» Articles » PMID: 17360588

Modulation of Drosophila Male Behavioral Choice

Overview
Specialty Science
Date 2007 Mar 16
PMID 17360588
Citations 84
Authors
Affiliations
Soon will be listed here.
Abstract

The reproductive and defensive behaviors that are initiated in response to specific sensory cues can provide insight into how choices are made between different social behaviors. We manipulated both the activity and sex of a subset of neurons and found significant changes in male social behavior. Results from aggression assays indicate that the neuromodulator octopamine (OCT) is necessary for Drosophila males to coordinate sensory cue information presented by a second male and respond with the appropriate behavior: aggression rather than courtship. In competitive male courtship assays, males with no OCT or with low OCT levels do not adapt to changing sensory cues and court both males and females. We identified a small subset of neurons in the suboesophageal ganglion region of the adult male brain that coexpress OCT and male forms of the neural sex determination factor, Fruitless (Fru(M)). A single Fru(M)-positive OCT neuron sends extensive bilateral arborizations to the suboesophageal ganglion, the lateral accessory lobe, and possibly the posterior antennal lobe, suggesting a mechanism for integrating multiple sensory modalities. Furthermore, eliminating the expression of Fru(M) by transformer expression in OCT/tyramine neurons changes the aggression versus courtship response behavior. These results provide insight into how complex social behaviors are coordinated in the nervous system and suggest a role for neuromodulators in the functioning of male-specific circuitry relating to behavioral choice.

Citing Articles

Exploring the versatility of as a model organism in biomedical research: a comprehensive review.

Atoki A, Aja P, Shinkafi T, Ondari E, Adeniyi A, Fasogbon I Fly (Austin). 2024; 19(1):2420453.

PMID: 39722550 PMC: 11702942. DOI: 10.1080/19336934.2024.2420453.


NMDAR-CaMKII Pathway as a Central Regulator of Aggressiveness: Evidence from Transcriptomic and Metabolomic Analysis in Swimming Crabs .

Liang Q, Liu D, Zhu B, Wang F Int J Mol Sci. 2024; 25(23).

PMID: 39684272 PMC: 11640798. DOI: 10.3390/ijms252312560.


Neurons Underlying Aggression-Like Actions That Are Shared by Both Males and Females in .

Tao L, Ayambem D, Barranca V, Bhandawat V J Neurosci. 2024; 44(44).

PMID: 39317475 PMC: 11529818. DOI: 10.1523/JNEUROSCI.0142-24.2024.


Octopamine is required for successful reproduction in the classical insect model, Rhodnius prolixus.

Leyria J, Orchard I, Lange A PLoS One. 2024; 19(7):e0306611.

PMID: 38995904 PMC: 11244822. DOI: 10.1371/journal.pone.0306611.


Octopaminergic descending neurons in : Connectivity, tonic activity and relation to locomotion.

Babski H, Codianni M, Bhandawat V Heliyon. 2024; 10(9):e29952.

PMID: 38698992 PMC: 11064449. DOI: 10.1016/j.heliyon.2024.e29952.


References
1.
Coyne J, Crittenden A, Mah K . Genetics of a pheromonal difference contributing to reproductive isolation in Drosophila. Science. 1994; 265(5177):1461-4. DOI: 10.1126/science.8073292. View

2.
Cahill L . Why sex matters for neuroscience. Nat Rev Neurosci. 2006; 7(6):477-84. DOI: 10.1038/nrn1909. View

3.
Monastirioti M, Linn Jr C, White K . Characterization of Drosophila tyramine beta-hydroxylase gene and isolation of mutant flies lacking octopamine. J Neurosci. 1996; 16(12):3900-11. PMC: 6578608. View

4.
Manoli D, Baker B . Median bundle neurons coordinate behaviours during Drosophila male courtship. Nature. 2004; 430(6999):564-9. DOI: 10.1038/nature02713. View

5.
Hasselmo M . Neuromodulation and cortical function: modeling the physiological basis of behavior. Behav Brain Res. 1995; 67(1):1-27. DOI: 10.1016/0166-4328(94)00113-t. View