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Published on: July 30, 2011
Expression profile analysis of long non-coding RNA in skeletal muscle of osteoporosis by microarray and
Shaojin Liu1, Hongxing Huang2, Shuang Chai1
11Guangzhou University of Chinese Medicine, Guangzhou, 510405 China.
Background:
Osteoporosis (OP) is a condition featured by bone mass loss and bone tissue microarchitectural alterations due to impaired tissue homeostasis favoring excessive bone resorption versus deposition. The trigger of such an impairment and the downstream molecular pathways involved are yet to be clarified. Long non-coding RNA (lncRNA) plays a role in gene transcription, protein expression and epigenetic regulation; and altered expression results in immune or metabolism related desease development. To determine whether lncRNAs are involved in osteoporosis, we analyzed the expression profile of lncRNAs and mRNAs in osteoporosis.
Method:
Three pairs of osteoporosis patients (OP group) and healthy people controls (NC group) were screened by microarray. Quantitative polymerase chain reaction (qRT-PCR) was performed to confirm dysregulated lncRNA expressions in 5 pairs of OP and NC group tissues samples. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to construct the lncRNA-mRNA co-expression network.
Result:
Through co-expression analysis, differently expressed transcripts were divided into modules, and lncRNAs were functionally annotated. We further analyzed the clinical significance of crucial lncRNAs from modules in public data. Finally, the expression of five lncRNAs, CUST_44695_PI430048170-GeneSymbol:CTA-384D8.35;CUST_39447_PI430048170,CUST_73298_PI430048170,CUST_108340_PI430048170,CUST_118927_PI430048170,this four lncRNAs have not been annotation genes and have not found GeneSymbols, and by quantitative RT-PCR, which may be associated with osteoporosis patients' overall survival.
Conclusion:
Analysis of this study revealed that dysregulated lncRNAs and mRNAs in osteoporosis patients and health people controls could affect the immune or metabolism system and musculoskeletal cell differentiation. The biological functions of those lncRNAs need to be further validated.
Insights
Long non-coding RNAs (lncRNAs) are implicated in osteoporosis, a condition of bone loss. Dysregulated lncRNAs and messenger RNAs (mRNAs) in osteoporosis patients may impact immune and metabolic systems, influencing bone health.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- Osteoporosis (OP) is characterized by reduced bone mass and microarchitectural deterioration, stemming from imbalanced bone remodeling.
- The precise molecular triggers and pathways underlying OP pathogenesis remain incompletely understood.
- Long non-coding RNAs (lncRNAs) are key regulators of gene expression and epigenetic processes; their aberrant expression is linked to various diseases, including immune and metabolic disorders.
Purpose of the Study:
- To investigate the involvement of lncRNAs in the molecular mechanisms of osteoporosis.
- To identify differentially expressed lncRNAs and messenger RNAs (mRNAs) in osteoporosis patients compared to healthy controls.
Main Methods:
- Microarray analysis was employed to profile lncRNA and mRNA expression in three pairs of osteoporosis patients and healthy controls.
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to validate the expression of dysregulated lncRNAs in five independent sample pairs.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to construct a lncRNA-mRNA co-expression network.
Main Results:
- Co-expression analysis identified distinct modules of differentially expressed transcripts, with functional annotation of lncRNAs.
- Clinical significance analysis of key lncRNAs from these modules was conducted using public datasets.
- Quantitative RT-PCR confirmed the altered expression of five specific lncRNAs, some lacking established gene symbols, in osteoporosis tissues, suggesting a potential association with patient survival.
Conclusions:
- Dysregulated lncRNAs and mRNAs in osteoporosis are associated with alterations in immune and metabolic systems, as well as musculoskeletal cell differentiation.
- The identified lncRNAs represent potential novel biomarkers or therapeutic targets for osteoporosis.
- Further experimental validation is required to elucidate the precise biological functions of these dysregulated lncRNAs in osteoporosis.
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