Wyroba E, Satir B H
Department of Cell Biology, Nencki Institute of Experimental Biology, Warsaw, Poland.
Biochem Cell Biol. 2000;78(6):683-90.
Molecular probes designed for the parafusin (PFUS), the Paramecium exocytic-sensitive phosphoglycoprotein, 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--I-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.
与不同的磷酸葡萄糖变位酶特异性探针相比,为草履虫胞吐敏感磷酸糖蛋白副融合蛋白(PFUS)设计的分子探针在酿酒酵母基因组DNA中呈现出不同的杂交模式。这些探针包括两个与酵母磷酸葡萄糖变位酶(PGM)基因1和2的片段相同的探针。PGM探针均未在经Bgl II切割的酵母DNA消化产物中检测到用1.6 kb克隆的PFUS cDNA和针对PFUS区域构建的寡核苷酸(插入片段3 - I - 3)所检测到的7.4 kb和5.9 kb片段,这些片段在其他物种中未发现。用PFUS特异性引物进行PCR扩增产生了预测分子大小的酵母DNA片段,这些片段与I - 3探针杂交。对酵母基因组数据库的搜索产生了一个未指定的核苷酸序列,该序列在扩增区域内与副融合蛋白基因有55%的同一性,与PGM2(酵母磷酸葡萄糖变位酶的主要同工型)有37%的同一性。