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酵母DNA与草履虫副融合蛋白及不同磷酸葡萄糖变位酶特异性探针的比较杂交分析。

A comparative hybridization analysis of yeast DNA with Paramecium parafusin- and different phosphoglucomutase-specific probes.

作者信息

Wyroba E, Satir B H

机构信息

Department of Cell Biology, Nencki Institute of Experimental Biology, Warsaw, Poland.

出版信息

Biochem Cell Biol. 2000;78(6):683-90.

Abstract

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.

摘要

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。

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