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  Drosophila Psidin Regulates Olfactory Neuron Number and Axon Targeting through Two Distinct Molecular Mechanisms

Stephan, D., Sanchez-Soriano, N., Loschek, L. F., Gerhards, R., Gutmann, S., Storchova, Z., Prokop, A., & Kadow, I. C. G. (2012). Drosophila Psidin Regulates Olfactory Neuron Number and Axon Targeting through Two Distinct Molecular Mechanisms. JOURNAL OF NEUROSCIENCE, 32(46), 16080-16094. doi:10.1523/JNEUROSCI.3116-12.2012.

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資料種別: 学術論文

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 作成者:
Stephan, Daniel1, 著者           
Sanchez-Soriano, Natalia2, 著者
Loschek, Laura F.1, 著者           
Gerhards, Ramona1, 著者           
Gutmann, Susanne3, 著者           
Storchova, Zuzana3, 著者           
Prokop, Andreas2, 著者
Kadow, Ilona C. Grunwald1, 著者           
所属:
1Max Planck Research Group: Sensory Neurogenetics / Grunwald-Kadow, MPI of Neurobiology, Max Planck Society, ou_1113556              
2external, ou_persistent22              
3Storchova, Zuzana / Maintenance of Genome Stability, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565171              

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キーワード: GROWTH CONE; PROTEINS; GUIDANCE; DYNAMICS; TROPOMYOSIN; MOTILITY; SYSTEM; RHO
 要旨: The formation of neuronal circuits is a key process of development, laying foundations for behavior. The cellular mechanisms regulating circuit development are not fully understood. Here, we reveal Psidin as an intracellular regulator of Drosophila olfactory system formation. We show that Psidin is required in several classes of olfactory receptor neurons (ORNs) for survival and subsequently for axon guidance. During axon guidance, Psidin functions as an actin regulator and antagonist of Tropomyosin. Accordingly, Psidin-deficient primary neurons in culture display growth cones with significantly smaller lamellipodia. This lamellipodial phenotype, as well as the mistargeting defects in vivo, is suppressed by parallel removal of Tropomyosin. In contrast, Psidin functions as the noncatalytic subunit of the N-acetyltransferase complex B (NatB) to maintain the number of ORNs. Psidin physically binds the catalytic NatB subunit CG14222 (dNAA20) and functionally interacts with it in vivo. We define the dNAA20 interaction domain within Psidin and identify a conserved serine as a candidate for phosphorylation-mediated regulation of NatB complex formation. A phosphomimetic mutation of this serine showed severely reduced binding to dNAA20 in vitro. In vivo, it fully rescued the targeting defect but not the reduction in neuron numbers. In addition, we show that a different amino acid point mutation shows exactly the opposite effect by rescuing only the cell number but not the axon targeting defect. Together, our data suggest that Psidin plays two independent developmental roles via the acquisition of separate signaling pathways, both of which contribute to the formation of olfactory circuits.

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言語: eng - English
 日付: 2012-11-14
 出版の状態: 出版
 ページ: 15
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): ISI: 000311091000003
DOI: 10.1523/JNEUROSCI.3116-12.2012
 学位: -

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出版物 1

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出版物名: JOURNAL OF NEUROSCIENCE
種別: 学術雑誌
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出版社, 出版地: 11 DUPONT CIRCLE, NW, STE 500, WASHINGTON, DC 20036 USA : SOC NEUROSCIENCE
ページ: - 巻号: 32 (46) 通巻号: - 開始・終了ページ: 16080 - 16094 識別子(ISBN, ISSN, DOIなど): ISSN: 0270-6474