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    MCOLN3 mucolipin TRP cation channel 3 [ Homo sapiens (human) ]

    Gene ID: 55283, updated on 3-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    palmitoylation is a prerequisite for the function of MCOLN3/TRPML3 as a Ca(2+) channel in autophagosome formation.

    Palmitoylation controls trafficking of the intracellular Ca(2+) channel MCOLN3/TRPML3 to regulate autophagy.
    Kim SW, Kim DH, Park KS, Kim MK, Park YM, Muallem S, So I, Kim HJ., Free PMC Article

    03/7/2020
    The work elucidates the molecular architecture and provides insights into how multiple ligands regulate TRPML1 and TRPML3. (Review)

    The regulatory mechanism of mammalian TRPMLs revealed by cryo-EM.
    Schmiege P, Fine M, Li X., Free PMC Article

    06/1/2019
    these results suggest that TRPML3 plays a role in autophagosome maturation through the interaction with GATE16, by providing Ca(2+) in the fusion process.

    The Ca2+ channel TRPML3 specifically interacts with the mammalian ATG8 homologue GATE16 to regulate autophagy.
    Choi S, Kim HJ.

    05/10/2014
    TRPML3 and TRPV5 heteromers could have a biological function

    A novel ion channel formed by interaction of TRPML3 with TRPV5.
    Guo Z, Grimm C, Becker L, Ricci AJ, Heller S., Free PMC Article

    08/31/2013
    Negatively charged amino acids in the extracellular loops of TRPML3 may interfere with the observed sodium inhibition.

    Constitutive activity of TRPML2 and TRPML3 channels versus activation by low extracellular sodium and small molecules.
    Grimm C, Jörs S, Guo Z, Obukhov AG, Heller S., Free PMC Article

    09/15/2012
    TRPML 1, 2 and 3 assemblies regulated cell viability and starvation-induced autophagy.

    Heteromultimeric TRPML channel assemblies play a crucial role in the regulation of cell viability models and starvation-induced autophagy.
    Zeevi DA, Lev S, Frumkin A, Minke B, Bach G., Free PMC Article

    01/1/2011
    analysis of the TRPML3 channel pore and its stable expansion by the Varitint-Waddler-causing mutation

    Properties of the TRPML3 channel pore and its stable expansion by the Varitint-Waddler-causing mutation.
    Kim HJ, Yamaguchi S, Li Q, So I, Muallem S., Free PMC Article

    06/28/2010
    Data show that TRPMLs form distinct functional channel complexes.

    Functional multimerization of mucolipin channel proteins.
    Curcio-Morelli C, Zhang P, Venugopal B, Charles FA, Browning MF, Cantiello HF, Slaugenhaupt SA.

    01/21/2010
    Results show that mucolipin 3 is a novel calcium channel that plays a crucial role in the regulation of cargo trafficking along the endosomal pathway.

    The calcium channel mucolipin-3 is a novel regulator of trafficking along the endosomal pathway.
    Martina JA, Lelouvier B, Puertollano R., Free PMC Article

    01/21/2010
    These findings reveal a prominent role for TRPML3 in regulating endocytosis, membrane trafficking and autophagy, perhaps by controlling the Ca(2+) in the vicinity of cellular organelles that is necessary to regulate these cellular events.

    The Ca(2+) channel TRPML3 regulates membrane trafficking and autophagy.
    Kim HJ, Soyombo AA, Tjon-Kon-Sang S, So I, Muallem S., Free PMC Article

    01/21/2010
    The deaf-waddler isoform of PMCA2, operating at 30% efficacy, showed a significantly decreased ability to rescue the Ca(2+) loading of cells expressing TRPML3(A419P).

    Life and death of sensory hair cells expressing constitutively active TRPML3.
    Grimm C, Jörs S, Heller S., Free PMC Article

    01/21/2010
    First characterization of wild-type TRPML3 calcium-permeable channel properties and its regulation by extracytosolic (luminal)hydrogen ion (H+).

    A novel mode of TRPML3 regulation by extracytosolic pH absent in the varitint-waddler phenotype.
    Kim HJ, Li Q, Tjon-Kon-Sang S, So I, Kiselyov K, Soyombo AA, Muallem S., Free PMC Article

    01/21/2010
    The A419P mutation affects TRPLMe channel glycosylation and causes massive cell death

    Gain-of-function mutation in TRPML3 causes the mouse Varitint-Waddler phenotype.
    Kim HJ, Li Q, Tjon-Kon-Sang S, So I, Kiselyov K, Muallem S.

    01/21/2010
    TRPML3(A419P) and (I362T+A419P) at physiological potentials may have a role in hair cell degeneration and deafness

    The varitint-waddler (Va) deafness mutation in TRPML3 generates constitutive, inward rectifying currents and causes cell degeneration.
    Nagata K, Zheng L, Madathany T, Castiglioni AJ, Bartles JR, García-Añoveros J., Free PMC Article

    01/21/2010
    there is a hierarchy controlling the subcellular distributions of the TRPMLs such that TRPML1 and TRPML2 dictate the localization of TRPML3 and not vice versa

    Lysosomal localization of TRPML3 depends on TRPML2 and the mucolipidosis-associated protein TRPML1.
    Venkatachalam K, Hofmann T, Montell C., Free PMC Article

    01/21/2010
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