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Epigenetic restriction of embryonic cell lineage fate by methylation of Elf5. | LitMetric

Epigenetic restriction of embryonic cell lineage fate by methylation of Elf5.

Nat Cell Biol

Laboratory of Developmental Genetics and Imprinting, The Babraham Institute, Cambridge CB22 3AT, UK.

Published: November 2008

AI Article Synopsis

  • Mouse embryonic stem (ES) cells can develop into all three germ layers but usually do not form trophoblast cells, which are crucial for placental development.
  • Researchers discovered that ES cells lacking DNA methylation can more effectively differentiate into trophoblast cells, identifying the transcription factor Elf5 as a key regulator.
  • Elf5 helps promote the expression of other trophoblast cell factors and serves as a "gatekeeper," influencing whether cells commit to trophoblast identity or revert to a more flexible state in early development, linking to developmental canalization theory.

Article Abstract

Mouse ES cells can differentiate into all three germ layers of the embryo but are generally excluded from the trophoblast lineage. Here we show that ES cells deficient in DNA methylation can differentiate efficiently into trophoblast derivatives. In a genome-wide screen we identified the transcription factor Elf5 as methylated and repressed in ES cells, and hypomethylated and expressed in TS and methylation-deficient ES cells. Elf5 creates a positive-feedback loop with the TS cell determinants Cdx2 and Eomes that is restricted to the trophoblast lineage by epigenetic regulation of Elf5. Importantly, the late-acting function of Elf5 allows initial plasticity and regulation in the early blastocyst. Thus, Elf5 functions as a gatekeeper, downstream of initial lineage determination, to reinforce commitment to the trophoblast lineage or to abort this pathway in epiblast cells. This epigenetic restriction of cell lineage fate provides a molecular mechanism for Waddington's concept of canalization of developmental pathways.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635539PMC
http://dx.doi.org/10.1038/ncb1786DOI Listing

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