4.7 Review

Reviewing the Regulators of COL1A1

Journal

Publisher

MDPI
DOI: 10.3390/ijms241210004

Keywords

collagen; collagen type I alpha 1 chain; molecular signalling pathways; disease

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The collagen family consists of 28 proteins, mainly expressed in the extracellular matrix (ECM) and characterized by a triple-helix structure. Collagens undergo various maturation steps, including post-translational modifications (PTMs) and cross-linking. These proteins are associated with several diseases, with fibrosis and bone diseases being the most prominent. This review focuses on type I collagen (collagen I), the most abundant ECM protein highly implicated in disease, particularly on its predominant chain collagen type I alpha 1 (COL1A1). The regulators and interactors of COL1A1 are discussed, highlighting the need for a comprehensive analysis considering all molecular levels simultaneously.
The collagen family contains 28 proteins, predominantly expressed in the extracellular matrix (ECM) and characterized by a triple-helix structure. Collagens undergo several maturation steps, including post-translational modifications (PTMs) and cross-linking. These proteins are associated with multiple diseases, the most pronounced of which are fibrosis and bone diseases. This review focuses on the most abundant ECM protein highly implicated in disease, type I collagen (collagen I), in particular on its predominant chain collagen type I alpha 1 (COL & alpha;1 (I)). An overview of the regulators of COL & alpha;1 (I) and COL & alpha;1 (I) interactors is presented. Manuscripts were retrieved searching PubMed, using specific keywords related to COL & alpha;1 (I). COL1A1 regulators at the epigenetic, transcriptional, post-transcriptional and post-translational levels include DNA Methyl Transferases (DNMTs), Tumour Growth Factor & beta; (TGF & beta;), Terminal Nucleotidyltransferase 5A (TENT5A) and Bone Morphogenic Protein 1 (BMP1), respectively. COL & alpha;1 (I) interacts with a variety of cell receptors including integrin & beta;, Endo180 and Discoidin Domain Receptors (DDRs). Collectively, even though multiple factors have been identified in association to COL & alpha;1 (I) function, the implicated pathways frequently remain unclear, underscoring the need for a more spherical analysis considering all molecular levels simultaneously.

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