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Molecular and Cellular Biology, February 2009, p. 835-848, Vol. 29, No. 3
0270-7306/09/$08.00+0 doi:10.1128/MCB.01009-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Laboratoire de Biologie Moléculaire Eucaryote, Université de Toulouse, 118 Route de Narbonne, F-31062 Toulouse, France,1 UMR5099, CNRS, IFR109, Toulouse, France,2 Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, CH-4058 Basel, Switzerland,3 Leiden University Medical Center, Department of Toxicogenetics, Einthovenweg 20, 2333 ZC, Leiden, The Netherlands4
Received 26 June 2008/ Returned for modification 23 July 2008/ Accepted 18 November 2008
We have examined the hypothesis that the highly selective recombination of an active mating type locus (MAT) with either HML
or HMRa is facilitated by the spatial positioning of relevant sequences within the budding yeast (Saccharomyces cerevisiae) nucleus. However, both position relative to the nuclear envelope (NE) and the subnuclear mobility of fluorescently tagged MAT, HML, or HMR loci are largely identical in haploid a and
cells. Irrespective of mating type, the expressed MAT locus is highly mobile within the nuclear lumen, while silent loci move less and are found preferentially near the NE. The perinuclear positions of HMR and HML are strongly compromised in strains lacking the Silent information regulator, Sir4. However, HML
, unlike HMRa and most telomeres, shows increased NE association in a strain lacking yeast Ku70 (yKu70). Intriguingly, we find that the yKu complex is associated with HML and HMR sequences in a mating-type-specific manner. Its abundance decreases at the HML
donor locus and increases transiently at MATa following DSB induction. Our data suggest that mating-type-specific binding of yKu to HML
creates a local chromatin structure competent for recombination, which cooperates with the recombination enhancer to direct donor choice for gene conversion of the MATa locus.
Published ahead of print on 1 December 2008.
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