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American Association for the Advancement of Science, Science, 5935(324), p. 1716-1719, 2009

DOI: 10.1126/science.1172026

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Synthetic heterochromatin bypasses RNAi and centromeric repeats to establish functional centromeres

Journal article published in 2009 by Alexander A. Kagansky, Hernan H. Diego Folco, Hernan Diego Folco, Ricardo R. Almeida, Alison L. Pidoux, Abdelhalim Boukaba, Femke F. Simmer, Takeshi T. Urano, Georgina L. Hamilton, Robin C. Allshire ORCID
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This paper is available in a repository.

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Abstract

In the central domain of fission yeast centromeres, the kinetochore is assembled on CENP-A cnp1 nucleosomes. Normally, small interfering RNAs generated from flanking outer repeat transcripts direct histone H3 lysine 9 methyltransferase Clr4 to homologous loci to form heterochromatin. Outer repeats, RNA interference (RNAi), and centromeric heterochromatin are required to establish CENP-A Cnpl chromatin. We demonstrated that tethering Clr4 via DNA-binding sites at euchromatic loci induces heterochromatin assembly, with or without active RNAi. This synthetic heterochromatin completely substitutes for outer repeats on plasmid-based minichromosomes, promoting de novo CENP-A Cnpl and kinetochore assembly, to allow their mitotic segregation, even with RNAi inactive. Thus, the role of outer repeats in centromere establishment is simply the provision of RNAi substrates to direct heterochromatin formation; H3K9 methylation-dependent heterochromatin is alone sufficient to form functional centromeres. ; SCOPUS: ar.j ; info:eu-repo/semantics/published