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Fidgetin-like 2

From Wikipedia, the free encyclopedia
(Redirected from FIGNL2)
FIGNL2
Identifiers
AliasesFIGNL2, fidgetin like 2
External IDsMGI: 3646919; HomoloGene: 28523; GeneCards: FIGNL2; OMA:FIGNL2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001013690
NM_001384995
NM_001384996

NM_001214911

RefSeq (protein)

NP_001013712

NP_001201840

Location (UCSC)Chr 12: 51.82 – 51.85 MbChr 15: 100.95 – 100.98 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Fidgetin-like 2 (FL2) is an enzyme which in humans is encoded by the gene FIGNL2. FL2 slows the rate at which skin cells migrate to wounds to heal them. If this enzyme is suppressed/absent, skin cells move faster, speeding the healing process.[5] FL2 is closely related to another protein called fidgetin (encoded by FIGN in humans), which severs microtubules.[6]

In 2015, researchers disclosed the successful use of nanoparticles to ferry siRNA molecules to their intended targets, reducing healing times in mice with skin excisions or burns. The result was normal, well-orchestrated tissue, including hair follicles and supportive collagen network.[5][7]

References

[edit]
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000261308 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000095440 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 Charafeddine, Rabab A.; Makdisi, J; Schairer, D; O'Rourke, BP; Diaz-Valencia, JD; Chouake, J; Kutner, A; Krausz, A; Adler, B; Nacharaju, P; Liang, H; Mukherjee, S; Friedman, JM; Friedman, A; Nosanchuk, JD; Sharp, DJ (10 March 2015). "Fidgetin-Like 2: A Microtubule-Based Regulator of Wound Healing". The Journal of Investigative Dermatology. 135 (9): 2309–18. doi:10.1038/jid.2015.94. PMC 4537388. PMID 25756798.
  6. Delivery

    Molecules of silencing RNA (siRNA) that bind to a gene's messenger RNA (mRNA) can inhibit the production of FL2, but siRNAs require protection from degradation in order to reach a wound site.<ref name=giz>Moss, Richard (March 30, 2015). "Nanoparticles help wounds to heal 50 percent faster". Gizmag. Retrieved 3 April 2015.
  7. Cite error: The named reference giz was invoked but never defined (see the help page).
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