic stem cells is restricted by a hierarchy of transcription factors, little is known about whether post-transcriptional mechanisms similarly regulate early embryoid differentiation. We developed a system where small hairpin (sh)RNAs can be induced in embryonic stem (ES) cells from a defined locus following integration by Flp recombinase-mediated DNA recombination. To verify the system, the key transcription factor Stat3, which maintains pluripotency, was downregulated by shRNA, and the expected morphological and biochemical markers of differentiation were observed. Induction of shRNA specific for the post-transcriptional regulator Brf1 (Zfp36L1) amplified the cardiac markers with strong stimulation of cardiomyocyte formation within embryoid bodies. These findings identify Brf1 as a novel potential regulator of cardiomyocyte formation and suggest that post-transcriptional mechanisms are of importance to early development and, possibly, to regenerative medicine. The inducible RNA interference system presented here should also allow assignment of function for candidate genes with suspected roles in ES cell development. Disclosure of potential conflicts of interest is found at the end of this article.

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Source
http://dx.doi.org/10.1634/stemcells.2006-0106DOI Listing

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