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The function of vacuolar ATPase (V-ATPase) a subunit isoforms in invasiveness of MCF10a and MCF10CA1a human breast cancer cells.
Inhibition of lysosome degradation on autophagosome formation and responses to GMI, an immunomodulatory protein from Ganoderma microsporum. ATP6V0A1 plays an important role in mediating autophagosome-lysosome fusion.
a series of events whereby ATP6V0A1 3'-UTR variant T+3246C functioned: ATP6V0A1 expression probably was affected through differential micro-RNA effects, altering vacuolar pH and consequently CHGA (show CHGA Proteins) processing and exocytotic secretion.
The mRNA levels of POLR2F (show POLR2F Proteins), ATP6V0A1 and PRNP (show PRNP Proteins) were evaluated by quantitative RT-PCR in 70 colorectal carcinomas and 17 normal tissue specimens and were correlated with clinicopathological parameters.
These results suggest that the Golgi complex may serve as a membrane platform for noncanonical autophagy where V-ATPase (show ATP6V1H Proteins) is (show ATP11A Proteins) a key player.
Data suggest a mechanism by which betaA3/A1-crystallin regulates lysosomal function by modulating the activity of V-ATPase (show ATP6V1H Proteins).
demonstrated that CRYBA1 coimmunoprecipitates with the ATP6V0A1/V0-ATPase a1 subunit
V-ATPase (show ATP6V1H Proteins) membrane domain would allow the exocytotic machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmitter reloading.
This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor-mediated endocytosis, and synaptic vesicle proton gradient generation. V-ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain consists of three A and three B subunits, two G subunits plus the C, D, E, F, and H subunits. The V1 domain contains the ATP catalytic site. The V0 domain consists of five different subunits: a, c, c', c', and d. Additional isoforms of many of the V1 and V0 subunit proteins are encoded by multiple genes or alternatively spliced transcript variants. This gene encodes one of three A subunit proteins and the encoded protein is associated with clathrin-coated vesicles. Three transcript variants encoding different isoforms have been found for this gene.
V-ATPase 116 kDa
, V-type proton ATPase 116 kDa subunit a
, V-type proton ATPase 116 kDa subunit a isoform 1
, vacuolar proton translocating ATPase 116 kDa subunit a
, vacuolar H(+)-transporting ATPase 116 kDa subunit, a1 isoform
, ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1A (110/116kD)
, ATPase, H+ transporting, lysosomal non-catalytic accessory protein 1 (110/116kD)
, H(+)-transporting two-sector ATPase, 116 kDa accessory protein A1
, clathrin-coated vesicle/synaptic vesicle proton pump 116 kDa subunit
, vacuolar adenosine triphosphatase subunit Ac116
, vacuolar proton pump subunit 1
, vacuolar proton pump, subunit 1
, vacuolar proton translocating ATPase 116 kDa subunit A
, vacuolar-type H(+)-ATPase 115 kDa subunit
, ATPase, H+ transporting, lysosomal (vacuolar proton pump) noncatalytic accessory protein 1 (110/160 kDa)
, ATPase, H+ transporting, lysosomal (vacuolar proton pump) noncatalytic accessory protein 1A (110/160 kDa)
, ATPase, H+ transporting, lysosomal V0 subunit a
, V-ATPase a1
, ATPase H+ transporting lysosomal (vacuolar proton pump) noncatalytic accessory protein 1 (110/160 kDa)
, ATPase, H+ transporting, lysosomal noncatalytic accessory protein 1a
, v-H+ATPase subunit a1