Stage-Specific Transcription Factors Drive Astrogliogenesis by Remodeling Gene Regulatory Landscapes.

Cell Stem Cell

Institute of Physiological Chemistry, University Medical Center Johannes Gutenberg University Mainz, 55128 Mainz, Germany; Focus Program Translational Neuroscience, Johannes Gutenberg University Mainz, 55131 Mainz, Germany; Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE1 1UL, UK; MRC Centre for Neurodevelopmental Disorders, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE1 1UL, UK. Electronic address:

Published: October 2018

AI Article Synopsis

  • A research study investigates how neural stem cells develop into astrocytes during brain development using a combination of transcriptomic and epigenomic analyses.
  • The researchers discovered distinct phases of astrogliogenesis with unique gene expression profiles and chromatin states, highlighting the importance of specific regulatory elements.
  • Key transcription factors NFIA and ATF3 were found to drive the differentiation process, while RUNX2 promotes the maturation of astrocytes by activating gene expression programs.

Article Abstract

A broad molecular framework of how neural stem cells are specified toward astrocyte fate during brain development has proven elusive. Here we perform comprehensive and integrated transcriptomic and epigenomic analyses to delineate gene regulatory programs that drive the developmental trajectory from mouse embryonic stem cells to astrocytes. We report molecularly distinct phases of astrogliogenesis that exhibit stage- and lineage-specific transcriptomic and epigenetic signatures with unique primed and active chromatin regions, thereby revealing regulatory elements and transcriptional programs underlying astrocyte generation and maturation. By searching for transcription factors that function at these elements, we identified NFIA and ATF3 as drivers of astrocyte differentiation from neural precursor cells while RUNX2 promotes astrocyte maturation. These transcription factors facilitate stage-specific gene expression programs by switching the chromatin state of their target regulatory elements from primed to active. Altogether, these findings provide integrated insights into the genetic and epigenetic mechanisms steering the trajectory of astrogliogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179960PMC
http://dx.doi.org/10.1016/j.stem.2018.09.008DOI Listing

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