Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.6.1.3 (
ATPase
)
65,361
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Sensory hair cells require control of physical properties of their apical plasma membranes for normal development and function. Members of the ADP-ribosylation factor (ARF) small GTPase family regulate membrane trafficking and cytoskeletal assembly in many cells. We identified
ELMO domain-containing protein 1
(
ELMOD1
), a guanine nucleoside
triphosphatase
activating protein (GAP) for ARF6, as the most highly enriched ARF regulator in hair cells. To characterize
ELMOD1
control of trafficking, we analyzed mice of both sexes from a strain lacking functional
ELMOD1
[roundabout (
rda
)]. In
rda/rda
mice, cuticular plates of utricle hair cells initially formed normally, then degenerated after postnatal day 5; large numbers of vesicles invaded the compromised cuticular plate. Hair bundles initially developed normally, but the cell's apical membrane lifted away from the cuticular plate, and stereocilia elongated and fused. Membrane trafficking in type I hair cells, measured by FM1-43 dye labeling, was altered in
rda/rda
mice. Consistent with the proposed GAP role for
ELMOD1
, the ARF6 GTP/GDP ratio was significantly elevated in
rda/rda
utricles compared with controls, and the level of ARF6-GTP was correlated with the severity of the
rda/rda
phenotype. These results suggest that conversion of ARF6 to its GDP-bound form is necessary for final stabilization of the hair bundle.
SIGNIFICANCE STATEMENT
Assembly of the mechanically sensitive hair bundle of sensory hair cells requires growth and reorganization of apical actin and membrane structures. Hair bundles and apical membranes in mice with mutations in the
Elmod1
gene degenerate after formation, suggesting that the
ELMOD1
protein stabilizes these structures. We show that
ELMOD1
is a GTPase-activating protein in hair cells for the small GTP-binding protein ARF6, known to participate in actin assembly and membrane trafficking. We propose that conversion of ARF6 into the GDP-bound form in the apical domain of hair cells is essential for stabilizing apical actin structures like the hair bundle and ensuring that the apical membrane forms appropriately around the stereocilia.
...
PMID:ELMOD1 Stimulates ARF6-GTP Hydrolysis to Stabilize Apical Structures in Developing Vestibular Hair Cells. 2922 2