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Biochem Biophys Res Commun. 2011 Jan 28;404(4):1016-22. doi: 10.1016/j.bbrc.2010.12.101. Epub 2010 Dec 25.

The histone methyltransferase Dot1 is required for DNA damage repair and proper development in Dictyostelium.

Author information

1
Institute for Anatomy and Cell Biology, Schillerstr. 42, Ludwig Maximilians University of Munich, 80336 Munich, Germany. amueller@lrz.uni-muenchen.de

Abstract

Posttranslational histone modifications play an important role in modulating gene expression and chromatin structure. Here we report the identification of histone H3K79 dimethylation in the simple eukaryote Dictyostelium discoideum. We have deleted the D. discoideum Dot1/KMT4 homologue and demonstrate that it is the sole enzyme responsible for histone H3K79me2. Cells lacking Dot1 are reduced in growth and delayed in development, but do not show apparent changes in cell cycle regulation. Furthermore, our results indicate that Dot1 contributes to UV damage resistance and DNA repair in D. discoideum. In summary, the data support the view that the machinery controlling the setting of histone marks is evolutionary highly conserved and provide evidence that D. discoideum is a suitable model system to analyze these modifications and their functions during development and differentiation.

PMID:
21187070
DOI:
10.1016/j.bbrc.2010.12.101
[Indexed for MEDLINE]

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