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Epigenetic Regulation of Chromatin States inSchizosaccharomyces pombe
Author(s) -
Robin C. Allshire,
Karl Ekwall
Publication year - 2015
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a018770
Subject(s) - biology , schizosaccharomyces pombe , heterochromatin , epigenetics , centromere , chromatin , histone code , heterochromatin protein 1 , genetics , histone methyltransferase , schizosaccharomyces , histone methylation , histone , histone h2a , microbiology and biotechnology , nucleosome , dna methylation , dna , chromosome , saccharomyces cerevisiae , yeast , gene , gene expression
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.

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