MicroRNAs in metabolism and metabolic disorders
Open accessAbstract
MicroRNAs (miRNAs) have recently emerged as key regulators of metabolism. For example, miR-33a and miR-33b have a crucial role in controlling cholesterol and lipid metabolism in concert with their host genes, the sterol-regulatory element-binding protein (SREBP) transcription factors. Other metabolic miRNAs, such as miR-103 and miR-107, regulate insulin and glucose homeostasis, whereas miRNAs such as miR-34a are emerging as key regulators of hepatic lipid homeostasis. The discovery of circulating miRNAs has highlighted their potential as both endocrine signalling molecules and disease markers. Dysregulation of miRNAs may contribute to metabolic abnormalities, suggesting that miRNAs may potentially serve as therapeutic targets for ameliorating cardiometabolic disorders.
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miR-33b is found primarily in primates and some other mammals and is absent in commonly used rodent models such as mice and rats.
“Notably, miR-33a is highly conserved across a broad range of species, including rodents, whereas miR-33b is only found primarily in primates and some other mammals, being entirely absent in commonly used rodent models, such as mice and rats.”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [6]
The SREBP–miR-33 regulatory circuit section says rodents lack miR-33b, and the cholesterol-homeostasis section reports miR-33b in non-human primates. The copy does not establish that miR-33b is found primarily in primates and some other mammals, or give a broader species distribution. (LLM, conf=0.85)
Experimental — accuracy not yet measuredmiR-33a and miR-33b are embedded within intronic regions of SREBF genes.
“miR-33a and miR-33b are embedded within the intronic regions of SREBF genes.”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [6]
miR-33b is located within intron 17 of SREBF1.
“In contrast, miR-33b is located within intron 17 of SREBF1, which regulates the expression of genes related to fatty acid and triglyceride homeostasis, such as fatty acid synthase (FASN), acetyl-CoA carboxylase α (ACACA) and stearoyl-CoA desaturase 1 (SCD1) 6 - 8) .”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [6]
miR-33a resides within intron 16 of SREBF2.
“MiR-33a resides within intron 16 of SREBF2, which is primarily involved in the regulation of cholesterol homeostasis genes, such as low-density lipoprotein receptor (LDLR) and 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR).”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [6]
miR-33a is highly conserved across a broad range of species, including rodents.
“Notably, miR-33a is highly conserved across a broad range of species, including rodents, whereas miR-33b is only found primarily in primates and some other mammals, being entirely absent in commonly used rodent models, such as mice and rats.”
From Critical Role of microRNA-33a/b in Cardiovascular and Metabolic Disease: Molecular Mechanisms and Therapeutic Perspectives (2026) · cites this paper as [6]
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- Authors
- Rottiers, V., & Näär, A. M.
- Affiliations
- Massachusetts General Hospital (US)
- Harvard University (US)
- Corresponding author
- Näär, Anders M.
- ORCID
- Näär, Anders M.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2012-03-22
- Volume
- 13
- Issue
- 4
- Pages
- 239-250
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC4021399
- OpenAlex
- W2027744584
- Cited by
- 1,156
- References
- 17
- Citations by year
- 2026: 42 · 2025: 50 · 2024: 44 · 2023: 50 · 2022: 63 · 2021: 87 · 2020: 100 · 2019: 96 · 2018: 105 · 2017: 98 · 2016: 118 · 2015: 100 · 2014: 76 · 2013: 92 · 2012: 34
- FWCI
- 7.33
- Type
- journal article
- Language
- en
- Update notices
- erratum (2012-04-23)
- Open access
- green
- europepmc.org
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R21DK084459, R01DK094184)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- microRNA, metabolism, metabolic disorders, miR-33a, miR-33b, SREBP, cholesterol metabolism, lipid metabolism, insulin, glucose homeostasis, miR-103, miR-107, miR-34a, hepatic lipid homeostasis, circulating microRNAs, disease biomarkers, therapeutic target, cardiometabolic disease
- MeSH terms
- Cholesterol, Endocrine System, Fatty Liver, Glucose, Homeostasis, Humans, Insulin, Metabolic Diseases, Obesity, Signal Transduction, Oligoribonucleotides, Antisense, Metabolic Syndrome, MicroRNAs, Lipid Metabolism, Sterol Regulatory Element Binding Proteins, Non-alcoholic Fatty Liver Disease
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