Interaction between the motor protein prestin and the transporter protein VAPA

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1803, Issue 7, 2010, Pages 796-804

  Sengupta, Soma ^a   Miller, Katharine K ^a   Homma, Kazuaki ^b   Edge, Roxanne ^b   Cheatham, Mary Ann ^b   Dallos, Peter ^b   Zheng, Jing ^a,b  

^a NORTHWESTERN UNIVERSITY   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Outer hair cell; Prestin; Protein trafficking; VAPA

Indexed keywords

COMPLEMENTARY DNA; PRESTIN; SYNAPTOBREVIN ASSOCIATED PROTEIN A; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL MEMBRANE; CELLULAR STRESS SIGNAL; CONTROLLED STUDY; DNA LIBRARY; ENDOPLASMIC RETICULUM; HAIR CELL; HOMEOSTASIS; IMMUNOPRECIPITATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN TARGETING; PROTEIN TRANSPORT; TWO HYBRID SYSTEM; WILD TYPE;

ANIMALS; CARRIER PROTEINS; CELL LINE; CELL MEMBRANE; GENE LIBRARY; HAIR CELLS, AUDITORY, OUTER; HUMANS; MEMBRANE PROTEINS; MICE; MOLECULAR MOTOR PROTEINS; RECOMBINANT FUSION PROTEINS; TWO-HYBRID SYSTEM TECHNIQUES;

MUS;

EID: 77953364152     PISSN: 01674889     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2010.03.017     Document Type: Article

References (41)

1. Dallos P. The active cochlea. J. Neurosci. 1992, 12:4575-4585.
2. Ryan A., Dallos P. Effect of absence of cochlear outer hair cells on behavioural auditory threshold. Nature 1975, 253:44-46.
3. Dallos P., Harris D. Properties of auditory nerve responses in absence of outer hair cells. J. Neurophysiol. 1978, 41:365-383.
4. Harrison R.V., Evans E.F. Cochlear fibre responses in guinea pigs with well defined cochlear lesions. Scand. Audiol. Suppl. 1979, 83-92.
5. Dallos P., Harris D.M., Relkin E., Cheatham M.A. Two-tone suppression and intermodulation distortion in the cochlea: effect of outer hair cell lesions. Delft University Press 1980.
6. Brownell W.E., Bader C.R., Bertrand D., de Ribaupierre Y. Evoked mechanical responses of isolated cochlear outer hair cells. Science 1985, 227:194-196.
7. Santos-Sacchi J., Dilger J.P. Whole cell currents and mechanical responses of isolated outer hair cells. Hear. Res. 1988, 35:143-150.
8. He D.Z., Dallos P. Somatic stiffness of cochlear outer hair cells is voltage-dependent. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:8223-8228.
9. Evans B.N., Dallos P. Stereocilia displacement induced somatic motility of cochlear outer hair cells. Proc. Natl. Acad. Sci. U. S. A. 1993, 90:8347-8351.
10. Zheng J., Shen W., He D.Z., Long K.B., Madison L.D., Dallos P. Prestin is the motor protein of cochlear outer hair cells. Nature 2000, 405:149-155.
11. Dallos P., Zheng J., Cheatham M.A. Prestin and the cochlear amplifier. J. Physiol. 2006, 576:37-42.
12. Dallos P., et al. Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron 2008, 58:333-339.
13. Liberman M.C., Gao J., He D.Z., Wu X., Jia S., Zuo, Zuo J. Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier. Nature 2002, 419:300-304.
14. Cheatham M.A., Hheauynh K.H., Gao J., Zuo J., Dallos P. Cochlear function in Prestin knockout mice. J. Physiol. 2004, 560:821-830.
15. Cheatham M.A., et al. Evaluation of an independent prestin mouse model derived from the 129S1 strain. Audiol. Neurootol. 2007, 12:378-390.
16. Rajagopalan L., et al. Tuning of the outer hair cell motor by membrane cholesterol. J. Biol. Chem. 2007, 282:36659-36670.
17. Holley M.C. The Cochlea: The Springer Handbook of Auditory Research 1996, Springer, New York.
18. Zheng J., Du G.G., Anderson C.T., Keller J.P., Orem A., Dallos P., Cheatham M. Analysis of the oligomeric structure of the motor protein prestin. J. Biol. Chem. 2006, 281:19916-19924.
19. Zheng J., Long K.B., Matsuda K.B., Madison L.D., Ryan A.D., Dallos P.D. Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells. Mamm. Genome 2003, 14:87-96.
20. Zheng J., et al. The C-terminus of prestin influences nonlinear capacitance and plasma membrane targeting. J. Cell Sci. 2005, 118:2987-2996.
21. Skehel P.A., Martin K.C., Kandel E.R., Bartsch D. A VAMP-binding protein from Aplysia required for neurotransmitter release. Science 1995, 269:1580-1583.
22. Nishimura Y., Hayashi M., Inada H., Tanaka T. Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins. Biochem. Biophys. Res. Commun. 1992, 254:21-26.
23. Skehel P.A., Fabian-Fine R., Kandel E.R. Mouse VAP33 is associated with the endoplasmic reticulum and microtubules. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:1101-1106.
24. Wyles J.P., McMaster C.R., Ridgway N.D. Vesicle-associated membrane protein-associated protein-A (VAP-A) interacts with the oxysterol-binding protein to modify export from the endoplasmic reticulum. J. Biol. Chem. 2002, 277:29908-29918.
25. Kawano M., Kumagai K., Nishijima M., Hanada K. Efficient trafficking of ceramide from the endoplasmic reticulum to the Golgi apparatus requires a VAMP-associated protein-interacting FFAT motif of CERT. J. Biol. Chem. 2006, 281:30279-30288.
26. Loewen C.J., Roy, Roy A., Levine T.P. A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP. Embo J. 2003, 22:2025-2035.
27. Wyles J.P., Ridgway N.D. VAMP-associated protein-A regulates partitioning of oxysterol-binding protein-related protein-9 between the endoplasmic reticulum and Golgi apparatus. Exp. Cell Res. 2004, 297:533-547.
28. Teuling E., Ahmed S., Haasdijk E., Demmers J., Steinmetz M.O., Akhmanova A., Jaarsma D., Hoogenraad C.C. Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates. J. Neurosci. 2007, 27:9801-9815.
29. Ettayebi K., Hardy M.E. Norwalk virus nonstructural protein p48 forms a complex with the SNARE regulator VAP-A and prevents cell surface expression of vesicular stomatitis virus G protein. J. Virol. 2003, 77:11790-11797.
30. Gkogkas C., Middleton S., Kremer A.M., Wardrope C., Hannah M., Gillingwater T.H., Skehel P. VAPB interacts with and modulates the activity of ATF6. Hum. Mol. Genet. 2008, 17:1517-1526.
31. Foster L.J., Weir M.L., Lim D.Y., Liu Z., Trimble W.S., Klip A. A functional role for VAP-33 in insulin-stimulated GLUT4 traffic. Traffic 2000, 1:512-521.
32. Zheng J., Anderson C.T., Miller K.K., Cheatham M., Dallos P. Identifying components of the hair-cell interactome involved in cochlear amplification. B.M.C. Genomics 2009, 10:127.
33. Matsuda K., Zheng J., Du G.G., Klocker N., Madison L.D., Dallos P. N-linked glycosylation sites of the motor protein prestin: effects on membrane targeting and electrophysiological function. J. Neurochem. 2004, 89:928-938.
34. Cheatham M.A., Zheng J., Huynh K.H., Du G.G., Gao J., Zuo J., Navarrete E., Dallos P. Cochlear function in mice with only one copy of the prestin gene. J. Physiol. 2005, 569:229-241.
35. Brunette D.M., Till J.E. A rapid method for the isolation of L-cell surface membranes using an aqueous two-phase polymer system. J. Membr. Biol. 1971, 5:215-224.
36. Belyantseva I.A., Adler H.J., Curi R., Frolenkov G.I., Kachar B. Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells. J. Neurosci. 2000, 20:RC116.
37. Wu X., Gao J., Guo Y., Zuo J. Hearing threshold elevation precedes hair-cell loss in prestin knockout mice. Brain Res. Mol. Brain Res. 2004, 126:30-37.
38. Montcouquiol M., et al. Asymmetric localization of Vangl2 and Fz3 indicate novel mechanisms for planar cell polarity in mammals. J. Neurosci. 2006, 26:5265-5275.
39. Wang Y., Guo N., Nathans J. The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J. Neurosci. 2006, 26:2147-2156.
40. Nagy I., Bodmer M., Schmid S., Bodmer D. Promyelocytic leukemia zinc finger protein localizes to the cochlear outer hair cells and interacts with prestin, the outer hair cell motor protein. Hear. Res. 2005, 204:216-222.
41. Zhang K., Kaufman R.J. Identification and characterization of endoplasmic reticulum stress-induced apoptosis in vivo. Methods Enzymol. 2008, 442:395-419.