Two interdependent TRPV channel subunits, inactive and Nanchung, mediate hearing in Drosophila

被引:269
作者
Gong, ZF
Son, WS
Chung, YD
Kim, JW
Shin, DW
McClung, CA
Lee, Y
Lee, HW
Chang, DJ
Kaang, BK
Cho, HW
Oh, U
Hirsh, J [1 ]
Kernan, MJ
Kim, CS
机构
[1] Chonnam Natl Univ, Sch Biol Sci & Tehcnol, Kwangju 500757, South Korea
[2] Univ Virginia, Dept Biol, Charlottesville, VA 22904 USA
[3] Hanwha Chem Co, R&D Ctr, Dept Genet, Taejon 305345, South Korea
[4] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
[5] Seoul Natl Univ, Sch Biol Sci, Natl Res Lab, Seoul 151742, South Korea
[6] Seoul Natl Univ, Sensory Res Ctr, Creat Res Initiat, Seoul 151742, South Korea
[7] Chungnam Natl Univ, Dept Microbiol, Taejon 305764, South Korea
关键词
channel; deafness; Drosophila; hair cell; hearing; mechanosensory;
D O I
10.1523/JNEUROSCI.1645-04.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Hearing in Drosophila depends on the transduction of antennal vibration into receptor potentials by ciliated sensory neurons in Johnston's organ, the antennal chordotonal organ. We previously found that a Drosophila protein in the vanilloid receptor subfamily (TRPV) channel subunit, Nanchung (NAN), is localized to the chordotonal cilia and required to generate sound-evoked potentials (Kim et al., 2003). Here, we show that the only other Drosophila TRPV protein is mutated in the behavioral mutant inactive (iav). The IAV protein forms a hypotonically activated channel when expressed in cultured cells; in flies, it is specifically expressed in the chordotonal neurons, localized to their cilia and required for hearing. IAV and NAN are each undetectable in cilia of mutants lacking the other protein, indicating that they both contribute to a heteromultimeric transduction channel in vivo. A functional green fluorescence protein - IAV fusion protein shows that the channel is restricted to the proximal cilium, constraining models for channel activation.
引用
收藏
页码:9059 / 9066
页数:8
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