CLIC5

Chloride intracellular channel protein 5 is a protein that in humans is encoded by the CLIC5 gene.[5][6]

CLIC5
Identifiers
AliasesCLIC5, MST130, MSTP130, DFNB102, DFNB103, chloride intracellular channel 5
External IDsOMIM: 607293 MGI: 1917912 HomoloGene: 987 GeneCards: CLIC5
Gene location (Human)
Chr.Chromosome 6 (human)[1]
Band6p21.1Start45,880,827 bp[1]
End46,080,348 bp[1]
RNA expression pattern


More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

53405

224796

Ensembl

ENSG00000112782

ENSMUSG00000023959

UniProt

Q9NZA1
Q53G01
Q49AE1

Q8BXK9

RefSeq (mRNA)

NM_001114086
NM_001256023
NM_016929
NM_001370649
NM_001370650

NM_172621

RefSeq (protein)

NP_766209

Location (UCSC)Chr 6: 45.88 – 46.08 MbChr 17: 44.13 – 44.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Expression and localization

CLIC5 exists in two alternative splice variants, a smaller CLIC5A and larger CLIC5B protein.

CLIC5A is expressed chiefly in the renal glomerulus, specifically in podocytes. Within the cell, CLIC5A is localized to the plasma membrane and the cytosol, and associates and is regulated by the actin cytoskeleton.[6] CLIC5A can form ion channels in vitro and its channel activity is regulated by actin, though measurement of its chloride conductance in vitro suggests that CLIC5A is equally selective for cations and anions.

Function

Although chloride intracellular channel (CLIC) proteins were thought to be involved in ion transport in subcellular compartments, their actual functions suggest their role in diverse cellular and physiological functions including apoptosis and angiogenesis in CLIC1.

CLIC5A, through its interactions with the small GTPase Rac1, induces the phosphorylation of ezrin-moeisin-radixin (ERM) proteins and localized production of the phosphoinositide phosphatidylinositol-4,5-bisphosphate.[7] These two events activate ezrin, enabling it to couple transmembrane proteins to the actin cytoskeleton, which could represent a mechanism by which podocyte foot processes form to enable renal filtration.[8]

Clinical relevance

CLIC5A deficiency in mouse models potentiates glomerular injury in hypertension. In these mice, podocyte foot processes were also more sparse and disperse than in wild-type mice.[8]

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gollark: I don't really understand what you mean by that?
gollark: Please explain ”linear transformation”.
gollark: Apiologically gradientous.
gollark: The jabuapiolic algorithm?

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000112782 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000023959 - 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. Berryman M, Bretscher A (May 2000). "Identification of a novel member of the chloride intracellular channel gene family (CLIC5) that associates with the actin cytoskeleton of placental microvilli". Molecular Biology of the Cell. 11 (5): 1509–21. doi:10.1091/mbc.11.5.1509. PMC 14863. PMID 10793131.
  6. "Entrez Gene: CLIC5 chloride intracellular channel 5".
  7. Al-Momany A, Li L, Alexander RT, Ballermann BJ (December 2014). "Clustered PI(4,5)P₂ accumulation and ezrin phosphorylation in response to CLIC5A". Journal of Cell Science. 127 (Pt 24): 5164–78. doi:10.1242/jcs.147744. PMID 25344252.
  8. Tavasoli M, Li L, Al-Momany A, Zhu LF, Adam BA, Wang Z, Ballermann BJ (April 2016). "The chloride intracellular channel 5A stimulates podocyte Rac1, protecting against hypertension-induced glomerular injury". Kidney International. 89 (4): 833–47. doi:10.1016/j.kint.2016.01.001. PMID 26924049.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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