Systems analysis of miR-199a/b-5p and multiple miR-199a/b-5p targets during chondrogenesis

Changes in chondrocyte gene expression can contribute to the development of osteoarthritis (OA), and so recognition of the regulative processes during chondrogenesis can lead to a better understanding of OA. microRNAs (miRNAs) are key regulators of gene expression in chondrocytes/OA, and we have used a combined experimental, bioinformatic, and systems biology approach to explore the multiple miRNA–mRNA interactions that regulate chondrogenesis. A longitudinal chondrogenesis bioinformatic analysis identified paralogues miR-199a-5p and miR-199b-5p as pro-chondrogenic regulators. Experimental work in human cells demonstrated alteration of miR-199a-5p or miR-199b-5p expression led to significant inverse modulation of key chondrogenic genes and extracellular matrix production. miR-199a/b-5p targets FZD6, ITGA3 and CAV1 were identified by inhibition experiments and verified as direct targets by luciferase assay. The experimental work was used to generate and parameterise a multi-miRNA 14-day chondrogenesis kinetic model to be used as a repository for the experimental work and as a resource for further investigation of this system. This is the first multi-miRNA model of a chondrogenesis-based system, and highlights the complex relationships between regulatory miRNAs, and their target mRNAs.

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Publication Details

Journal
eLife
Published
2024-10-14
DOI
https://doi.org/10.7554/elife.89701.4
Citations
2
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
Field-Weighted Citation Impact
0.94

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article

Systems analysis of miR-199a/b-5p and multiple miR-199a/b-5p targets during chondrogenesis

Carole J. Proctor, David A. Young, Daryl P. Shanley, Krutik Patel et al.
2 citations
eLife
Osteoarthritis Treatment and Mechanisms
0.94
article

Systems analysis of miR-199a/b-5p and multiple miR-199a/b-5p targets during chondrogenesis

Carole J. Proctor, David A. Young, Daryl P. Shanley, Krutik Patel, Jamie Soul, Matt J. Barter, Peter A. Clark, Ian M. Clark
article en
2 citations

Abstract

Changes in chondrocyte gene expression can contribute to the development of osteoarthritis (OA), and so recognition of the regulative processes during chondrogenesis can lead to a better understanding of OA. microRNAs (miRNAs) are key regulators of gene expression in chondrocytes/OA, and we have used a combined experimental, bioinformatic, and systems biology approach to explore the multiple miRNA–mRNA interactions that regulate chondrogenesis. A longitudinal chondrogenesis bioinformatic analysis identified paralogues miR-199a-5p and miR-199b-5p as pro-chondrogenic regulators. Experimental work in human cells demonstrated alteration of miR-199a-5p or miR-199b-5p expression led to significant inverse modulation of key chondrogenic genes and extracellular matrix production. miR-199a/b-5p targets FZD6, ITGA3 and CAV1 were identified by inhibition experiments and verified as direct targets by luciferase assay. The experimental work was used to generate and parameterise a multi-miRNA 14-day chondrogenesis kinetic model to be used as a repository for the experimental work and as a resource for further investigation of this system. This is the first multi-miRNA model of a chondrogenesis-based system, and highlights the complex relationships between regulatory miRNAs, and their target mRNAs.

eLifeVol. 12
University of East Anglia (GB), University of Liverpool (GB), Newcastle Hospitals - Campus for Ageing and Vitality (GB), Health & Life (Taiwan) (TW), University of Newcastle Australia (AU), Newcastle University (GB)
Dunhill Medical Trust, Novo Nordisk Fonden, Versus Arthritis
Openalex Percentile: Top 22%
Osteoarthritis Treatment and Mechanisms
0.94
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