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Epigenetic Mechanisms in Hirschsprung Disease. | LitMetric

Epigenetic Mechanisms in Hirschsprung Disease.

Int J Mol Sci

Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.

Published: June 2019

AI Article Synopsis

  • Hirschsprung disease (HSCR) occurs when enteric precursor cells fail to properly develop during the formation of the Enteric Nervous System (ENS), leading to issues in bowel function.
  • The regulation of gene expression through various mechanisms, including epigenetics and transcriptional controls, is crucial for the proper development and functioning of ENS.
  • This review focuses on how epigenetic factors at both transcriptional and posttranscriptional levels influence neural crest cells and contribute to conditions like HSCR.

Article Abstract

Hirschsprung disease (HSCR, OMIM 142623) is due to a failure of enteric precursor cells derived from neural crest (EPCs) to proliferate, migrate, survive or differentiate during Enteric Nervous System (ENS) formation. This is a complex process which requires a strict regulation that results in an ENS specific gene expression pattern. Alterations at this level lead to the onset of neurocristopathies such as HSCR. Gene expression is regulated by different mechanisms, such as DNA modifications (at the epigenetic level), transcriptional mechanisms (transcription factors, silencers, enhancers and repressors), postranscriptional mechanisms (3'UTR and ncRNA) and regulation of translation. All these mechanisms are finally implicated in cell signaling to determine the migration, proliferation, differentiation and survival processes for correct ENS development. In this review, we have performed an overview on the role of epigenetic mechanisms at transcriptional and posttranscriptional levels on these cellular events in neural crest cells (NCCs), ENS development, as well as in HSCR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6650840PMC
http://dx.doi.org/10.3390/ijms20133123DOI Listing

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