Farley F W, Satterberg B, Goldsmith E J, Elion E A
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genetics. 1999 Apr;151(4):1425-44. doi: 10.1093/genetics/151.4.1425.
Fus3p and Kss1p act at the end of a conserved signaling cascade that mediates numerous cellular responses for mating. To determine the role of Fus3p in different outputs, we isolated and characterized a series of partial-function fus3 point mutants for their ability to phosphorylate a substrate (Ste7p), activate Ste12p, undergo G1 arrest, form shmoos, select partners, mate, and recover. All the mutations lie in residues that are conserved among MAP kinases and are predicted to affect either enzyme activity or binding to Ste7p or substrates. The data argue that Fus3p regulates the various outputs assayed through the phosphorylation of multiple substrates. Different levels of Fus3p function are required for individual outputs, with the most function required for shmoo formation, the terminal output. The ability of Fus3p to promote shmoo formation strongly correlates with its ability to promote G1 arrest, suggesting that the two events are coupled. Fus3p promotes recovery through a mechanism that is distinct from its ability to promote G1 arrest and may involve a mechanism that does not require kinase activity. Moreover, catalytically inactive Fus3p inhibits the ability of active Fus3p to activate Ste12p and hastens recovery without blocking G1 arrest or shmoo formation. These results raise the possibility that in the absence of sustained activation of Fus3p, catalytically inactive Fus3p blocks further differentiation by restoring mitotic growth. Finally, suppression analysis argues that Kss1p contributes to the overall pheromone response in a wild-type strain, but that Fus3p is the critical kinase for all of the outputs tested.
Fus3p和Kss1p作用于一条保守信号级联反应的末端,该级联反应介导了众多与交配相关的细胞反应。为了确定Fus3p在不同输出中的作用,我们分离并鉴定了一系列部分功能的fus3点突变体,测定了它们磷酸化底物(Ste7p)、激活Ste12p、导致G1期停滞、形成接合芽、选择交配伙伴、进行交配以及恢复的能力。所有突变均位于丝裂原活化蛋白激酶(MAP激酶)中保守的残基上,预计会影响酶活性或与Ste7p或底物的结合。数据表明,Fus3p通过对多种底物的磷酸化来调节所检测的各种输出。不同的输出需要不同水平的Fus3p功能,其中形成接合芽(最终输出)需要的功能最多。Fus3p促进接合芽形成的能力与其促进G1期停滞的能力密切相关,表明这两个事件是相互关联的。Fus3p通过一种与其促进G1期停滞的能力不同的机制促进恢复,这种机制可能涉及一种不需要激酶活性的机制。此外,催化失活的Fus3p会抑制活性Fus3p激活Ste12p的能力,并加速恢复,而不会阻止G1期停滞或接合芽形成。这些结果提出了一种可能性,即在没有Fus3p持续激活的情况下,催化失活的Fus3p通过恢复有丝分裂生长来阻止进一步分化。最后,抑制分析表明,在野生型菌株中Kss1p对整体信息素反应有贡献,但Fus3p是所有测试输出的关键激酶。