Expansion and contraction of ribosomal DNA repeats in Saccharomyces cerevisiae: requirement of replication fork blocking (Fob1) protein and the role of RNA polymerase I

  1. Takehiko Kobayashi1,
  2. Denis J. Heck2,3,
  3. Masayasu Nomura2, and
  4. Takashi Horiuchi1,4
  1. 1National Institute for Basic Biology, Myodaijicho, Okazaki, 444-8585, Japan; 2Department of Biological Chemistry, University of California–Irvine, Irvine, California 92697-1700 USA

Abstract

Saccharomyces cerevisiae carries ∼150 copies of rDNA in tandem repeats. It was found that the absence of an essential subunit of RNA polymerase I (Pol I) in rpa135 deletion mutants triggers a gradual decrease in rDNA repeat number to about one-half the normal level. Reintroduction of the missing RPA135 gene induced a gradual increase in repeat number back to the normal level. GeneFOB1 was shown to be essential for both the decrease and increase of rDNA repeats. FOB1 was shown previously to be required for replication fork blocking (RFB) activity at RFBsite in rDNA and for recombination hot-spot (HOT1) activity. Thus, DNA replication fork blockage appears to stimulate recombination and play an essential role in rDNA expansion/contraction and sequence homogenization, and possibly, in the instability of repeated sequences in general. RNA Pol I, on the other hand, appears to control repeat numbers, perhaps by stabilizing rDNA with the normal repeat numbers as a stable nucleolar structure.

Keywords

Footnotes

  • 3 Present address: Beckman Coulter, Inc., Fullerton, California 92834-3100 USA.

  • 4 Corresponding author.

  • E-MAIL kishori{at}nibb.ac.jp; FAX 81-564-55-7690.

    • Received September 28, 1998.
    • Accepted November 3, 1998.
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