Abstract

The molecular regulatory network (MRN) within a cell determines cellular states and transitions between them. Thus, modeling of MRNs is crucial, but this usually requires extensive analysis of time-series measurements, which is extremely difficult to obtain from biological experiments. However, single-cell measurement data such as single-cell RNA-sequencing databases have recently provided a new insight into resolving this problem by ordering thousands of cells in pseudo-time according to their differential gene expressions. Neural network modeling can be employed by using temporal data as learning data. In contrast, Boolean network modeling of MRNs has a growing interest, as it is a parameter-free logical modeling and thereby robust to noisy data while still capturing essential dynamics of biological networks. In this study, we propose a Boolean feedforward neural network (FFN) modeling by combining neural network and Boolean network modeling approach to reconstruct a practical and useful MRN model from large temporal data. Furthermore, analyzing the reconstructed MRN model can enable us to identify control targets for potential cellular state conversion. Here, we show the usefulness of Boolean FFN modeling by demonstrating its applicability through a toy model and biological networks.

Highlights

  • Cellular behavior is governed by intracellular molecular regulatory networks (MRNs), such as signaling and gene regulatory networks (Schmidt et al, 2005; Kim and Cho, 2006; Sreenath et al, 2008; Kim et al, 2011)

  • The eventual goal of our study is to identify control targets that can induce desired cellular state conversion, and for this purpose, we propose to build cell fate transition FFN (cFFN) using iFFN, tFFN, and fFFN based on temporal data measurements of network nodes

  • One most important application of such data is developing a mathematical model of the MRN within a cell since it determines cellular dynamic behaviors

Read more

Summary

Introduction

Cellular behavior is governed by intracellular molecular regulatory networks (MRNs), such as signaling and gene regulatory networks (Schmidt et al, 2005; Kim and Cho, 2006; Sreenath et al, 2008; Kim et al, 2011). Single-cell RNA sequencing technologies can measure messenger RNA concentration of hundreds to thousands of genes expressed by single cells, and single cell proteomics by mass spectrometry can quantify over 1,000 proteins per single cell at once (Budnik et al, 2018; Lun and Bodenmiller, 2020).

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call