Abstract
Multistability is a crucial recurring theme in cell signaling. Multistability is attributed to the presence of positive feedback loops, but the general condition and essential mechanism for realizing multistability remain unclear. Here, we build a generic circuit model comprising two transcription factors and a microRNA, representing a kind of core architecture in gene regulatory networks. The circuit can be decomposed into two positive feedback loops (PFLs) or one PFL and one negative feedback loop (NFL), which are multiplicatively coupled. Bifurcation analyses of the model reveal that the circuit can achieve tristability through four kinds of bifurcation scenarios when parameter values are varied in a wide range. We formulate the general requirement for tristability in terms of logarithmic gain of the circuit. The parameter ranges for tristability and possible transition routes among steady states are determined by the combination of gain features of individual feedback loops. Coupling two PFLs with bistability or one NFL with a bistable PFL is most likely to generate tristability, but the underlying mechanisms are largely different. We also interpret published results and make testable predictions. This work sheds new light on interlinking feedback loops to realize tristability. The proposed theoretical framework can be of wide applicability.