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Diamandi, J. A.

Publications and source records attributed to Diamandi, J. A..

2 recordsLinked to original sources

Cis-regulatory fragments from the dissatisfaction gene identify novel mating behavior neurons in female Drosophila

During Drosophila courtship, males chase and sing to females, while females perform abdominal behaviors to indicate their willingness to mate. The nerve cord circuits in females that produce their abdominal behaviors are poorly characterized. We recently identified an anatomically diverse population of abdominal interneurons, the DDAG neurons, which express the Tlx-like nuclear receptor dissatisfaction (dsf) and influence several female mating behaviors. Here, we searched the dsf locus for cis-regulatory enhancer fragments that regulate its spatial expression in the adult and larval central nervous system. We found several enhancers, most located within two introns, that drove reporter expression in subsets of dsf-expressing neurons throughout the brain and nerve cord. Using one of these enhancers, we genetically isolated a single subtype of female-specific DDAG local interneurons. Optogenetic activation of these neurons triggered vaginal plate opening in both unmated and mated females, a behavior used by Drosophila females to signal receptivity to courting males. Our findings offer new reagents to target dsf-expressing cells and new insights into the neural substrates in Drosophila females that express their mating decisions during courtship.

neuroscience↗

Developmental remodeling repurposes larval neurons for sexual behaviors in adult Drosophila

Most larval neurons in Drosophila are repurposed during metamorphosis for functions in adult life, but their contribution to the neural circuits for sexually dimorphic behaviors is unknown. Here, we identify two interneurons in the nerve cord of adult Drosophila females that control ovipositor extrusion, a courtship rejection behavior performed by mated females. We show that these two neurons are present in the nerve cord of larvae as mature, sexually monomorphic interneurons. During pupal development, they acquire the expression of the sexual differentiation gene, doublesex, undergo doublesex-dependent programmed cell death in males, and are remodeled in females for functions in female mating behavior. Our results demonstrate that the neural circuits for courtship in Drosophila are built in part using neurons that are sexually reprogrammed from former sex-shared activities in larval life.

neuroscience↗