Saccharomyces forkhead protein Fkh1 regulates donor preference during mating-type switching through the recombination enhancer

  1. Kaiming Sun1,
  2. Eric Coı̈c1,
  3. Zhiqi Zhou1,
  4. Pascal Durrens2, and
  5. James E. Haber1,3
  1. 1Rosenstiel Center and Department of Biology, Brandeis University, Waltham, Massachusetts 02254-9910, USA; 2Center of Bioinformatics of Bordeaux, University of Bordeaux 2, 33076 Bordeaux cedex, France

Abstract

Saccharomyces mating-type switching results from replacement by gene conversion of the MAT locus with sequences copied from one of two unexpressed donor loci, HML or HMR. MATa cells recombine with HMLα ∼90% of the time, whereas MATα cells choose HMRa 80%–90% of the time. HML preference in MATa is controlled by the cis-acting recombination enhancer (RE) that regulates recombination along the entire left arm of chromosome III. Comparison of RE sequences between S. cerevisiae, S. carlsbergensis, and S. bayanus defines four highly conserved regions (A, B, C, and D) within a 270-bp minimum RE. An adjacent E region enhances RE activity. Multimers of region A, D, or E are sufficient to promote selective use of HML. Regions A, D, and E each bind in vivo the transcription activator forkhead proteins Fkh1p and Fkh2p and their associated Ndd1p, although there are no adjacent open reading frames (ORFs). Deletion of FKH1significantly reduces MATa's use of HML, as does mutation of the Fkh1/Fkh2-binding sites in a multimer of region A. We conclude that Fkh1p regulates MATa donor preference through direct interaction with RE.

Keywords

Footnotes

  • 3 Corresponding author.

  • E-MAIL haber{at}brandeis.edu; FAX (781) 736-2405.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.994902.

    • Received April 4, 2002.
    • Accepted June 18, 2002.
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