Related Experiment Video
Updated: Mar 16, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
Natural Functional SNPs in miR-155 Alter Its Expression Level, Blood Cell Counts, and Immune Responses
Congcong Li1, Huabin He2, An Liu3
1Key Laboratory of Agricultural Animal Genetics, Breeding, and Reproduction of the Ministry of Education, Huazhong Agricultural University, Wuhan, China; Key Laboratory of Swine Genetics and Breeding of the Ministry of Agriculture, Huazhong Agricultural University, Wuhan, China; College of Animal Science and Technology, Henan University of Animal Husbandry and Economy, Zhengzhou, China.
Abstract:
miR-155 has been confirmed to be a key factor in immune responses in humans and other mammals. Therefore, investigation of variations in miR-155 could be useful for understanding the differences in immunity between individuals. In this study, four SNPs in miR-155 were identified in mice (Mus musculus) and humans (Homo sapiens). In mice, the four SNPs were closely linked and formed two miR-155 haplotypes (A and B). Ten distinct types of blood parameters were associated with miR-155 expression under normal conditions. Additionally, 4 and 14 blood parameters were significantly different between these two genotypes under normal and lipopolysaccharide (LPS) stimulation conditions, respectively. Moreover, the expression levels of miR-155, the inflammatory response to LPS stimulation, and the lethal ratio following Salmonella typhimurium infection were significantly increased in mice harboring the AA genotype. Further, two SNPs, one in the loop region and the other near the 3' terminal of pre-miR-155, were confirmed to be responsible for the differential expression of miR-155 in mice. Interestingly, two additional SNPs, one in the loop region and the other in the middle of miR-155*, modulated the function of miR-155 in humans. Predictions of secondary RNA structure using RNAfold showed that these SNPs affected the structure of miR-155 in both mice and humans. Our results provide novel evidence of the natural functional SNPs of miR-155 in both mice and humans, which may affect the expression levels of mature miR-155 by modulating its secondary structure. The SNPs of human miR-155 may be considered as causal mutations for some immune-related diseases in the clinic. The two genotypes of mice could be used as natural models for studying the mechanisms of immune diseases caused by abnormal expression of miR-155 in humans.
Insights
Single nucleotide polymorphisms (SNPs) in microRNA-155 (miR-155) influence immune responses in mice and humans. These miR-155 genetic variations impact blood parameters and inflammatory responses, offering insights into immune-related diseases.
Area of Science:
- Genetics
- Immunology
- Molecular Biology
Background:
- MicroRNA-155 (miR-155) is a critical regulator of immune responses in mammals.
- Understanding genetic variations in miR-155 can elucidate individual differences in immunity.
- Single nucleotide polymorphisms (SNPs) are common genetic variations that can alter gene function.
Purpose of the Study:
- To identify and characterize functional SNPs in miR-155 in mice and humans.
- To investigate the impact of these SNPs on miR-155 expression and immune parameters.
- To explore the potential of these SNPs as markers for immune-related diseases.
Main Methods:
- Identification of four SNPs in miR-155 in mice and humans.
- Genotyping of mice and analysis of blood parameters under normal and lipopolysaccharide (LPS) stimulated conditions.
- Assessment of inflammatory response, survival rates after infection, and secondary RNA structure predictions using RNAfold.
- Analysis of SNPs in pre-miR-155 and miR-155* regions.
Main Results:
- Four linked SNPs in mice formed two haplotypes, associated with differential blood parameters and immune responses.
- Mice with the AA genotype exhibited increased miR-155 expression, heightened inflammatory response to LPS, and higher mortality after Salmonella typhimurium infection.
- Two SNPs in mice and two in humans were identified as responsible for differential miR-155 expression and function by affecting secondary RNA structure.
- Human miR-155 SNPs may serve as causal mutations for immune-related diseases.
Conclusions:
- Natural functional SNPs in miR-155 exist in both mice and humans, modulating mature miR-155 expression via secondary structure changes.
- These findings highlight the role of miR-155 genetic variations in immune system regulation.
- Mouse models with distinct miR-155 genotypes can be valuable for studying immune diseases linked to aberrant miR-155 expression.
More Related Videos
Related Concept Videos
MicroRNAs
MicroRNAs
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

