Section of Pediatric Infectious Disease, Department of Pediatrics, University of Chicago, Chicago, Illinois 60637, USA.
J Biol Chem. 2011 Jun 10;286(23):20977-90. doi: 10.1074/jbc.M111.230268. Epub 2011 Apr 12.
Eukaryotic cells utilize complex signaling systems to detect their environments, responding and adapting as new conditions arise during evolution. The basidiomycete fungus Cryptococcus neoformans is a leading cause of AIDS-related death worldwide and utilizes the calcineurin and protein kinase C-1 (Pkc1) signaling pathways for host adaptation and expression of virulence. In the present studies, a C-terminal zinc finger transcription factor, homologous both to the calcineurin-responsive zinc fingers (Crz1) of ascomycetes and to the Pkc1-dependent specificity protein-1 (Sp1) transcription factors of metazoans, was identified and named SP1 because of its greater similarity to the metazoan factors. Structurally, the Cryptococcus neoformans Sp1 (Cn Sp1) protein was found to have acquired an additional zinc finger motif from that of Crz1 and showed Pkc1-dependent phosphorylation, nuclear localization, and whole genome epistatic associations under starvation conditions. Transcriptional targets of Cn Sp1 shared functional similarities with Crz1 factors, such as cell wall synthesis, but gained the regulation of processes involved in carbohydrate metabolism, including trehalose metabolism, and lost others, such as the induction of autophagy. In addition, overexpression of Cn Sp1 in a pkc1Δ mutant showed restoration of altered phenotypes involved in virulence, including cell wall stability, nitrosative stress, and extracellular capsule production. Cn Sp1 was also found to be important for virulence of the fungus using a mouse model. In summary, these data suggest an evolutionary shift in C-terminal zinc finger proteins during fungal evolution, transforming them from calcineurin-dependent to PKC1-dependent transcription factors, helping to shape the role of fungal pathogenesis of C. neoformans.
真核细胞利用复杂的信号系统来感知其环境,在进化过程中,当出现新的情况时,它们会做出反应并适应。担子菌真菌新生隐球菌是全球艾滋病相关死亡的主要原因,它利用钙调神经磷酸酶和蛋白激酶 C-1(Pkc1)信号通路来适应宿主和表达毒力。在本研究中,鉴定并命名了一种 C 端锌指转录因子,它与子囊菌的钙调神经磷酸酶反应性锌指(Crz1)同源,与后生动物的 Pkc1 依赖性特异性蛋白-1(Sp1)转录因子同源,因其与后生动物因子的相似性更大而得名 Sp1。结构上,发现新生隐球菌 Sp1(Cn Sp1)蛋白从 Crz1 获得了额外的锌指结构,并显示出 Pkc1 依赖性磷酸化、核定位以及在饥饿条件下的全基因组上位性关联。Cn Sp1 的转录靶标与 Crz1 因子具有相似的功能,如细胞壁合成,但获得了参与碳水化合物代谢的过程的调节,包括海藻糖代谢,并失去了其他过程,如自噬的诱导。此外,在 pkc1Δ突变体中过表达 Cn Sp1 显示出恢复了与毒力相关的表型改变,包括细胞壁稳定性、硝化应激和细胞外荚膜产生。在使用小鼠模型时,还发现 Cn Sp1 对真菌的毒力也很重要。总之,这些数据表明,在真菌进化过程中,C 端锌指蛋白发生了进化转变,从钙调神经磷酸酶依赖性转变为 PKC1 依赖性转录因子,有助于塑造新生隐球菌真菌发病机制的作用。