Hodgens Charles, Flaherty D T, Pullen Anne-Marie, Khan Imran, English Nolan J, Gillan Lydia, Rojas-Pierce Marcela, Akpa Belinda S
Department of Chemical and Biomolecular Engineering, University of Tennessee-Knoxville, Knoxville, Tennessee, USA.
Department of Molecular Biomedical Sciences, North Carolina State University, Raleigh, North Carolina, USA.
bioRxiv. 2023 Nov 9:2023.11.07.565947. doi: 10.1101/2023.11.07.565947.
Stomata are the pores on a leaf surface that regulate gas exchange. Each stoma consists of two guard cells whose movements regulate pore opening and thereby control CO fixation and water loss. Guard cell movements depend in part on the remodeling of vacuoles, which have been observed to change from a highly fragmented state to a fused morphology during stomata opening. This change in morphology requires a membrane fusion mechanism that responds rapidly to environmental signals, allowing plants to respond to diurnal and stress cues. With guard cell vacuoles being both large and responsive to external signals, stomata represent a unique system in which to delineate mechanisms of membrane fusion. Fusion of vacuole membranes is a highly conserved process in eukaryotes, with key roles played by two multi-subunit complexes: HOPS (homotypic fusion and vacuolar protein sorting) and SNARE (soluble NSF attachment protein receptor). HOPS is a vacuole tethering factor that is thought to chaperone SNAREs from apposing vacuole membranes into a fusion-competent complex capable of rearranging membranes. To resolve a counter-intuitive observation regarding the role of HOPS in regulating plant vacuole morphology, we derived a quantitative model of vacuole fusion dynamics and used it to generate testable predictions about HOPS-SNARE interactions. We derived our model by applying simulation-based inference to integrate prior knowledge about molecular interactions with limited, qualitative observations of emergent vacuole phenotypes. By constraining the model parameters to yield the emergent outcomes observed for stoma opening - as induced by two distinct chemical treatments - we predicted a dual role for HOPS and identified a stalled form of the SNARE complex that differs from phenomena reported in yeast. We predict that HOPS has contradictory actions at different points in the fusion signaling pathway, promoting the formation of SNARE complexes, but limiting their activity.
气孔是叶片表面调节气体交换的孔隙。每个气孔由两个保卫细胞组成,保卫细胞的运动调节气孔的开闭,从而控制二氧化碳固定和水分流失。保卫细胞的运动部分取决于液泡的重塑,在气孔开放过程中,液泡已被观察到从高度碎片化状态转变为融合形态。这种形态变化需要一种能对环境信号快速做出反应的膜融合机制,使植物能够对昼夜和胁迫信号做出反应。由于保卫细胞液泡既大又能对外部信号做出反应,气孔代表了一个独特的系统,可用于描绘膜融合机制。液泡膜融合在真核生物中是一个高度保守的过程,由两个多亚基复合物发挥关键作用:同型融合和液泡蛋白分选(HOPS)复合物以及可溶性N-乙基马来酰胺敏感因子附着蛋白受体(SNARE)复合物。HOPS是一种液泡拴系因子,被认为能将来自相对液泡膜的SNARE分子伴侣成一个能够重排膜的有融合能力的复合物。为了解决关于HOPS在调节植物液泡形态中的作用这一违反直觉的观察结果,我们推导了一个液泡融合动力学的定量模型,并利用它来生成关于HOPS-SNARE相互作用的可测试预测。我们通过应用基于模拟的推理来推导模型,将关于分子相互作用的先验知识与对出现的液泡表型的有限定性观察相结合。通过约束模型参数以产生由两种不同化学处理诱导的气孔开放所观察到的出现结果,我们预测了HOPS的双重作用,并确定了一种与酵母中报道的现象不同的SNARE复合物停滞形式。我们预测HOPS在融合信号通路的不同点具有相互矛盾的作用,促进SNARE复合物的形成,但限制其活性。