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1.
Development ; 138(22): 4899-909, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22007130

RESUMEN

A defining characteristic of neuronal cell type is the growth of axons and dendrites into specific layers and columns of the brain. Although differences in cell surface receptors and adhesion molecules are known to cause differences in synaptic specificity, differences in downstream signaling mechanisms that determine cell type-appropriate targeting patterns are unknown. Using a forward genetic screen in Drosophila, we identify the GTPase effector Genghis khan (Gek) as playing a crucial role in the ability of a subset of photoreceptor (R cell) axons to innervate appropriate target columns. In particular, single-cell mosaic analyses demonstrate that R cell growth cones lacking Gek function grow to the appropriate ganglion, but frequently fail to innervate the correct target column. Further studies reveal that R cell axons lacking the activity of the small GTPase Cdc42 display similar defects, providing evidence that these proteins regulate a common set of processes. Gek is expressed in all R cells, and a detailed structure-function analysis reveals a set of regulatory domains with activities that restrict Gek function to the growth cone. Although Gek does not normally regulate layer-specific targeting, ectopic expression of Gek is sufficient to alter the targeting choices made by another R cell type, the targeting of which is normally Gek independent. Thus, specific regulation of cytoskeletal responses to targeting cues is necessary for cell type-appropriate synaptic specificity.


Asunto(s)
Proteínas de Drosophila/fisiología , Drosophila/genética , Ojo/inervación , Proteínas Serina-Treonina Quinasas/fisiología , Visión Ocular/genética , Vías Visuales/fisiología , Animales , Animales Modificados Genéticamente , Axones/metabolismo , Axones/fisiología , Citoesqueleto/metabolismo , Dendritas/metabolismo , Drosophila/crecimiento & desarrollo , Drosophila/fisiología , Proteínas de Drosophila/genética , Estudios de Asociación Genética , Conos de Crecimiento/metabolismo , Conos de Crecimiento/fisiología , Modelos Biológicos , Neuronas Aferentes/metabolismo , Neuronas Aferentes/fisiología , Células Fotorreceptoras de Invertebrados/metabolismo , Células Fotorreceptoras de Invertebrados/fisiología , Proteínas Serina-Treonina Quinasas/genética , Sensibilidad y Especificidad , Transmisión Sináptica/genética , Transmisión Sináptica/fisiología , Vías Visuales/metabolismo
2.
Cell Adh Migr ; 3(1): 36-42, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19372748

RESUMEN

Cell adhesion is the fundamental driving force that establishes complex cellular architectures, with the nervous system offering a striking, sophisticated case study. Developing neurons adhere to neighboring neurons, their synaptic partners, and to glial cells. These adhesive interactions are required in a diverse array of contexts, including cell migration, axon guidance and targeting, as well as synapse formation and physiology. Forward and reverse genetic screens in the fruit fly Drosophila have uncovered several adhesion molecules that are required for neural development, and detailed cell biological analyses are beginning to unravel how these factors shape nervous system connectivity. Here we review our current understanding of the most prominent of these adhesion factors and their modes of action.


Asunto(s)
Moléculas de Adhesión Celular/metabolismo , Drosophila melanogaster/metabolismo , Sistema Nervioso/metabolismo , Animales , Adhesión Celular , Drosophila melanogaster/citología , Sistema Nervioso/citología , Sistema Nervioso/crecimiento & desarrollo , Neuroglía/citología , Neuroglía/metabolismo , Neuronas/citología , Neuronas/metabolismo
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