» Articles » PMID: 37093889

MultiCens: Multilayer Network Centrality Measures to Uncover Molecular Mediators of Tissue-tissue Communication

Overview
Specialty Biology
Date 2023 Apr 24
PMID 37093889
Authors
Affiliations
Soon will be listed here.
Abstract

With the evolution of multicellularity, communication among cells in different tissues and organs became pivotal to life. Molecular basis of such communication has long been studied, but genome-wide screens for genes and other biomolecules mediating tissue-tissue signaling are lacking. To systematically identify inter-tissue mediators, we present a novel computational approach MultiCens (Multilayer/Multi-tissue network Centrality measures). Unlike single-layer network methods, MultiCens can distinguish within- vs. across-layer connectivity to quantify the "influence" of any gene in a tissue on a query set of genes of interest in another tissue. MultiCens enjoys theoretical guarantees on convergence and decomposability, and performs well on synthetic benchmarks. On human multi-tissue datasets, MultiCens predicts known and novel genes linked to hormones. MultiCens further reveals shifts in gene network architecture among four brain regions in Alzheimer's disease. MultiCens-prioritized hypotheses from these two diverse applications, and potential future ones like "Multi-tissue-expanded Gene Ontology" analysis, can enable whole-body yet molecular-level systems investigations in humans.

Citing Articles

InTiCAR: Network-based identification of significant inter-tissue communicators for autoimmune diseases.

Kim K, Han M, Lee D Comput Struct Biotechnol J. 2025; 27:333-345.

PMID: 39897058 PMC: 11782887. DOI: 10.1016/j.csbj.2025.01.003.


A generalized eigenvector centrality for multilayer networks with inter-layer constraints on adjacent node importance.

Frost H Appl Netw Sci. 2024; 9(1):14.

PMID: 38699246 PMC: 11060970. DOI: 10.1007/s41109-024-00620-8.


Leveraging inter-individual transcriptional correlation structure to infer discrete signaling mechanisms across metabolic tissues.

Zhou M, Tamburini I, Van C, Molendijk J, Nguyen C, Chang I Elife. 2024; 12.

PMID: 38224289 PMC: 10945578. DOI: 10.7554/eLife.88863.


An Exploratory Application of Multilayer Networks and Pathway Analysis in Pharmacogenomics.

Milano M, Agapito G, Cannataro M Genes (Basel). 2023; 14(10).

PMID: 37895264 PMC: 10606656. DOI: 10.3390/genes14101915.

References
1.
Droujinine I, Meyer A, Wang D, Udeshi N, Hu Y, Rocco D . Proteomics of protein trafficking by in vivo tissue-specific labeling. Nat Commun. 2021; 12(1):2382. PMC: 8062696. DOI: 10.1038/s41467-021-22599-x. View

2.
McKenzie A, Wang M, Hauberg M, Fullard J, Kozlenkov A, Keenan A . Brain Cell Type Specific Gene Expression and Co-expression Network Architectures. Sci Rep. 2018; 8(1):8868. PMC: 5995803. DOI: 10.1038/s41598-018-27293-5. View

3.
Kefi S, Miele V, Wieters E, Navarrete S, Berlow E . How Structured Is the Entangled Bank? The Surprisingly Simple Organization of Multiplex Ecological Networks Leads to Increased Persistence and Resilience. PLoS Biol. 2016; 14(8):e1002527. PMC: 4972357. DOI: 10.1371/journal.pbio.1002527. View

4.
Droujinine I, Perrimon N . Defining the interorgan communication network: systemic coordination of organismal cellular processes under homeostasis and localized stress. Front Cell Infect Microbiol. 2013; 3:82. PMC: 3832798. DOI: 10.3389/fcimb.2013.00082. View

5.
Seldin M, Koplev S, Rajbhandari P, Vergnes L, Rosenberg G, Meng Y . A Strategy for Discovery of Endocrine Interactions with Application to Whole-Body Metabolism. Cell Metab. 2018; 27(5):1138-1155.e6. PMC: 5935137. DOI: 10.1016/j.cmet.2018.03.015. View