Tekinay Turgay, Ennis Herbert L, Wu Mary Y, Nelson Margaret, Kessin Richard H, Ratner David I
Department of Anatomy and Cell Biology, Columbia University, New York, New York 10032, USA.
Eukaryot Cell. 2003 Jun;2(3):618-26. doi: 10.1128/EC.2.3.618-626.2003.
Dictyostelium discoideum amoebae with an altered fbxA gene, which is thought to encode a component of an SCF E3 ubiquitin ligase, have defective regulation of cell type proportionality. In chimeras with wild-type cells, the mutant amoebae form mainly spores, leaving the construction of stalks to wild-type cells. To examine the role of fbxA and regulated proteolysis, we have recovered the promoter of fbxA and shown that it is expressed in a pattern resembling that of a prestalk-specific gene until late in development, when it is also expressed in developing spore cells. Because fbxA cells are developmentally deficient in pure culture, we were able to select suppressor mutations that promote sporulation of the original mutant. One suppressor mutation resides within the gene regA, which encodes a cyclic AMP (cAMP) phosphodiesterase linked to an activating response regulator domain. In another suppressor, there has been a disruption of dhkA, a gene encoding a two-component histidine kinase known to influence Dictyostelium development. RegA appears precociously and in greater amounts in the fbxA mutant than in the wild type, but in an fbxA/dhkA double mutant, RegA is restored to wild-type levels. Because the basis of regA suppression might involve alterations in cAMP levels during development, the concentrations of cAMP in all strains were determined. The levels of cAMP are relatively constant during multicellular development in all strains except the dhkA mutant, in which it is reduced at least sixfold. The level of cAMP in the double mutant dhkA/fbxA is relatively normal. The levels of cAMP in the various mutants do not correlate with spore formation, as would be expected on the basis of our present understanding of the signaling pathway leading to the induction of spores. Altered amounts of RegA and cAMP early in the development of the mutants suggest that both fbxA and dhkA genes act earlier than previously thought.
盘基网柄菌(Dictyostelium discoideum)中,fbxA基因发生改变的变形虫,被认为编码SCF E3泛素连接酶的一个组分,其细胞类型比例调节存在缺陷。在与野生型细胞形成的嵌合体中,突变变形虫主要形成孢子,而将柄的构建留给野生型细胞。为了研究fbxA的作用和受调控的蛋白水解,我们获得了fbxA的启动子,并表明其表达模式类似于前柄特异性基因,直到发育后期,此时它也在发育中的孢子细胞中表达。由于fbxA细胞在纯培养中发育缺陷,我们能够选择促进原始突变体孢子形成的抑制突变。一个抑制突变位于regA基因内该基因编码一种与激活反应调节域相连的环磷酸腺苷(cAMP)磷酸二酯酶。在另一个抑制突变中,dhkA基因发生了破坏,dhkA是一个编码双组分组氨酸激酶的基因,已知其会影响盘基网柄菌的发育。RegA在fbxA突变体中比在野生型中更早且大量出现,但在fbxA/dhkA双突变体中,RegA恢复到野生型水平。由于regA抑制的基础可能涉及发育过程中cAMP水平的改变,因此测定了所有菌株中cAMP的浓度。除dhkA突变体中cAMP水平至少降低六倍外,所有菌株在多细胞发育过程中cAMP水平相对恒定。双突变体dhkA/fbxA中的cAMP水平相对正常。各种突变体中cAMP的水平与孢子形成不相关,这与我们目前对导致孢子诱导的信号通路的理解预期一致。突变体发育早期RegA和cAMP量的改变表明fbxA和dhkA基因的作用比之前认为的更早。