Cytoplasmic polyadenylation by TENT5A is required for proper bone formation
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
33882302
DOI
10.1016/j.celrep.2021.109015
PII: S2211-1247(21)00329-6
Knihovny.cz E-resources
- Keywords
- FAM46A, Nanopore, TENT5A, collagen, direct RNA sequencing, osteoblasts, osteogenesis, osteogenesis imperfecta, poly(A) tail, polyadenylation,
- MeSH
- Cell Differentiation MeSH
- Calcification, Physiologic genetics MeSH
- Collagen Type I, alpha 1 Chain genetics metabolism MeSH
- Collagen Type I genetics metabolism MeSH
- Humans MeSH
- RNA, Messenger genetics metabolism MeSH
- Disease Models, Animal MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Nerve Growth Factors genetics metabolism MeSH
- Nucleotidyltransferases genetics metabolism MeSH
- Eye Proteins genetics metabolism MeSH
- Osteoblasts metabolism pathology MeSH
- Osteogenesis Imperfecta genetics metabolism pathology MeSH
- Osteogenesis genetics MeSH
- Osteonectin genetics metabolism MeSH
- Polynucleotide Adenylyltransferase genetics metabolism MeSH
- Polyadenylation MeSH
- Protein Isoforms deficiency genetics MeSH
- Sequence Analysis, RNA MeSH
- Serpins genetics metabolism MeSH
- Signal Transduction MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Col1a1 protein, mouse MeSH Browser
- Col1a2 protein, mouse MeSH Browser
- Collagen Type I, alpha 1 Chain MeSH
- Collagen Type I MeSH
- RNA, Messenger MeSH
- Nerve Growth Factors MeSH
- Nucleotidyltransferases MeSH
- Eye Proteins MeSH
- Osteonectin MeSH
- pigment epithelium-derived factor MeSH Browser
- Polynucleotide Adenylyltransferase MeSH
- Protein Isoforms MeSH
- Serpins MeSH
- SPARC protein, mouse MeSH Browser
- TENT5A protein, human MeSH Browser
- Tent5A protein, mouse MeSH Browser
- Tent5c protein, mouse MeSH Browser
Osteoblasts orchestrate bone formation through the secretion of type I collagen and other constituents of the matrix on which hydroxyapatite crystals mineralize. Here, we show that TENT5A, whose mutations were found in congenital bone disease osteogenesis imperfecta patients, is a cytoplasmic poly(A) polymerase playing a crucial role in regulating bone mineralization. Direct RNA sequencing revealed that TENT5A is induced during osteoblast differentiation and polyadenylates mRNAs encoding Col1α1, Col1α2, and other secreted proteins involved in osteogenesis, increasing their expression. We postulate that TENT5A, possibly together with its paralog TENT5C, is responsible for the wave of cytoplasmic polyadenylation of mRNAs encoding secreted proteins occurring during bone mineralization. Importantly, the Tent5a knockout (KO) mouse line displays bone fragility and skeletal hypomineralization phenotype resulting from quantitative and qualitative collagen defects. Thus, we report a biologically relevant posttranscriptional regulator of collagen production and, more generally, bone formation.
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