The inhibition of checkpoint activation by telomeres does not involve exclusion of dimethylation of histone H4 lysine 20 (H4K20me2) [version 2; peer review: 2 approved, 1 not approved]

• Published in: F1000 research 2018, Vol.7, p.1027
• Main Authors: Audry, Julien, Wang, Jinyu, Eisenstatt, Jessica R, Berkner, Kathleen L, Runge, Kurt W
• Format: Article
• Language: English
• Subjects: Cell cycle; Cell Cycle Checkpoints; Chromatin; Chromosomes; Cloning; Copyright; Datasets; Deoxyribonucleic acid; DNA; DNA Damage; DNA methylation; Enzymes; Genes; Genomes; Histone H4; Histones - genetics; Histones - metabolism; Lysine; Medicine; Methylation; Nucleosomes; Proteins; Research Note; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae - metabolism; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Schizosaccharomyces - genetics; Schizosaccharomyces - metabolism; Schizosaccharomyces pombe Proteins - genetics; Schizosaccharomyces pombe Proteins - metabolism; Signal transduction; Single-stranded DNA; Telomerase; Telomere - genetics; Telomere - metabolism; Telomeres; Yeast
• ISSN: 2046-1402; 2046-1402
• DOI: 10.12688/f1000research.15166.2

DNA double-strand breaks (DSBs) activate the DNA damage checkpoint machinery to pause or halt the cell cycle.  Telomeres, the specific DNA-protein complexes at linear eukaryotic chromosome ends, are capped DSBs that do not activate DNA damage checkpoints.  This "checkpoint privileged" status of telomeres was previously investigated in the yeast  Schizosaccharomyces pombelacking the major double-stranded telomere DNA binding protein Taz1. Telomeric DNA repeats in cells lacking Taz1 are 10 times longer than normal and contain single-stranded DNA regions. DNA damage checkpoint proteins associate with these damaged telomeres, but the DNA damage checkpoint is not activated. This severing of the DNA damage checkpoint signaling pathway was reported to stem from exclusion of histone H4 lysine 20 dimethylation (H4K20me2) from telomeric nucleosomes in both wild type cells and cells lacking Taz1.  However, experiments to identify the mechanism of this exclusion failed, prompting our re-evaluation of H4K20me2 levels at telomeric chromatin.  In this short report, we used an extensive series of controls to identify an antibody specific for the H4K20me2 modification and show that the level of this modification is the same at telomeres and internal loci in both wild type cells and those lacking Taz1.  Consequently, telomeres must block activation of the DNA Damage Response by another mechanism that remains to be determined.