IMR Press / FBL / Volume 14 / Issue 2 / DOI: 10.2741/3251

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.

Open Access Article
Insights into chromatin remodelers in mesenchymal stem cells and differentiation
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1 Department of Cell and Developmental Biology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel
Academic Editor:Eran Meshorer
Front. Biosci. (Landmark Ed) 2009, 14(2), 398–409;
Published: 1 January 2009
(This article belongs to the Special Issue Stem cell chromatin)

Acquisition of lineage specific fate depends on the well orchestrated performance of master transcription factors and on dynamic changes in chromatin structure that account for epigenetic regulation. Epigenetic mechanisms regulate transcription at the promoter level and involve the recruitment of numerous chromatin modifiers in order to permit tissue-selective gene transcription. The dynamics of chromatin structural changes are achieved by the actions of two classes of enzymes: ATP-dependent chromatin remodelers, and histone modifying enzymes. The enzymes are partners in multi-protein complexes that activate or repress transcription depending on the composition of the protein complex. It is fully appreciated now that mechanisms triggering changes in chromatin structure are an integral in determining the stem cell fate. Elucidating the nature of cross talk between chromatin remodelers and master genes is important for identifying pathways that govern stem cell fate and lineage decision.

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