Search bioRxiv⌕ Search

Biology subjects

Shojaosadati, S. A.

Publications and source records attributed to Shojaosadati, S. A..

2 recordsLinked to original sources

MRI: an algorithm to identify metabolic reprogramming during adaptive laboratory evolution using gene expression data

The development of a method for identifying latent reprogramming in gene expression data resulting from evolution has been a challenge. In this study, a method called Metabolic Reprogramming Identifier (MRI), based on the integration of expression data to a genome-scale metabolic model, has been developed. To identify key genes playing the main role in reprogramming, a MILP problem is presented and maximum utilization of gene expression resources is defined as an objective function. Then, genes with complete expression usage and significant expression difference between wild-type and evolved strains were selected as key genes for reprogramming. This score is also applied to evaluate compatibility of expression pattern with maximal use of key genes. The method was implemented to investigate the reprogramming of E. coli during adaptive evolution caused by changing carbon sources. The results indicate the importance of inner membrane in reprogramming of E. coli to adapt to the new environment. The method predicts no reprogramming occurs when switching from glucose to glycerol.

evolutionary biology↗

Reconstruction of a generic genome-scale metabolic network for chicken: investigating network connectivity and finding potential biomarkers

Chicken is the first sequenced avian that has a crucial role in human life for its meat and egg production. Because of various metabolic disorders, study the metabolism of chicken cell is important. Herein, the first genome-scale metabolic model of a chicken cell named iES1300, consists of 2427 reactions, 2569 metabolites, and 1300 genes, was reconstructed manually based on databases. Interactions of metabolic genes for growth were examined for E. coli, S. cerevisiae, human, and chicken metabolic models. The results indicated robustness to genetic manipulation for iES1300 similar to the results for human. iES1300 was integrated with transcriptomics data using algorithms and Principal Component Analysis was applied to compare context-specific models of the normal, tumor, lean and fat cell lines. It was found that the normal model has notable metabolic flexibility in the utilization of various metabolic pathways, especially in metabolic pathways of the carbohydrate metabolism, compared to the others. It was also concluded that the fat and tumor models have similar growth metabolisms and the lean chicken model has a more active lipid and carbohydrate metabolism.

systems biology↗