Qiao Sha, Bernasek Sebastian, Gallagher Kevin D, Yamada Shigehiro, Bagheri Neda, Amaral Luis A N, Carthew Richard W
Department of Molecular Biosciences, Northwestern University, Evanston, IL.
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL.
bioRxiv. 2023 Oct 26:2023.10.24.563842. doi: 10.1101/2023.10.24.563842.
Gene expression is a regulated process fueled by ATP consumption. Therefore, regulation must be coupled to constraints imposed by the level of energy metabolism. Here, we explore this relationship both theoretically and experimentally. A stylized mathematical model predicts that activators of gene expression have variable impact depending on metabolic rate. Activators become less essential when metabolic rate is reduced and more essential when metabolic rate is enhanced. We find that in the eye, expression dynamics of the gene are less affected by loss of EGFR-mediated activation when metabolism is reduced, and the opposite effect is seen when metabolism is enhanced. The effects are also seen at the level of pattern regularity in the adult eye, where loss of EGFR-mediated activation is mitigated by lower metabolism. We propose that gene activation is tuned by energy metabolism to allow for faithful expression dynamics in the face of variable metabolic conditions.
基因表达是一个由ATP消耗驱动的受调控过程。因此,调控必须与能量代谢水平所施加的限制相耦合。在这里,我们从理论和实验两方面探索这种关系。一个程式化的数学模型预测,基因表达的激活剂根据代谢率具有可变的影响。当代谢率降低时,激活剂变得不那么重要,而当代谢率提高时,激活剂变得更加重要。我们发现在眼睛中,当代谢降低时,基因的表达动态受表皮生长因子受体(EGFR)介导的激活缺失的影响较小,而当代谢增强时则会出现相反的效果。在成年眼睛的模式规律性水平上也观察到了这些效应,其中较低的代谢减轻了EGFR介导的激活缺失。我们提出,基因激活由能量代谢进行调节,以便在面对可变的代谢条件时实现可靠的表达动态。