Subnuclear relocalization and silencing of a chromosomal region by an ectopic ribosomal DNA repeat

Tadas Jakociunas, Marie Elise Domange Jordö, Mazhoura Aït Mebarek, Camilla Marie Bünner, Janne Verhein Hansen, Lene Broeng Oddershede, Genevieve Thon

14 Citationer (Scopus)

Abstract

Our research addresses the relationship between subnuclear localization and gene expression in fission yeast. We observed the relocalization of a heterochromatic region, the mating-type region, from its natural location at the spindle-pole body to the immediate vicinity of the nucleolus. Relocalization occurred in response to a DNA rearrangement replacing a boundary element (IR-R) with a ribosomal DNA repeat (rDNA-R). Gene expression was strongly silenced in the relocalized mating-type region through mechanisms that differ from those operating in wild type. Also different from the wild-type situation, programmed recombination events failed to take place in the rDNA-R mutant. Increased silencing and perinucleolar localization depended on Reb1, a DNA-binding protein with cognate sites in the rDNA. Reb1 was recently shown to mediate long-range interchromosomal interactions in the nucleus through dimerization, providing a mechanism for the observed relocalization. Replacing the full rDNA repeat with Reb1-binding sites, and using mutants lacking the histone H3K9 methyltransferase Clr4, indicated that the relocalized region was silenced redundantly by heterochromatin and another mechanism, plausibly antisense transcription, achieving a high degree of repression in the rDNA-R strain.
OriginalsprogEngelsk
TidsskriftProceedings of the National Academy of Sciences of the United States of America
Vol/bind110
Udgave nummer47
Sider (fra-til)E4465-E4473
Antal sider9
ISSN0027-8424
DOI
StatusUdgivet - 19 nov. 2013

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