This article discusses the advances made in epigenetic research using the model organism fission yeast Schizosaccharomyces pombe. S. pombe has been used for epigenetic research since the discovery of position effect variegation (PEV). This is a phenomenon in which a transgene inserted within heterochromatin is variably expressed, but can be stably inherited in subsequent cell generations. PEV occurs at centromeres, telomeres, ribosomal DNA (rDNA) loci, and mating-type regions of S. pombe chromosomes. Heterochromatin assembly in these regions requires enzymes that modify histones and the RNA interference (RNAi) machinery. One of the key histone-modifying enzymes is the lysine methyltransferase Clr4, which methylates histone H3 on lysine 9 (H3K9), a classic hallmark of heterochromatin. The kinetochore is assembled on specialized chromatin in which histone H3 is replaced by the variant CENP-A. Studies in fission yeast have contributed to our understanding of the establishment and maintenance of CENP-A chromatin and the epigenetic activation and inactivation of centromeres. Outline 1 Schizosaccharomyces pombe life cycle 2 Screens to identify heterochromatin components 3 Different types of heterochromatin 4 S. pombe centromeres: A paradigm for studying heterochromatin 5 S. pombe central domain chromatin and kinetochores 6 Heterochromatin formation at other silent regions 7 Nucleosome remodeling in S. pombe 8 Nuclear organization in S. pombe
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Allshire et al. (2015) studied this question.
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