Cell Cycle– and Chaperone-Mediated Regulation of H3K56ac Incorporation in Yeast
2008

Cell Cycle Regulation of Histone H3K56 Acetylation in Yeast

publication 10 minutes Evidence: high

Author Information

Author(s): Tommy Kaplan, Chih Long Liu, Judith A. Erkmann, John Holik, Michael Grunstein, Paul D. Kaufman, Nir Friedman, Oliver J. Rando

Primary Institution: The Hebrew University, Jerusalem, Israel

Hypothesis

How does H3K56 acetylation influence histone incorporation during the cell cycle?

Conclusion

H3K56 acetylation marks nucleosomes incorporated during both replication-coupled and replication-independent processes, and enhances histone turnover.

Supporting Evidence

  • H3K56ac is found at all known sites of nucleosome incorporation.
  • Replication-independent histone turnover is correlated with H3K56ac levels.
  • H3K56ac enhances histone replacement rates at specific genomic loci.

Takeaway

This study shows that a special mark on histones helps them get added to DNA during the cell cycle, making it easier for new histones to replace old ones.

Methodology

The study used single-nucleosome resolution mapping to analyze H3K56 acetylation levels in yeast during different cell cycle phases.

Limitations

The study primarily focuses on yeast, which may limit the generalizability of the findings to other organisms.

Digital Object Identifier (DOI)

10.1371/journal.pgen.1000270

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