Bruni Gillian O, Battle Blake, Kelly Ben, Zhang Zhengguang, Wang Ping
Department of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, LA, United States of America.
College of Arts and Sciences, Loyola University New Orleans, New Orleans, LA, United States of America.
PLoS One. 2017 Jul 7;12(7):e0180243. doi: 10.1371/journal.pone.0180243. eCollection 2017.
Cryptococcus neoformans causes often-fatal fungal meningoencephalitis in immunocompromised individuals. While the exact disease mechanisms remain elusive, signal transduction pathways mediated by key elements such as G-protein α subunit Gpa1, small GTPase Ras1, and atypical Gβ-like/RACK1 protein Gib2 are known to play important roles in C. neoformans virulence. Gib2 is important for normal growth, differentiation, and pathogenicity, and it also positively regulates cAMP levels in conjunction with Gpa1. Interestingly, Gib2 displays a scaffold protein property by interacting with a wide variety of cellular proteins. To explore Gib2 global regulatory functions, we performed two-dimensional differential gel electrophoresis (DIGE) analysis and found that GIB2 disruption results in an increased expression of 304 protein spots (43.4%) and a decreased expression of 396 protein spots (56.6%). Analysis of 96 proteins whose expression changes were deemed significant (≥ +/- 1.5- fold) revealed that 75 proteins belong to at least 12 functional protein groups. Among them, eight groups have the statistical stringency of p ≤ 0.05, and four groups, including Hsp70/71 heat shock protein homologs and ribosomal proteins, survived the Bonferroni correction. This finding is consistent with earlier established roles for the human Gβ-like/RACK1 and the budding yeast Saccharomyces cerevisiae Asc1. It suggests that Gib2 could also be part of the complex affecting ribosomal biogenesis and protein translation in C. neoformans. Since eukaryotic Hsp70/71 proteins are involved in the facilitation of nascent protein folding, processing, and protection of cells against stress, we also propose that Gib2-regulated stress responses are linked to fungal virulence. Collectively, our study supports a conserved role of Gβ-like/RACK/Gib2 proteins in the essential cellular process of ribosomal biogenesis and protein translation. Our study also highlights a multifaceted regulatory role of Gib2 in the growth and pathogenicity of C. neoformans.
新型隐球菌可在免疫功能低下的个体中引发常为致命性的真菌性脑膜脑炎。虽然确切的发病机制仍不清楚,但已知由关键元件介导的信号转导途径,如G蛋白α亚基Gpa1、小GTP酶Ras1和非典型Gβ样/RACK1蛋白Gib2,在新型隐球菌的毒力中发挥重要作用。Gib2对正常生长、分化和致病性很重要,并且它还与Gpa1一起正向调节cAMP水平。有趣的是,Gib2通过与多种细胞蛋白相互作用而表现出支架蛋白特性。为了探索Gib2的全局调节功能,我们进行了二维差异凝胶电泳(DIGE)分析,发现GIB2缺失导致304个蛋白点(43.4%)的表达增加和396个蛋白点(56.6%)的表达减少。对96个表达变化被认为显著(≥+/- 1.5倍)的蛋白质进行分析发现,75个蛋白质属于至少12个功能蛋白组。其中,8个组具有p≤0.05的统计学显著性,包括Hsp70/71热休克蛋白同源物和核糖体蛋白在内的4个组在Bonferroni校正后仍具有统计学意义。这一发现与人类Gβ样/RACK1和芽殖酵母酿酒酵母Asc1早期确立的作用一致。这表明Gib2也可能是影响新型隐球菌核糖体生物合成和蛋白质翻译的复合物的一部分。由于真核生物Hsp70/71蛋白参与促进新生蛋白质折叠、加工以及保护细胞免受应激,我们还提出Gib2调节的应激反应与真菌毒力有关。总的来说,我们的研究支持Gβ样/RACK/Gib2蛋白在核糖体生物合成和蛋白质翻译这一基本细胞过程中的保守作用。我们的研究还突出了Gib2在新型隐球菌生长和致病性中的多方面调节作用。