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MiR-146

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miR-146
File:Mir-146 SS.png
Conserved secondary structure of miR-146 microRNA precursor
Identifiers
SymbolmiR-146
Alt. SymbolsMIR146
RfamRF00691
miRBaseMI0000477
miRBase familyMIPF0000103
Entrez406938
HUGO31533
OMIM610566
RefSeqNR_029897
Other data
RNA typemiRNA
Domain(s)Mammalia
GO0035195
SO0001244
LocusChr. 5 q34
PDB structuresPDBe

miR-146 is a family of microRNA precursors found in mammals, including humans. The ~22 nucleotide mature miRNA sequence is excised from the precursor hairpin by the enzyme Dicer.[1] This sequence then associates with RISC which effects RNA interference.[2]

miR-146 is primarily involved in the regulation of inflammation and other process that function in the innate immune system.[3] Loss of functional miR-146 (and mir-145) could predispose an individual to suffer from chromosome 5q deletion syndrome.[4] miR-146 has also been reported to be highly upregulated in osteoarthritis cartilage, and could be involved in its pathogenesis.[5] mir-146 expression is associated with survival in triple negative breast cancer.[6]

Function[edit | edit source]

miR-146 is thought to be a mediator of inflammation along with another microRNA, mir-155. The expression of miR-146 is upregulated by inflammatory factors such as interleukin 1 and tumor necrosis factor-alpha.[7] miR-146 dysregulates a number of targets which are mostly involved in toll-like receptor pathways that bring about a cytokine response as part of the innate immune system.[3][7] miR-146 operates in a feedback system or "negative regulatory loop"[8] to finely tune inflammatory responses.[4]

Applications[edit | edit source]

miR-146 could be used as a biomarker for sepsis.[9] In addition it was found to be absent from the exosomes of prion infected cells suggesting it could be used as a biomarker for prion infection.[10] miR-146a could be targeted therapeutically as its depletion has implication in the hyperactive response to infection.[11]

References[edit | edit source]

  1. ↑ Ambros V (Dec 2001). "microRNAs: tiny regulators with great potential". Cell. 107 (7): 823–6. doi:10.1016/S0092-8674(01)00616-X. PMID 11779458.
  2. ↑ Gregory RI, Chendrimada TP, Cooch N, Shiekhattar R (Nov 2005). "Human RISC couples microRNA biogenesis and posttranscriptional gene silencing". Cell. 123 (4): 631–40. doi:10.1016/j.cell.2005.10.022. PMID 16271387.
  3. ↑ 3.0 3.1 Sonkoly E, Ståhle M, Pivarcsi A (Apr 2008). "MicroRNAs and immunity: novel players in the regulation of normal immune function and inflammation". Seminars in Cancer Biology. 18 (2): 131–40. doi:10.1016/j.semcancer.2008.01.005. PMID 18291670.
  4. ↑ 4.0 4.1 Quinn SR, O'Neill LA (Jul 2011). "A trio of microRNAs that control Toll-like receptor signalling". International Immunology. 23 (7): 421–5. doi:10.1093/intimm/dxr034. PMID 21652514.
  5. ↑ Yamasaki K, Nakasa T, Miyaki S, Ishikawa M, Deie M, Adachi N, Yasunaga Y, Asahara H, Ochi M (Apr 2009). "Expression of MicroRNA-146a in osteoarthritis cartilage". Arthritis and Rheumatism. 60 (4): 1035–41. doi:10.1002/art.24404. PMC 2670476. PMID 19333945.
  6. ↑ Lánczky, András; Nagy, Ádám; Bottai, Giulia; Munkácsy, Gyöngyi; Szabó, András; Santarpia, Libero; Győrffy, Balázs (2016-12-01). "miRpower: a web-tool to validate survival-associated miRNAs utilizing expression data from 2178 breast cancer patients". Breast Cancer Research and Treatment. 160 (3): 439–446. doi:10.1007/s10549-016-4013-7. ISSN 1573-7217. PMID 27744485.
  7. ↑ 7.0 7.1 Sheedy FJ, O'Neill LA (Dec 2008). "Adding fuel to fire: microRNAs as a new class of mediators of inflammation". Annals of the Rheumatic Diseases. 67 Suppl 3: iii50–5. doi:10.1136/ard.2008.100289. PMID 19022814.
  8. ↑ Ma X, Becker Buscaglia LE, Barker JR, Li Y (Jun 2011). "MicroRNAs in NF-kappaB signaling". Journal of Molecular Cell Biology. 3 (3): 159–66. doi:10.1093/jmcb/mjr007. PMC 3104013. PMID 21502305.
  9. ↑ Gîză DE, Vasilescu C (Sep–Oct 2010). "[MicroRNA's role in sepsis and endotoxin tolerance. More players on the stage]". Chirurgia. 105 (5): 625–30. PMID 21141085.
  10. ↑ Bellingham SA, Coleman BM, Hill AF (Nov 2012). "Small RNA deep sequencing reveals a distinct miRNA signature released in exosomes from prion-infected neuronal cells". Nucleic Acids Research. 40 (21): 10937–49. doi:10.1093/nar/gks832. PMC 3505968. PMID 22965126.
  11. ↑ O'Connell RM, Rao DS, Baltimore D (2012). "microRNA regulation of inflammatory responses". Annual Review of Immunology. 30: 295–312. doi:10.1146/annurev-immunol-020711-075013. PMID 22224773.

Further reading[edit | edit source]

See also[edit | edit source]

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