Abstract

It is well known that gene regulation is a tightly controlled process in early organismal development. However, the roles of key processes involved in this regulation, such as transcription and translation, are less well understood, and mathematical modeling approaches in this field are still in their infancy. In recent studies, biologists have taken precise measurements of protein and mRNA abundance to determine the relative contributions of key factors involved in regulating protein levels in mammalian cells. We now approach this question from a mathematical modeling perspective. In this study, we use a simple dynamic mathematical model that incorporates terms representing transcription, translation, mRNA and protein decay, and diffusion in an early Drosophila embryo. We perform global sensitivity analyses on this model using various different initial conditions and spatial and temporal outputs. Our results indicate that transcription and translation are often the key parameters to determine protein abundance. This observation is in close agreement with the experimental results from mammalian cells for various initial conditions at particular time points, suggesting that a simple dynamic model can capture the qualitative behavior of a gene. Additionally, we find that parameter sensitivites are temporally dynamic, illustrating the importance of conducting a thorough global sensitivity analysis across multiple time points when analyzing mathematical models of gene regulation.

Highlights

  • Gene regulation in embryonic development Embryonic development in animals is very precisely controlled by a network of regulatory proteins (Davidson, 2010; Peter and Davidson, 2011)

  • Transcription is the process of reading a gene in a DNA template to produce a messenger RNA, while translation is the process of reading the mRNA to produce a protein

  • We have used parameter sensitivity analysis to try to unravel the importance of parameter values in a reaction–diffusion model and in doing so to better understand the power of this modeling approach as well as the relative contribution of transcription and translation in regulating protein abundance

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Summary

INTRODUCTION

Gene regulation in embryonic development Embryonic development in animals is very precisely controlled by a network of regulatory proteins (Davidson, 2010; Peter and Davidson, 2011). We utilize a global HDMR analysis to investigate the sensitivity of our Drosophila embryo gene expression model to the individual transcription, translation, diffusion, and decay rate parameters and higher-order interactions between these parameters. We compare our results to those in mammalian cells and other studies that have attempted to model different gene expression systems (Li, Bickel & Biggin, 2014)

METHODS
Objective function
Findings
DISCUSSION

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