The Complete Set of Predicted Genes from Saccharomyces cerevisiae in a Readily Usable Form

  1. James R. Hudson, Jr.1,
  2. Elliott P. Dawson2,
  3. Kimberly L. Rushing1,
  4. Cynthia H. Jackson1,
  5. Daniel Lockshon3,
  6. Diana Conover3,
  7. Christian Lanciault3,
  8. James R. Harris2,
  9. Steven J. Simmons2,
  10. Rodney Rothstein4, and
  11. Stanley Fields3,5
  1. 1Research Genetics Inc., Huntsville, Alabama 35801; 2BioVentures, Inc., Mufreesboro, Tennessee 37129; 3Departments of Genetics and Medicine, University of Washington, Seattle, Washington 98195; 4Department of Genetics and Development, Columbia University, New York, New York 10032

Abstract

Nearly all of the open reading frames (ORFs) of the yeastSaccharomyces cerevisiae have been synthesized by PCR using a set of ∼6000 primer pairs. Each of the forward primers has a common 22-base sequence at its 5′ end, and each of the back primers has a common 20-base sequence at its 5′ end. These common termini allow reamplification of the entire set of original PCR products using a single pair of longer primers—in our case, 70 bases. The resulting 70-base elements that flank each ORF can be used for rapid and efficient cloning into a linearized yeast vector that contains these same elements at its termini. This cloning by genetic recombination obviates the need for ligations or bacterial manipulations and should permit convenient global approaches to gene function that require the assay of each putative yeast gene.

Footnotes

  • 5 Corresponding author.

  • E-MAIL fields{at}genetics.washington.edu; FAX (206) 543-0754.

    • Received July 7, 1997.
    • Accepted October 17, 1997.
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