West Christopher M, van der Wel Hanke, Wang Zhuo A
Department of Biochemistry and Molecular Biology and the Oklahoma Center for Medical Glycobiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104 USA.
Development. 2007 Sep;134(18):3349-58. doi: 10.1242/dev.000893. Epub 2007 Aug 15.
Development in multicellular organisms is subject to both environmental and internal signals. In Dictyostelium, starvation induces amoebae to form migratory slugs that translocate from subterranean areas to exposed sites, where they culminate to form sessile fruiting bodies. Culmination, thought to be regulated by anterior tip cells, is selectively suppressed by mild hypoxia by a mechanism that can be partially overridden by another environmental signal, overhead light, or genetic activation of protein kinase A. Dictyostelium expresses, in all cells, an O2-dependent prolyl 4-hydroxylase (P4H1) required for O-glycosylation of Skp1, a subunit of E3SCF-Ub-ligases. P4H1-null cells differentiate the basic pre-stalk and pre-spore cell types but exhibit a selectively increased O2 requirement for culmination, from approximately 12% to near or above ambient (21%) levels. Overexpression of P4H1 reduces the O2 requirement to <5%. The requirement for P4H1 can be met by forced expression of the active enzyme in either pre-stalk (anterior) or pre-spore (posterior) cells, or replaced by protein kinase A activation or addition of small numbers of wild-type cells. P4H1-expressing cells accumulate at the anterior end, suggesting that P4H1 enables transcellular signaling by the tip. The evidence provides novel genetic support for the animal-derived O2-sensor model of prolyl 4-hydroxylase function, in an organism that lacks the canonical HIFalpha transcriptional factor subunit substrate target that is a feature of animal hypoxic signaling.
多细胞生物的发育受到环境和内部信号的双重影响。在盘基网柄菌中,饥饿会诱导变形虫形成迁移性蛞蝓,这些蛞蝓从地下区域转移到暴露的地点,并在那里发育形成固定的子实体。发育过程被认为受前端细胞调控,轻度缺氧会选择性地抑制这一过程,其机制可被另一种环境信号(头顶光)或蛋白激酶A的基因激活部分克服。盘基网柄菌在所有细胞中都表达一种O2依赖性脯氨酰4-羟化酶(P4H1),它是E3SCF-Ub连接酶亚基Skp1的O-糖基化所必需的。P4H1基因缺失的细胞能分化出基本的前柄细胞和前孢子细胞类型,但在发育过程中对O2的需求选择性增加,从大约12%升至接近或高于环境水平(21%)。P4H1的过表达将O2需求降低至<5%。在柄细胞(前端)或孢子细胞(后端)中强制表达活性酶可满足对P4H1的需求,或者通过蛋白激酶A激活或添加少量野生型细胞来替代。表达P4H1的细胞在前端聚集,这表明P4H1能够使前端进行跨细胞信号传导。这一证据为脯氨酰4-羟化酶功能的动物源O2传感器模型提供了新的遗传学支持,该模型存在于一个缺乏动物缺氧信号特征性的典型HIFα转录因子亚基底物靶点的生物体中。