• Open Access

RNA and epigenetic silencing: Insight from fission yeast

Authors

  • Derek B. Goto,

    Corresponding author
    1. Creative Research Institution, Hokkaido University, Sapporo 001-0021
      Authors to whom all correspondence should be addressed.
      Email: derek@res.agr.hokudai.ac.jp; jnakayam@cdb.riken.jp
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  • Jun-ichi Nakayama

    Corresponding author
    1. Laboratory for Chromatin Dynamics, RIKEN Center for Developmental Biology, Kobe, Hyogo 650-0047, Japan
      Authors to whom all correspondence should be addressed.
      Email: derek@res.agr.hokudai.ac.jp; jnakayam@cdb.riken.jp
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Authors to whom all correspondence should be addressed.
Email: derek@res.agr.hokudai.ac.jp; jnakayam@cdb.riken.jp

Abstract

Post-translational modifications of histones are critical not only for local regulation of gene expression, but also for higher-order structure of the chromosome and genome organization in general. These modifications enable a preset state to be maintained over subsequent generations and thus provide an epigenetic level of regulation. Heterochromatic regions of the genome are epigenetically regulated to maintain a “silent state” and protein coding genes inserted into these regions are subject to the same epigenetic silencing. The fission yeast Schizosaccharomyces pombe has well characterized regions of heterochromatin and has proven to be a powerful model for elucidation of epigenetic silencing mechanisms. Research in S. pombe led to the breakthrough discovery that epigenetic silencing is not solely a chromatin-driven transcriptional repression and that RNA interference of nascent transcripts can guide epigenetic silencing and associated histone modifications. Over the last 10 years, an eloquent integration of genetic and biochemical studies have greatly propelled our understanding of major players and effector complexes for regulation of RNAi-mediated epigenetic silencing in S. pombe. Here, we review recent research related to regulation of the epigenetic state in S. pombe heterochromatin, focusing specifically on the mechanisms by which transcription and RNA processing interact with the chromatin modification machinery to maintain the epigenetically silent state.

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