Affiliation:
1. Department of Biology and Curriculum in Genetics and Molecular Biology 1 and
2. The Lineberger Comprehensive Cancer Center, 2 University of North Carolina, Chapel Hill, North Carolina 27599-3280, and
3. Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey 088543
Abstract
ABSTRACT
Tandem repeats of the pentanucleotide 5′-CCGNN (where N indicates any base) were previously shown to exclude nucleosomes in vitro (Y.-H. Wang and J. D. Griffith, Proc. Natl. Acad. Sci. USA 93:8863–8867, 1996). To determine the in vivo effects of these sequences, we replaced the upstream regulatory sequences of the
HIS4
gene of
Saccharomyces cerevisiae
with either 12 or 48 tandem copies of CCGNN. Both tracts activated
HIS4
transcription. We found that (CCGNN)
12
tracts elevated meiotic recombination (hot spot activity), whereas the (CCGNN)
48
tract repressed recombination (cold spot activity). In addition, a “pure” tract of (CCGAT)
12
activated both transcription and meiotic recombination. We suggest that the cold spot activity of the (CCGNN)
48
tract is related to the phenomenon of the suppressive interactions of adjacent hot spots previously described in yeast (Q.-Q. Fan, F. Xu, and T. D. Petes, Mol. Cell. Biol. 15:1679–1688, 1995; Q.-Q. Fan, F. Xu, M. A. White, and T. D. Petes, Genetics 145:661–670, 1997; T.-C. Wu and M. Lichten, Genetics 140:55–66, 1995; L. Xu and N. Kleckner, EMBO J. 16:5115–5128, 1995).
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
57 articles.
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