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Updated: May 4, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
Identification and characterization of microRNAs in the crab-eating macaque (Macaca fascicularis) using transcriptome
Hao Yang1, Rui Zhang1, Ying Jing1
1Jiangsu Engineering Research Center for microRNA Biology and Biotechnology, State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, 22 Hankou Road, Nanjing 210093, China.
Abstract:
MicroRNAs (miRNAs), with an average length between 16 nt and 26 nt, are small non-coding RNAs that can repress gene expression on the post-transcriptional level. Macaca fascicularis (M. fascicularis), one of the most important nonhuman primate animal models, is widely used in basic and applied preclinical research, especially in studies that involve neuroscience and disease. However, due to the lack of a complete genome sequence, the miRNAs in M. fascicularis have not been completely characterized. In this study, 86 putative M. fascicularis miRNAs were identified using a strategy of our design. The expression of some of these miRNAs in the tissue was confirmed by qRT-PCR. The function and pathway of their targeted genes were analyzed to reveal the potential relevance of miRNA regulation on diseases and physiological processes. The current study provides insight into potential miRNAs and forms a useful knowledge base for the future understanding of the function of miRNAs in M. fascicularis.
Insights
Researchers identified 86 novel microRNAs (miRNAs) in Macaca fascicularis, a key nonhuman primate model. This discovery advances understanding of miRNA regulation in neuroscience and disease research.
Area of Science:
- Molecular Biology
- Genomics
- Noncoding RNA Biology
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression post-transcriptionally.
- Macaca fascicularis is a crucial nonhuman primate model in preclinical research, particularly for neuroscience and disease.
- Characterization of M. fascicularis miRNAs is incomplete due to a lack of a complete genome sequence.
Purpose of the Study:
- To identify novel microRNAs (miRNAs) in Macaca fascicularis.
- To establish a foundational knowledge base for M. fascicularis miRNA function.
- To explore the potential roles of identified miRNAs in physiological processes and diseases.
Main Methods:
- Development of a proprietary strategy for miRNA identification.
- Utilizing quantitative real-time PCR (qRT-PCR) for expression validation.
- Bioinformatic analysis of target gene functions and pathways.
Main Results:
- Identification of 86 putative Macaca fascicularis miRNAs.
- Confirmation of expression for selected miRNAs via qRT-PCR.
- Analysis revealed potential involvement of miRNA targets in disease and physiological processes.
Conclusions:
- This study successfully identified a significant number of novel miRNAs in M. fascicularis.
- The findings provide a valuable resource for future research on miRNA functions in this primate model.
- Understanding these miRNAs can offer insights into primate biology and disease mechanisms.
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