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Epigenetic Regulation and Transcriptional Memory in Development; Selection Facilitating Prudence Publisher Pubmed



Verma A1 ; Maini J1 ; Jain S1, 2 ; Ghasemi M1, 3 ; Kohli S1 ; Brahmachari V1
Authors
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Authors Affiliations
  1. 1. Dr. B.R. Ambedkar Center for Biomedical Research, University of Delhi, Delhi, India
  2. 2. Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, 160 91, Sweden
  3. 3. Department of Genetics, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, 146, South Gandhi Ave, Vanak Sq, Tehran, Iran

Source: International Journal of Developmental Biology Published:2020


Abstract

The epigenetic mechanisms regulating developmental gene expression are examples of a strategy to generate unique expression profiles with global regulators controlling several genes. In a simplified view, a common set of tools, that include DNA motif recognizing proteins (recruiters), binding/interacting surfaces (ARPs-actin related proteins), epigenetic writers (histone methyltransferases, acetylases), readers (chromatin remodeling proteins, PRC1 members) and erasers (demethylases, deacetylases) form complexes which not only regulate transcription, but also retain the transcriptional memory through mitosis. There are two arms of epigenetic regulation: covalent modification of DNA and the post-translational modification of histones. In this review, we discuss both of these aspects briefly to illustrate functional diversity. We discuss our efforts at utilization of the genome sequence data for de novo identification of new players and their functional validation in this remarkable process. © 2020 UPV/EHU Press.