# Evaluating transcriptomic integration for cyanobacterial constraint-based metabolic modelling

**Authors:** Thomas Pugsley, Guy Hanke, Christopher D. P. Duffy

PMC · DOI: 10.3389/fbinf.2026.1715377 · Frontiers in Bioinformatics · 2026-02-04

## TL;DR

This paper evaluates methods for integrating transcriptomic data into metabolic models of cyanobacteria to better predict cellular processes.

## Contribution

The study provides a systematic evaluation of transcriptomic integration methods for cyanobacterial metabolic modeling.

## Key findings

- METRADE* with single objective optimization performs best for predicting fluxes in cyanobacteria.
- Configuration and scaling are critical for achieving accurate metabolic model predictions.
- Few validation studies exist for cyanobacteria due to limited flux data availability.

## Abstract

Metabolic modelling has wide-ranging applications, including for the improved production of high-value compounds, understanding complex diseases and analysing microbial community interactions. Integrating transcriptomic data with genome-scale metabolic models is crucial for deepening our understanding of complex biological systems, as it enables the development of models tailored to specific conditions, such as particular tissues, environments, or experimental setups. Relatively little attention has been given to the validation and comparison of such integration methods in predicting intracellular fluxes. While a few validation studies offer some insights, their scope remains limited, particularly for organisms like cyanobacteria, for which little metabolic flux data are available. Cyanobacteria hold significant biotechnological potential due to their ability to synthesise a wide range of high-value compounds with minimal resource inputs. Using existing transcriptomic data, we evaluated different methodological options that can be taken when integrating transcriptomics with a genome-scale metabolic model of Synechocystis sp. PCC 6803 (iSynCJ816), when predicting autotrophic flux distributions. We find METRADE* (using single objective optimisation) to be the best-performing method in cyanobacteria owing to its ability to perform well across both metrics but emphasise the importance of configuration and scaling in achieving these outcomes.

## Linked entities

- **Species:** Synechocystis sp. PCC 6803 (taxon 1148)

## Full-text entities

- **Diseases:** renal cancer (MESH:D007680), cancer (MESH:D009369)
- **Chemicals:** glucose (MESH:D005947), bicarbonate (MESH:D001639), carbohydrate (MESH:D002241), 13C-MFA (-), 13C (MESH:C000615229), E (MESH:D004540), water (MESH:D014867), nitrogen (MESH:D009584), carbon (MESH:D002244), mycolic acid (MESH:D009171), oxygen (MESH:D010100)
- **Species:** Synechococcus sp. (species) [taxon 1131], Synechocystis sp. (species) [taxon 1143], Homo sapiens (human, species) [taxon 9606], Cyanobacteriota (blue-green algae, phylum) [taxon 1117], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** PCC 6803 — Homo sapiens (Human), Transformed cell line (CVCL_A6SD), CHO — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0213)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913417/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913417/full.md

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Source: https://tomesphere.com/paper/PMC12913417