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Chromatin, the physiological template of all eukaryotic genetic information, is subject to a diverse array of posttranslational modifications that largely impinge on histone amino termini, thereby regulating access to the underlying DNA. Distinct histone amino-terminal modifications can generate synergistic or antagonistic interaction affinities for chromatin-associated proteins, which in turn dictate dynamic transitions between transcriptionally active or transcriptionally silent chromatin states. The combinatorial nature of histone amino-terminal modifications thus reveals a "histone code" that considerably extends the information potential of the genetic code. We propose that this epigenetic marking system represents a fundamental regulatory mechanism that has an impact on most, if not all, chromatin-templated processes, with far-reaching consequences for cell fate decisions and both normal and pathological development.
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Thomas Jenuwein
University of Vienna
C. David Allis
The Wistar Institute
Science
University of Virginia
Research Institute of Molecular Pathology
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Jenuwein et al. (Fri,) studied this question.
synapsesocial.com/papers/69d7d7dd05ee2ba81dbee4d4 — DOI: https://doi.org/10.1126/science.1063127