Degenerate oligonucleotide probes encoding sequences conserved among mammalian protein-tyrosine-phosphatases (PTPases) were used to amplify DNA fragments from a Schizosaccharomyces pombe cDNA library by polymerase chain reaction (PCR) methods. A cloned PCR product predicted peptide sequences similar to those found in PTPases but not identical to any published sequences. A S. pombe gene, designated pypl+, was identified in a cDNA library with this PCR probe, cloned, and sequenced. The sequence of the gene predicted a 550-amino acid protein with M(r) 61,586, which includes amino acid sequences that are highly conserved in mammalian PTPases. Disruption of the pypl+ gene resulted in viable cells. Overexpression of the pypl+ gene in S. pombe permitted detection of a protein of apparent M(r) 63,000.