Literature DB >> 17981649

Developmentally-poised chromatin of embryonic stem cells.

Theodore P Rasmussen1.   

Abstract

Embryonic stem (ES) cells proliferate indefinitely while maintaining pluripotency. The ability of ES cells to form all cell-types of the embryo can occur because they maintain their genome in an epigenetically-potentiated state that is amenable to a broad series of changes in gene expression. Epigenetic stasis and change occur at a molecular level largely through mechanisms involving chromatin and its modification. This review outlines current knowledge of chromatin homeostasis in undifferentiated ES cells, and the remodeling of chromatin during the course of ES cell differentiation. Furthermore, recent evidence shows that the chromatin of many genes in ES cells is configured in developmentally-potentiated states that index them for later transcriptional outcomes. ES cell chromatin also has dynamic physical and kinetic properties that are probably necessary for rapid and pervasive remodeling upon differentiation. Finally, knowledge of nuclear reprogramming activities in oocytes and ES cells are considered, since these activities may also function in the maintenance of pluripotent ES cell chromatin and are also likely involved in subsequent differentiation.

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Year:  2008        PMID: 17981649     DOI: 10.2741/2781

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  5 in total

1.  Dynamics of the transcriptome response of cultured human embryonic stem cells to ionizing radiation exposure.

Authors:  Mykyta V Sokolov; Irina V Panyutin; Igor G Panyutin; Ronald D Neumann
Journal:  Mutat Res       Date:  2011-03-03       Impact factor: 2.433

Review 2.  Epigenetic remodeling of chromatin architecture: exploring tumor differentiation therapies in mesenchymal stem cells and sarcomas.

Authors:  Sara Siddiqi; Joslyn Mills; Igor Matushansky
Journal:  Curr Stem Cell Res Ther       Date:  2010-03       Impact factor: 3.828

3.  Looking into the black box: insights into the mechanisms of somatic cell reprogramming.

Authors:  Laurent David; Payman Samavarchi-Tehrani; Azadeh Golipour; Jeffrey L Wrana
Journal:  Genes (Basel)       Date:  2011-01-13       Impact factor: 4.096

4.  HDAC stimulates gene expression through BRD4 availability in response to IFN and in interferonopathies.

Authors:  Isabelle J Marié; Hao-Ming Chang; David E Levy
Journal:  J Exp Med       Date:  2018-11-21       Impact factor: 14.307

5.  Histone modifications and lamin A regulate chromatin protein dynamics in early embryonic stem cell differentiation.

Authors:  Shai Melcer; Hadas Hezroni; Eyal Rand; Malka Nissim-Rafinia; Arthur Skoultchi; Colin L Stewart; Michael Bustin; Eran Meshorer
Journal:  Nat Commun       Date:  2012-06-19       Impact factor: 14.919

  5 in total

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