Parameterising Translational Feedback Models of Autoregulatory RNA-Binding Proteins in Saccharomyces cerevisiae
Michael Clarke-Whittet1,2, Andrea Rocco2,3, André P Gerber2
1Leverhulme Quantum Biology Doctoral Training Centre, University of Surrey, Guildford GU2 7XH, UK.
Abstract:
Post-transcriptional gene regulation is driven by RNA-binding proteins (RBPs). Recent global approaches suggest widespread autoregulation of RBPs through binding to their own mRNA; however, little is known about the regulatory impact and quantitative models remain elusive. By integration of several independent kinetic parameters and abundance data, we modelled autoregulatory feedback loops for six canonical and non-canonical RBPs from the yeast Saccharomyces cerevisiae, namely Hrb1p, Hek2/Khd1p, Ski2p, Npl3p, Pfk2p, and Map1p. By numerically solving ordinary differential equations, we compared non-feedback models with models that considered the RPBs as post-transcriptional activators/repressors of their own expression. While our results highlight a substantial gap between predicted protein output and experimentally determined protein abundances applying a no-feedback model, addition of positive feedback loops are surprisingly versatile and can improve predictions towards experimentally determined protein levels, whereas negative feedbacks are particularly sensitive to cooperativity. Our data suggests that introduction of feedback loops supported by real data can improve models of post-transcriptional gene expression.
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Types of RNA
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
RNA...


