Evidence map›Paper›PMID 31856706›Full record

ArticleBMC molecular and cell biology2019

Data-driven multiscale modeling reveals the role of metabolic coupling for the spatio-temporal growth dynamics of yeast colonies.

Jukka Intosalmi, Adrian C Scott, Michelle Hays, Nicholas Flann, Olli Yli-Harja, Harri Lähdesmäki, Aimée M Dudley, Alexander Skupin

Abstract read
In one paragraph

Article in BMC molecular and cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Jukka IntosalmiDepartment of Computer Science, Aalto University, P.O.Box 15400, Aalto, FI-00076, Finland. jukka.intosalmi@gmail.com.
Adrian C ScottPacific Northwest Research Institute, 720 Broadway, Seattle, WA, 98122, USA.
Michelle HaysMolecular and Cellular Biology Program, University of Washington, Seattle, WA, 98195, USA.
Nicholas FlannDepartment of Computer Science, Utah State University, 4205 Old Main Hill, Logan, UT, 84322, USA.
Olli Yli-HarjaBioMediTech and Faculty of Biomedical Sciences and Engineering, Tampere University of Technology, P.O.Box 553, Tampere, 33101, Finland.
Harri LähdesmäkiDepartment of Computer Science, Aalto University, P.O.Box 15400, Aalto, FI-00076, Finland.
Aimée M DudleyPacific Northwest Research Institute, 720 Broadway, Seattle, WA, 98122, USA.
Alexander SkupinLuxembourg Centre for Systems Biomedicine, University of Luxembourg, 2, avenue de l'Université, Esch-sur-Alzette, L-4365, Luxembourg. alexander.skupin@uni.lu.ORCID http://orcid.org/0000-0002-8955-8304

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI DUDLEY, AIMEE M · 2006 to 2016
$30.6M
NIGMS NIH HHS P50 GM076547
6 · The paper itself

Abstract

backgroundMulticellular entities like mammalian tissues or microbial biofilms typically exhibit complex spatial arrangements that are adapted to their specific functions or environments. These structures result from intercellular signaling as well as from the interaction with the environment that allow cells of the same genotype to differentiate into well-organized communities of diversified cells. Despite its importance, our understanding how this cell-cell and metabolic coupling lead to functionally optimized structures is still limited.

resultsHere, we present a data-driven spatial framework to computationally investigate the development of yeast colonies as such a multicellular structure in dependence on metabolic capacity. For this purpose, we first developed and parameterized a dynamic cell state and growth model for yeast based on on experimental data from homogeneous liquid media conditions. The inferred model is subsequently used in a spatially coarse-grained model for colony development to investigate the effect of metabolic coupling by calibrating spatial parameters from experimental time-course data of colony growth using state-of-the-art statistical techniques for model uncertainty and parameter estimations. The model is finally validated by independent experimental data of an alternative yeast strain with distinct metabolic characteristics and illustrates the impact of metabolic coupling for structure formation.

conclusionsWe introduce a novel model for yeast colony formation, present a statistical methodology for model calibration in a data-driven manner, and demonstrate how the established model can be used to generate predictions across scales by validation against independent measurements of genetically distinct yeast strains.

Indexed as

Computer SimulationModels, BiologicalSaccharomyces cerevisiaeSpatio-Temporal AnalysisBayesian optimizationDiauxic shiftMarkov chain Monte CarloMetabolic couplingMulticellular systemsMultiscale modelingYeast colony

Identifiers

PMID31856706
PMCPMC6923950

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.