Teunissen A W, van den Berg J A, Steensma H Y
Leiden University, Institute of Molecular Plant Sciences, The Netherlands.
Yeast. 1995 Jun 30;11(8):735-45. doi: 10.1002/yea.320110805.
In the yeast Saccharomyces cerevisiae three dominant flocculation genes, FLO1, FLO5 and FLO8 have been described. Until now only the FLO1 gene, which is located at chromosome I, has been cloned and sequenced. FLO5 and FLO8 were previously localized at chromosomes I and VIII respectively (Vezinhet, F., Blondin, B. and Barre, P. (1991). Mapping of the FLO5 gene of Saccharomyces cerevisiae by transfer of a chromosome during cytoduction. Biotechnol. Lett. 13, 47-52; Yamashita, I. and Fukui, S. (1983). Mating signals control expression of both starch fermentation genes and a novel flocculation gene FLO8 in the yeast Saccharomyces. Agric. Biol. Chem. 47, 2889-2896). This was not in agreement with our results. Here, we report the location of FLO5 and FLO8 on chromosomes VIII and I respectively. By induced chromosome loss and genetic mapping, the FLO5 gene was localized at the right end of chromosome VIII approximately 34 cM centromere distal of PET3. This is part of the region that is present both at chromosome I and chromosome VIII. The location of FLO5 in this area of chromosome VIII made it necessary to re-evaluate the localization of FLO8, which was previously thought to occur in this region. Both genetic and physical mapping showed that FLO8 is allelic to FLO1. Hence, there are only two known dominant flocculation genes, FLO1 and FLO5. Analysis of the nucleotide sequence of chromosome VIII of a non-flocculent strain revealed an open reading frame encoding a putative protein that is approximately 96% identical to the Flo1 protein. This suggests that both dominant flocculation genes encode similar, cell wall-associated, proteins with the same function in the flocculation mechanism.
在酿酒酵母中,已发现三个显性絮凝基因FLO1、FLO5和FLO8。到目前为止,只有位于1号染色体上的FLO1基因被克隆和测序。FLO5和FLO8之前分别定位在1号和8号染色体上(Vezinhet, F., Blondin, B.和Barre, P.(1991年)。通过细胞融合过程中染色体的转移对酿酒酵母FLO5基因进行定位。生物技术快报。13, 47 - 52;Yamashita, I.和Fukui, S.(1983年)。交配信号控制酵母酿酒酵母中淀粉发酵基因和一个新的絮凝基因FLO8的表达。农业生物化学。47, 2889 - 2896)。这与我们的结果不一致。在这里,我们报告FLO5和FLO8分别位于8号和1号染色体上。通过诱导染色体丢失和遗传定位,FLO5基因定位在8号染色体的右端,距PET3着丝粒约34 cM远。这是1号和8号染色体上都存在的区域的一部分。FLO5在8号染色体的这个区域的定位使得有必要重新评估FLO8的定位,FLO8之前被认为位于这个区域。遗传和物理定位都表明FLO8与FLO1等位。因此,已知的显性絮凝基因只有两个,FLO1和FLO5。对一个非絮凝菌株的8号染色体核苷酸序列分析揭示了一个开放阅读框,其编码一种假定的蛋白质,该蛋白质与Flo1蛋白约96%相同。这表明两个显性絮凝基因编码在絮凝机制中具有相同功能的相似的、与细胞壁相关的蛋白质。