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RetroSignalModel.jl

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rtgM4 model

Mitochondrial Retrograde Signalling

Mitochondrial retrograde signaling reports mitochondrial status to the nucleus. However, there is a lack of understanding of how the nucleus capture mitochondrial status in dynamics and information processing. It is a complicated biochemical reaction that occurs in most eukaryotic organisms. In this repository, we focus on the RTG pathway in yeast. This pathway is the simplest retrograde signaling pathway that has been investigated thoroughly. Data are collected from [1] and [2] (See Dataset). This repository aims to compose known protein interactions and nucleus relocation that fulfills all known responses of the yeast RTG pathway. Monte-Carlo approach is used to solve this Boolean satisfiability problem, and the parameter searching/ simulation/ threading is facilitated by DifferentialEquations.jl [3].

Installation

This repository is a Julia package. To use this function, one needs to install Julia v1.7+ first (https://julialang.org/).

Use the following script to install this package in Julia REPL.

using Pkg
Pkg.add(PackageSpec(url="https://github.com/ntumitolab/RetroSignalModel.jl"))

Implementation details

https://ntumitolab.github.io/RetroSignalModel.jl/dev/


RTG protein levels

https://github.com/ntumitolab/rnaseq_rtg_expression

Parameters of retrograde signaling model

Table of parameters: solution_rtgM4.csv

This file is generated and modified from a script. All solutions are corresponding to the knockout experiments of [1] and [2] with the conditions in boolean_table_RTG13.csv. The solutions are stored in solution_rtgM4.csv.

Responses of Yeast RTG proteins to mitochondrial damage

Data: boolean_table_RTG13.csv

This folder contains summarized responses of mitochondrial retrograde signaling in yeast.

Components

Standard Name Variable Name Details
RTG1 rtg1 https://www.yeastgenome.org/locus/S000005428
RTG2 rtg2 https://www.yeastgenome.org/locus/S000005428
RTG3 rtg3 https://www.yeastgenome.org/locus/S000000199
Mks1 mks1 https://www.yeastgenome.org/locus/S000005020

Definition of Response

In [1] and [2], RTG response is observed via GFP tags on either RTG1 or RTG3. In wild-type, mitochondrial damage can cause these proteins to accumulate in the nucleus, resulting in the intensified brightness of the nucleus region observed by fluorescent microscopy. As shown in boolean_table_RTG13.csv, the responses are categorized in binary results: whether GFP is accumulated in the nucleus in a given condition. Based on [1] and [2], there are 20 reactions listed in the table.

For example, the following is one of the conditions mentioned in [1]:

Rtg1 Rtg2 Rtg3 s Mks gfp Trans2Nuc
0 0 1 1 1 rtg3 1

Under the columns of Rtg1, Rtg2, Rtg3 and Mks, 0 means that the given protein is suppressed by knockout. On the other hand, 1 represent an expression of wild type. Also, 1 in s represent mitochondrial dysfunction, and 0 means the absence of mitochondrial damage. The gfp column describes the location of GFP tag. In this example, GFP tag is on Rtg3. As known in [1], Rtg3-GFP translocates to the nucleus under this condition. Therefore, Trans2Nuc is marked as 1, which means the GFP tags nucleus translocation happens.

Reactions

There are 20 reactions summarized in the table. Some conditions are yet to be explored; some are from [1] (Sekito et al. 2000) or [2] (Sekito et al. 2002). Missing conditions are labeled with NA.

Line Number Reference
2 NA
3 [1]
4 [1]
5 [1]
6 [1]
7 [1]
8 [1]
9 [1]
10 NA
11 NA
12 [1]
13 [1]
14 [1]
15 [1]
16 [1]
17 [1]
18 [2]
19 [2]
20 [2]
21 [2]

References

  1. Sekito, Takayuki, Janet Thornton, and Ronald A. Butow. "Mitochondria-to-nuclear signaling is regulated by the subcellular localization of the transcription factors Rtg1p and Rtg3p." Molecular biology of the cell 11.6 (2000): 2103-2115. URL: https://doi.org/10.1091/mbc.11.6.2103
  2. Sekito, Takayuki, Zhengchang Liu, Janet Thornton, and Ronald A. Butow. “RTG-Dependent Mitochondria-to-Nucleus Signaling Is Regulated by MKS1 and Is Linked to Formation of Yeast Prion [URE3].” Molecular Biology of the Cell 13, no. 3 (March 2002): 795–804. https://doi.org/10.1091/mbc.01-09-0473.
  3. Rackauckas, Christopher, and Qing Nie. “DifferentialEquations.Jl – A Performant and Feature-Rich Ecosystem for Solving Differential Equations in Julia.” Journal of Open Research Software 5, no. 1 (May 25, 2017): 15. https://doi.org/10.5334/jors.151.
  4. Gasch, Audrey P., et al. "Single-cell RNA sequencing reveals intrinsic and extrinsic regulatory heterogeneity in yeast responding to stress." PLoS biology 15.12 (2017): e2004050. URL: https://doi.org/10.1371/journal.pbio.2004050
  5. Delmans, Mihails, and Martin Hemberg. "Discrete distributional differential expression (D3E)-a tool for gene expression analysis of single-cell RNA-seq data." BMC bioinformatics 17.1 (2016): 1-13. URL: https://doi.org/10.1186/s12859-016-0944-6