Literature DB >> 33336687

Keeping your options open: insights from Dppa2/4 into how epigenetic priming factors promote cell plasticity.

Mélanie A Eckersley-Maslin1,2,3.   

Abstract

The concept of cellular plasticity is particularly apt in early embryonic development, where there is a tug-of-war between the stability and flexibility of cell identity. This balance is controlled in part through epigenetic mechanisms. Epigenetic plasticity dictates how malleable cells are to change by adjusting the potential to initiate new transcriptional programmes. The higher the plasticity of a cell, the more readily it can adapt and change its identity in response to external stimuli such as differentiation cues. Epigenetic plasticity is regulated in part through the action of epigenetic priming factors which establish this permissive epigenetic landscape at genomic regulatory elements to enable future transcriptional changes. Recent studies on the DNA binding proteins Developmental Pluripotency Associated 2 and 4 (Dppa2/4) support their roles as epigenetic priming factors in facilitating cell fate transitions. Here, using Dppa2/4 as a case study, the concept of epigenetic plasticity and molecular mechanism of epigenetic priming factors will be explored. Understanding how epigenetic priming factors function is key not only to improve our understanding of the tight control of development, but also to give insights into how this goes awry in diseases of cell identity, such as cancer.
© 2020 The Author(s).

Entities:  

Keywords:  Dppa2/4; cell fate; chromatin; epigenetic priming; epigenetics; plasticity

Mesh:

Substances:

Year:  2020        PMID: 33336687      PMCID: PMC7752079          DOI: 10.1042/BST20200873

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  3 in total

Review 1.  Regulation, functions and transmission of bivalent chromatin during mammalian development.

Authors:  Trisha A Macrae; Julie Fothergill-Robinson; Miguel Ramalho-Santos
Journal:  Nat Rev Mol Cell Biol       Date:  2022-08-26       Impact factor: 113.915

2.  DPPA2 and DPPA4 are dispensable for mouse zygotic genome activation and pre-implantation development.

Authors:  Zhiyuan Chen; Zhenfei Xie; Yi Zhang
Journal:  Development       Date:  2021-12-21       Impact factor: 6.868

3.  Maternal Dppa2 and Dppa4 are dispensable for zygotic genome activation but important for offspring survival.

Authors:  Oana Kubinyecz; Fatima Santos; Deborah Drage; Wolf Reik; Melanie A Eckersley-Maslin
Journal:  Development       Date:  2021-12-21       Impact factor: 6.868

  3 in total

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