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  Visual projection neurons mediating directed courtship in Drosophila

Ribeiro, I. M. A., Drews, M., Bahl, A., Machacek, C., Borst, A., & Dickson, B. J. (2018). Visual projection neurons mediating directed courtship in Drosophila. Cell, 174(3), 607-621.e18. doi:10.1016/j.cell.2018.06.020.

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Ribeiro, Ines M. A.1, Autor           
Drews, Michael1, Autor           
Bahl, Armin1, Autor           
Machacek, Christian, Autor
Borst, Alexander1, Autor           
Dickson, Barry J., Autor
Affiliations:
1Department: Circuits-Computation-Models / Borst, MPI of Neurobiology, Max Planck Society, ou_1113548              

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Schlagwörter: RETINAL GANGLION-CELLS; GENETIC FEMINIZATION; OPTOGENETIC CONTROL; LARVAL ZEBRAFISH; NEURAL CIRCUIT; MOTION VISION; PREY CAPTURE; BEHAVIOR; MELANOGASTER; FLYBiochemistry & Molecular Biology; Cell Biology;
 Zusammenfassung: Many animals rely on vision to detect, locate, and track moving objects. In Drosophila courtship, males primarily use visual cues to orient toward and follow females and to select the ipsilateral wing for courtship song. Here, we show that the LC10 visual projection neurons convey essential visual information during courtship. Males with LC10 neurons silenced are unable to orient toward or maintain proximity to the female and do not predominantly use the ipsilateral wing when singing. LC10 neurons preferentially respond to small moving objects using an antagonistic motion-based center-surround mechanism. Unilateral activation of LC10 neurons recapitulates the orienting and ipsilateral wing extension normally elicited by females, and the potency with which LC10 induces wing extension is enhanced in a state of courtship arousal controlled by male-specific P1 neurons. These data suggest that LC10 is a major pathway relaying visual input to the courtship circuits in the male brain.

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Sprache(n): eng - English
 Datum: 2018-07-26
 Publikationsstatus: Erschienen
 Seiten: 33
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000439870500011
DOI: 10.1016/j.cell.2018.06.020
 Art des Abschluß: -

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Titel: Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 174 (3) Artikelnummer: - Start- / Endseite: 607 - 621.e18 Identifikator: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183