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Science 293 (5532): 1074-1080
Copyright © 2001 by the American Association for the Advancement of Science
Translating the Histone Code
Thomas Jenuwein,1
C. David Allis2
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 Research Institute of Molecular Pathology
(IMP) at the Vienna Biocenter, Dr. Bohrgasse 7, A-1030 Vienna, Austria.
E-mail: jenuwein{at}nt.imp.univie.ac.at
2 Department
of Biochemistry and Molecular Genetics, University of Virginia Health
Science Center, Charlottesville, VA 22908, USA. E-mail:
allis{at}virginia.edu
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- Identification and Characterization of Nardilysin as a Novel Dimethyl H3K4-binding Protein Involved in Transcriptional Regulation.
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- The Viral Protein Tat Can Inhibit the Establishment of HIV-1 Latency.
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- LSD1 cooperates with CTIP2 to promote HIV-1 transcriptional silencing.
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- 212Pb-Radioimmunotherapy Induces G2 Cell-Cycle Arrest and Delays DNA Damage Repair in Tumor Xenografts in a Model for Disseminated Intraperitoneal Disease.
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