Teunissen A W, van den Berg J A, Steensma H Y
Department of Microbiology and Enzymology, Delft University of Technology, The Netherlands.
Yeast. 1993 Jan;9(1):1-10. doi: 10.1002/yea.320090102.
The genetics of flocculation in the yeast Saccharomyces cerevisiae are poorly understood despite the importance of this property for strains used in industry. To be able to study the regulation of flocculation in yeast, one of the genes involved, FLO1, has been partially cloned. The identity of the gene was confirmed by the non-flocculent phenotype of cells in which the C-terminal part of the gene had been replaced by the URA3 gene. Southern blots and genetic crosses showed that the URA3 gene had integrated at the expected position on chromosome I. A region of approximately 2 kb in the middle of the FLO1 gene was consistently deleted during propagation in Escherichia coli and could not be isolated. Plasmids containing the incomplete gene, however, were still able to cause weak flocculation in a non-flocculent strain. The 3' end of the FLO1 gene was localized at approximately 24 kb from the right end of chromosome I, 20 kb centromere-proximal to PHO11. Most of the newly isolated chromosome I sequences also hybridized to chromosome VIII DNA, thus extending the homology between the right end of chromosome I and chromosome VIII to approximately 28 kb.
尽管絮凝特性对工业用酵母菌株很重要,但酿酒酵母中絮凝的遗传学仍未得到充分理解。为了能够研究酵母中絮凝的调控,其中一个相关基因FLO1已被部分克隆。通过将该基因的C末端部分替换为URA3基因的细胞的非絮凝表型,证实了该基因的身份。Southern杂交和遗传杂交表明URA3基因已整合到染色体I上的预期位置。在大肠杆菌中繁殖期间,FLO1基因中间约2kb的区域持续缺失,无法分离。然而,含有不完整基因的质粒仍能够在非絮凝菌株中引起弱絮凝。FLO1基因的3'端位于距染色体I右端约24kb处,着丝粒近端距PHO11 20kb。大多数新分离的染色体I序列也与染色体VIII DNA杂交,从而将染色体I右端与染色体VIII之间的同源性扩展到约28kb。