Noncoding RNAs in skeletal development and disorders.
Qing YaoTailin HeJian-You LiaoRongdong LiaoXiaohao WuLijun LinGuozhi XiaoPublished in: Biological research (2024)
Protein-encoding genes only constitute less than 2% of total human genomic sequences, and 98% of genetic information was previously referred to as "junk DNA". Meanwhile, non-coding RNAs (ncRNAs) consist of approximately 60% of the transcriptional output of human cells. Thousands of ncRNAs have been identified in recent decades, and their essential roles in the regulation of gene expression in diverse cellular pathways associated with fundamental cell processes, including proliferation, differentiation, apoptosis, and metabolism, have been extensively investigated. Furthermore, the gene regulation networks they form modulate gene expression in normal development and under pathological conditions. In this review, we integrate current information about the classification, biogenesis, and function of ncRNAs and how these ncRNAs support skeletal development through their regulation of critical genes and signaling pathways in vivo. We also summarize the updated knowledge of ncRNAs involved in common skeletal diseases and disorders, including but not limited to osteoporosis, osteoarthritis, rheumatoid arthritis, scoliosis, and intervertebral disc degeneration, by highlighting their roles established from in vivo, in vitro, and ex vivo studies.
Keyphrases
- gene expression
- rheumatoid arthritis
- genome wide
- signaling pathway
- dna methylation
- endothelial cells
- healthcare
- machine learning
- postmenopausal women
- copy number
- disease activity
- deep learning
- transcription factor
- single cell
- stem cells
- oxidative stress
- cell death
- knee osteoarthritis
- epithelial mesenchymal transition
- cell proliferation
- mesenchymal stem cells
- health information
- systemic lupus erythematosus
- ankylosing spondylitis
- pi k akt
- high resolution
- case control
- protein protein