Histone proteins and the nucleosomes they form with DNA are the fundamental building blocks of eukaryotic chromatin. A diverse array of post-translational modifications that often occur on tail domains of these proteins has been well documented. Although the function of these highly conserved modifications has remained elusive, converging biochemical and genetic evidence suggests functions in several chromatin-based processes. We propose that distinct histone modifications, on one or more tails, act sequentially or in combination to form a ‘histone code’ that is, read by other proteins to bring about distinct downstream events.
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Research surrounding this topic in our laboratory is supported by grants from the NIH to C.D.A. and B.D.S. We wish to thank current laboratory members, especially C. A. Mizzen, for critical review of this manuscript, and T. K. Archer and C. L. Smith for kindly sharing unpublished data.
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