Synthetic Heterochromatin Bypasses RNAi and Centromeric Repeats to Establish Functional Centromeres

Author:

Kagansky Alexander1,Folco Hernan Diego1,Almeida Ricardo1,Pidoux Alison L.1,Boukaba Abdelhalim1,Simmer Femke1,Urano Takeshi2,Hamilton Georgina L.1,Allshire Robin C.1

Affiliation:

1. Wellcome Trust Centre for Cell Biology, School of Biological Sciences, The University of Edinburgh, 6.34 Swann Building, Edinburgh EH9 3JR, Scotland, UK.

2. Department of Biochemistry, Shimane University Faculty of Medicine, 89-1 Enya-cho, Izumo 693-8501, Japan.

Abstract

Synthetic Centromere Every eukaryotic chromosome must have a centromere where the cell division machinery latches onto each chromosome pair to ensure an even apportioning of the genetic material between daughter cells. The characteristic (but not conserved) repeat sequences associated with most centromeres are thought to be required to induce an RNA interference (RNAi) response and thereby promote the formation of heterochromatin, needed for centromere function. Kagansky et al. (p. 1716 ) now show in fission yeast that these outer repeat sequences can be replaced in their entirety by very short sequences that recruit an enzyme, Clr4, which promotes the formation of heterochromatin in the absence of RNAi. Thus, flanking heterochromatin, regardless of its derivation, is all that is required for the formation of a functional centromere.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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