Abstract
Molecular probes designed for the parafusin (PFUS), the Paramecium exocytic-sensitive phosphoglyco-protein, gave distinct hybridization patterns in Saccharomyces cerevisiae genomic DNA when compared with different phosphoglucomutase specific probes. These include two probes identical to segments of yeast phosphoglucomutase (PGM) genes 1 and 2. Neither of the PGM probes revealed the 7.4 and 5.9 kb fragments in Bgl II-cut yeast DNA digest detected with the 1.6 kb cloned PFUS cDNA and oligonucleotide constructed to the PFUS region (insertion 3 -1-3) not found in other species. PCR amplification with PFUS-specific primers generated yeast DNA-species of the predicted molecular size which hybridized to the I-3 probe. A search of the yeast genome database produced an unassigned nucleotide sequence that showed 55% identity to parafusin gene and 37% identity to PGM2 (the major isoform of yeast phosphoglucomutase) within the amplified region.
Original language | English (US) |
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Pages (from-to) | 683-690 |
Number of pages | 8 |
Journal | Biochemistry and Cell Biology |
Volume | 78 |
Issue number | 6 |
DOIs | |
State | Published - Dec 1 2000 |
Keywords
- Hybridization
- PCR
- Parafusin
- Phosphoglucomutase
- Yeast
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology