4.7 Article

Projections of Drosophila multidendritic neurons in the central nervous system: links with peripheral dendrite morphology

期刊

DEVELOPMENT
卷 134, 期 1, 页码 55-64

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.02666

关键词

Drosophila; sensory map; dendritic arborization neurons; genetic screen; axon targeting; dendrite morphogenesis

资金

  1. NIMH NIH HHS [K99 MH080599, K99 MH080599-01, K99 MH080599-02] Funding Source: Medline
  2. NINDS NIH HHS [F32 NS43027, R01 NS 40929, F32 NS46847] Funding Source: Medline
  3. NATIONAL INSTITUTE OF MENTAL HEALTH [K99MH080599] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS040929, F32NS046847, F32NS043027] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Neurons establish diverse dendritic morphologies during development, and a major challenge is to understand how these distinct developmental programs might relate to, and influence, neuronal function. Drosophila dendritic arborization (da) sensory neurons display class-specific dendritic morphology with extensive coverage of the body wall. To begin to build a basis for linking dendrite structure and function in this genetic system, we analyzed da neuron axon projections in embryonic and larval stages. We found that multiple parameters of axon morphology, including dorsoventral position, midline crossing and collateral branching, correlate with dendritic morphological class. We have identified a class-specific medial-lateral layering of axons in the central nervous system formed during embryonic development, which could allow different classes of da neurons to develop differential connectivity to second-order neurons. We have examined the effect of Robo family members on class-specific axon lamination, and have also taken a forward genetic approach to identify new genes involved in axon and dendrite development. For the latter, we screened the third chromosome at high resolution in vivo for mutations that affect class IV da neuron morphology. Several known loci, as well as putative novel mutations, were identified that contribute to sensory dendrite and/or axon patterning. This collection of mutants, together with anatomical data on dendrites and axons, should begin to permit studies of dendrite diversity in a combined developmental and functional context, and also provide a foundation for understanding shared and distinct mechanisms that control axon and dendrite morphology.

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