| Literature DB >> 22555599 |
Cheng-Ran Xu1, Kenneth S Zaret.
Abstract
Understanding the basis for multipotency, whereby stem cells and other progenitors can differentiate into certain tissues and not others, provides insights into the mechanism of cell programming in development, homeostasis, and disease. We recently reported a screen of diverse chromatin marks to obtain clues about chromatin states in the multipotent embryonic endoderm. Genetic and pharmacologic tests of certain marks' function demonstrated that the relevant chromatin modifying factors modulate the fate choice for liver or pancreas induction in the endoderm. The information about chromatin states from embryonic studies can be used to predict lineage-specific developmental potential and chromatin modifiers to enhance particular cell fate transitions from stem cells.Mesh:
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Year: 2012 PMID: 22555599 PMCID: PMC3383570 DOI: 10.4161/nucl.19321
Source DB: PubMed Journal: Nucleus ISSN: 1949-1034 Impact factor: 4.197