Bidard F, Blondin B, Dequin S, Vezinhet F, Barre P
Laboratoire de Microbiologie et Technologie des Fermentations, Institut des Produits de la Vigne (I.P.V.), INRA, Montpellier, France.
Curr Genet. 1994 Mar;25(3):196-201. doi: 10.1007/BF00357162.
A yeast flocculation gene was isolated from a genomic library of an FLO5 strain of S. cerevisiae on the basis of its ability to trigger flocculation in a non-flocculent strain. Characterization of the cloned gene by restriction mapping, Southern analysis, and chromosome mapping have shown that it corresponds to a FLO5 gene previously located on chromosome I and that this gene is related to the already described FLO1 gene. A study of gene expression in different yeast strains has indicated that, while this gene is dominant, its expression can be suppressed in some genetic backgrounds. A Northern-blot analysis has demonstrated that the same 5000-nt transcript was present in an FLO5 and an FLO1 strain. A gene disruption experiment has led to the conclusion that another flocculation gene is present and can be active in the FLO5 strain we used.
基于其在非絮凝菌株中引发絮凝的能力,从酿酒酵母FLO5菌株的基因组文库中分离出一个酵母絮凝基因。通过限制性图谱分析、Southern分析和染色体定位对克隆基因进行表征,结果表明它对应于先前位于I号染色体上的FLO5基因,且该基因与已描述的FLO1基因相关。对不同酵母菌株中基因表达的研究表明,虽然该基因具有显性,但在某些遗传背景下其表达可能会受到抑制。Northern印迹分析表明,FLO5和FLO1菌株中存在相同的5000 nt转录本。基因破坏实验得出结论,我们使用的FLO5菌株中存在另一个絮凝基因且该基因可能具有活性。