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Explore the dynamics of gene regulation in Mixed Feedback Loops (MFLs) using stochastic analysis, revealing bi-stability and meta-stability. Learn about the impact of sRNAs and protein-protein interactions in this integrated network study.
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Stochastic Analysis of Bi-stability in Mixed Feedback Loops Yishai Shimoni, Hebrew University CCS Open Day Sep 18th 2008
An Integrated Network • A feedback loop consists of two genes that regulate each other’s expression • In a Mixed Feedback Loop (MFL) each gene uses a different mechanism for the regulation
Small RNAs (sRNAs) • Non-coding RNA molecules • 50-400 nucleotides long • Base-pairs with mRNAs and influences translation (normally repression) • Approximately 100 sRNAs identified in E. coli • Participate mostly in stress responses due to fast synthesis
Double Negative Mixed Feedback Loop (MFL) A s B A Time (sec x 105) Time (sec x 104) Bi-stability Meta-stability
Double Negative MFL • Questions: • How much of the parameter range displays a meta-stable state? • Does this happen with protein-protein interactions as well? • What is the difference? • Run the Monte Carlo simulation with different parameters and check if the state (A dominated or s/B dominated) changes during a given time
Double Negative MFL Phase Map of bi-stability in sRNA double negative MFL
Double Negative MFL Phase Map of bi-stability in protein-protein double negative MFL
Double Negative MFL • Conclusion: • Stochastic analysis reveals a new dynamic behavior • Cannot be seen using deterministic analysis • Quantitative difference between MFLs with sRNA regulation and MFLs with protein-protein interaction • Both have same qualitative dynamics • Do simulations fit reality?
In the presence of iron Fur represses RyhB transcription Iron depletion: Fur does not repress RyhB RyhB highly expressed RyhB Regulates many iron uptake genes Fur-RyhB MFL in E. Coli
Fur-RyhB MFL in E. Coli • Bi-stability is unsuitable RyhB Fur Time (sec x 10-5) • A meta-stable state is perfect! RyhB Fur Time (sec x 10-4)
Summary • Post transcriptional regulation by sRNA • Offers different dynamics than other kinds of regulation • The dynamics are utilized by the cell • Mathematical Models using stochastic analysis can capture important features of the dynamics of biological networks
Acknowledgements • Modeling: • Prof. Ofer Biham • Adiel Loinger • Guy Hetzroni • Networks integration, circuit identification: • Prof. Hanah Margalit • Dr. Gilgi Friedlander • Gali Niv • Parameters and sRNA: • Prof. Shoshy Altuvia Y. Shimoni et. Al, submitted to PLoS Comp Biol