Translating the Histone Code

Перевод «гистонового кода»
C. David Allis, Thomas Jenuwein
2001-08-10

chromatin-associated proteinsepigenetic markinghistone amino-terminal modificationshistone codeposttranslational modifications
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.
1
Combinations of distinct histone amino-terminal modifications generate synergistic or antagonistic interaction affinities, forming a combinatorial 'histone code'.
2
Histone amino-terminal posttranslational modifications regulate DNA accessibility by affecting chromatin-associated protein interactions.
3
Histone-based epigenetic regulation has broad consequences for normal development and pathological conditions.
4
The histone code expands information potential beyond the genetic code, directing dynamic transitions between transcriptionally active and silent chromatin states.
5
This epigenetic marking system is proposed as a fundamental regulatory mechanism influencing most chromatin-templated processes and cell fate decisions.

Histone amino-terminal posttranslational modifications on chromatin (the histone code)

How combinations of histone N-terminal modifications encode regulatory information by modulating interaction affinities for chromatin-associated proteins to control transitions between transcriptionally active and silent chromatin states and thereby influence chromatin-templated processes and cell fate

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2001-08-10
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C. David Allis
Thomas Jenuwein
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