Isolation of a Trichoderma reesei cDNA encoding GTP: a-d-mannose-1-phosphate guanyltransferase involved in early steps of protein glycosylation |
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Authors: | Joanna S. Kruszewska Markku Saloheimo Merja Penttilä Grażyna Palamarczyk |
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Affiliation: | (1) Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawin′skiego 5 a, 02 106 Warsaw, Poland, PL;(2) VTT Biotechnology and Food Research, P. O. Box 1500, FIN-02044 VTT, Finland, FI |
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Abstract: | A cDNA coding for GTP: α-d-mannose-1-phosphate guanyltransferase (MPG1 transferase) (EC 2.7.7.13) was isolated from a cDNA library of the Trichoderma reesei RutC-30 strain by suppression of the yeast Saccharomyces cerevisiae mutation in the DPM1gene encoding mannosylphosphodolichol (MPD) synthase. The nucleotide sequence of the 1.6 kb-long cDNA revealed an ORF which encodes a protein of 364 amino acids. Sequence comparisons demonstrate 70% identity with the S. cerevisiae guanyl transferase gene (MPG1) and 75% identity with the Schizosaccharomyces pombe homologue. No similarity was found with the MPD synthase encoded by the S. cerevisiae DPM1 gene. The possibility that cloned cDNA encodes a product with a MPD synthase activity was also excluded by transforming a heterozygous S. cerevisiae dpm1::LEU2/DPM1 diploid, which did not lead to the restoration of viability of the dpm1 spores. Simultaneously, a significant increase in MPG transferase activity, as compared with the wild-type yeast, was observed in cellular extracts when the mpg1 cDNA from Trichoderma was expressed in the S. cerevisiae dpm1-6 mutant. Received: 21 July 1997 / 24 April 1998 |
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Keywords: | Trichoderma reesei GTP:α -d-mannose-1-phosphate guanyltransferase S. cerevisiae dpm1 mutant mpg1 gene Glycosylation |
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