Ramezani Rad M, Jansen G, Bühring F, Hollenberg C P
Institut für Mikrobiologie, Heinrich-Heine-Universität Düsseldorf, Germany.
Mol Gen Genet. 1998 Jul;259(1):29-38. doi: 10.1007/s004380050785.
STE50 is required to sustain pheromone-induced signal transduction in S. cerevisiae. Here we report that Ste50p is involved in regulating pseudohyphal development. Both of these processes are also dependent on Ste11p. Deletion of STE50 leads to defects in filamentous growth, which can be suppressed by overproduction of Ste11p. Overexpression of STE11 also suppresses the mating defects of ste50 mutants. We have analysed the physical association between Ste50p and Ste11p in extracts of cells harvested under various conditions. A Ste11p-Ste50p complex can be isolated from extracts of cells in which the pheromone response has been activated, as well as from normally growing cells. Formation of the Ste50p-Ste11p complex does not require G(alpha), G(beta), Ste20p or Ste5p. Oligomerisation of Ste11p is shown to be independent of activation of the pheromone response pathway, and occurs in the absence of Ste50p. We conclude that Ste50p is necessary for Ste11p activity in at least two differentiation programmes: mating and filamentous growth.
STE50是酿酒酵母中维持信息素诱导的信号转导所必需的。在此我们报告Ste50p参与调节假菌丝发育。这两个过程也都依赖于Ste11p。STE50的缺失导致丝状生长缺陷,而Ste11p的过量表达可以抑制该缺陷。STE11的过表达也能抑制ste50突变体的交配缺陷。我们分析了在各种条件下收获的细胞提取物中Ste50p和Ste11p之间的物理关联。可以从信息素反应已被激活的细胞提取物以及正常生长的细胞提取物中分离出Ste11p - Ste50p复合物。Ste50p - Ste11p复合物的形成不需要G(α)、G(β)、Ste20p或Ste5p。已表明Ste11p的寡聚化独立于信息素反应途径的激活,并且在没有Ste50p的情况下发生。我们得出结论,在至少两个分化程序中,即交配和丝状生长中,Ste50p对于Ste11p的活性是必需的。