A multicopy suppressor of a cell cycle defect in S. pombe encodes a heat shock‐inducible 40 kDa cyclophilin‐like protein

• Published in: The EMBO journal Vol. 15; no. 3; pp. 447 - 456
• Main Authors: Weisman, R., Creanor, J., Fantes, P.
• Format: Journal Article
• Language: English
• Published: England 01.02.1996
• Subjects: Amino Acid Isomerases - biosynthesis; Amino Acid Isomerases - chemistry; Amino Acid Isomerases - genetics; Amino Acid Sequence; Animals; Base Sequence; Carrier Proteins - biosynthesis; Carrier Proteins - chemistry; Carrier Proteins - genetics; Cell Cycle - genetics; DNA, Fungal - genetics; Fungal Proteins - biosynthesis; Fungal Proteins - chemistry; Fungal Proteins - genetics; Genes, Fungal; Genes, Suppressor; Hot Temperature; Humans; Molecular Sequence Data; Molecular Weight; Multigene Family; Mutagenesis, Site-Directed; Peptidylprolyl Isomerase; Restriction Mapping; RNA, Messenger - genetics; RNA, Messenger - metabolism; Schizosaccharomyces - genetics; Schizosaccharomyces - metabolism; Schizosaccharomyces pombe; Sequence Homology, Amino Acid
• ISSN: 0261-4189; 1460-2075
• DOI: 10.1002/j.1460-2075.1996.tb00377.x

Cyclophilins are peptidyl‐prolyl cis‐trans isomerases (PPIases) which have been implicated in intracellular protein folding, transport and assembly. Cyclophilins are also known as the intracellular receptors for the immunosuppressive drug cyclosporin A (CsA). The most common type of cyclophilins are the 18 kDa cytosolic proteins containing only the highly conserved core domain for PPIase and CsA binding activities. The wis2+ gene of the fission yeast Schizosaccharomyces pombe was isolated as a multicopy suppressor of wee1–50 cdc25–22 win1–1, a triple mutant strain which exhibits a cell cycle defect phenotype. Sequence analysis of wis2+ reveals that it encodes a 40 kDa cyclophilin‐like protein, homologous to the mammalian cyclophilin 40. The 18 kDa cyclophilin domain (CyP‐18) of wis2 is followed by a C‐terminal region of 188 amino acids. The C‐terminal region of wis2 is essential for suppression of the triple mutant defect. Furthermore this region of the protein is able to confer suppression activity on the 18 kDa S.pombe cyclophilin, cyp1, since a hybrid protein consisting of an 18 kDa S.pombe cyclophilin (cyp1) fused to the C‐terminus of wis2 shows suppression activity. We also demonstrate that the level of wis2+ mRNA increases 10‐ to 20‐fold upon heat shock of S.pombe cells suggesting a role for wis2+ in the heat‐shock response.