Evidence map›Paper›PMID 25657653›Full record

ArticleFrontiers in plant science2015

A multi-tissue genome-scale metabolic modeling framework for the analysis of whole plant systems.

Cristiana Gomes de Oliveira Dal'Molin, Lake-Ee Quek, Pedro A Saa, Lars K Nielsen

Abstract read
In one paragraph

Article in Frontiers in plant science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

62 citing papers in PubMed.

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  19. Exploring synergies between plant metabolic modelling and machine learning.Computational and structural biotechnology journal · 2022
    Review
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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Cristiana Gomes de Oliveira Dal'MolinCentre for Systems and Synthetic Biology, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland Brisbane, Qld, Australia.
Lake-Ee QuekCentre for Systems and Synthetic Biology, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland Brisbane, Qld, Australia.
Pedro A SaaCentre for Systems and Synthetic Biology, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland Brisbane, Qld, Australia.
Lars K NielsenCentre for Systems and Synthetic Biology, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland Brisbane, Qld, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome scale metabolic modeling has traditionally been used to explore metabolism of individual cells or tissues. In higher organisms, the metabolism of individual tissues and organs is coordinated for the overall growth and well-being of the organism. Understanding the dependencies and rationale for multicellular metabolism is far from trivial. Here, we have advanced the use of AraGEM (a genome-scale reconstruction of Arabidopsis metabolism) in a multi-tissue context to understand how plants grow utilizing their leaf, stem and root systems across the day-night (diurnal) cycle. Six tissue compartments were created, each with their own distinct set of metabolic capabilities, and hence a reliance on other compartments for support. We used the multi-tissue framework to explore differences in the "division-of-labor" between the sources and sink tissues in response to: (a) the energy demand for the translocation of C and N species in between tissues; and (b) the use of two distinct nitrogen sources (NO(-) 3 or NH(+) 4). The "division-of-labor" between compartments was investigated using a minimum energy (photon) objective function. Random sampling of the solution space was used to explore the flux distributions under different scenarios as well as to identify highly coupled reaction sets in different tissues and organelles. Efficient identification of these sets was achieved by casting this problem as a maximum clique enumeration problem. The framework also enabled assessing the impact of energetic constraints in resource (redox and ATP) allocation between leaf, stem, and root tissues required for efficient carbon and nitrogen assimilation, including the diurnal cycle constraint forcing the plant to set aside resources during the day and defer metabolic processes that are more efficiently performed at night. This study is a first step toward autonomous modeling of whole plant metabolism.

Indexed as

AraGEMgenome-scalemodelingmulti-tissueplant metabolism

Identifiers

PMID25657653
PMCPMC4302846

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.