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Trapoxin is a microbially derived cyclotetrapeptide that inhibits histone deacetylation in vivo and causes mammalian cells to arrest in the cell cycle. A trapoxin affinity matrix was used to isolate two nuclear proteins that copurified with histone deacetylase activity. Both proteins were identified by peptide microsequencing, and a complementary DNA encoding the histone deacetylase catalytic subunit (HD1) was cloned from a human Jurkat T cell library. As the predicted protein is very similar to the yeast transcriptional regulator Rpd3p, these results support a role for histone deacetylase as a key regulator of eukaryotic transcription.
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Jack Taunton
University of British Columbia
Christian A. Hassig
Boundless Bio (United States)
Stuart L. Schreiber
Broad Institute
Science
Howard Hughes Medical Institute
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Taunton et al. (Fri,) studied this question.
synapsesocial.com/papers/6a0730352edded7c7b842c88 — DOI: https://doi.org/10.1126/science.272.5260.408