scholarly journals Neuropeptide F regulates courtship in Drosophila through a male-specific neuronal circuit

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Weiwei Liu ◽  
Anindya Ganguly ◽  
Jia Huang ◽  
Yijin Wang ◽  
Jinfei D Ni ◽  
...  

Male courtship is provoked by perception of a potential mate. In addition, the likelihood and intensity of courtship are influenced by recent mating experience, which affects sexual drive. Using Drosophila melanogaster, we found that the homolog of mammalian neuropeptide Y, neuropeptide F (NPF), and a cluster of male-specific NPF (NPFM) neurons, regulate courtship through affecting courtship drive. Disrupting NPF signaling produces sexually hyperactive males, which are resistant to sexual satiation, and whose courtship is triggered by sub-optimal stimuli. We found that NPFM neurons make synaptic connections with P1 neurons, which comprise the courtship decision center. Activation of P1 neurons elevates NPFM neuronal activity, which then act through NPF receptor neurons to suppress male courtship, and maintain the proper level of male courtship drive.

1988 ◽  
Vol 51 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Jean-Marc Jallon ◽  
Ginette Lauge ◽  
Luc Orssaud ◽  
Claude Antony

SummaryXY and XX doublesex D. melanogaster, expressing variable intersexual phenotypes, were compared for their pheromone levels (e.g. 7, 11-heptacosadiene, the main excitatory pheromone of females, and vaccenyl acetate, an inhibitory compound produced only by males). Despite the intersexual phenotype and the presence of female traits, the pheromone patterns of the homozygous dsx mutants, XY as well as XX, were similar to those of heterozygous males. Female-specific dienes were never found in significant amounts in such flies, which often showed significant amounts of the male-specific acetate and triggered very reduced levels of male courtship wing vibration.


2019 ◽  
Author(s):  
Weiwei Liu ◽  
Anindya Ganguly ◽  
Jia Huang ◽  
Yijin Wang ◽  
Jinfei D Ni ◽  
...  

Development ◽  
2001 ◽  
Vol 128 (19) ◽  
pp. 3809-3817 ◽  
Author(s):  
Silvia Bongiorni ◽  
Milena Mazzuoli ◽  
Stefania Masci ◽  
Giorgio Prantera

The behavior of chromosomes during development of the mealybug Planococcus citri provides one of the most dramatic examples of facultative heterochromatization. In male embryos, the entire haploid paternal chromosome set becomes heterochromatic at mid-cleavage. Male mealybugs are thus functionally haploid, owing to heterochromatization (parahaploidy). To understand the mechanisms underlying facultative heterochromatization in male mealybugs, we have investigated the possible involvement of an HP-1-like protein in this process. HP-1 is a conserved, nonhistone chromosomal protein with a proposed role in heterochromatinization in other species. It was first identified in Drosophila melanogaster as a protein enriched in the constitutive heterochromatin of polytene chromosome. Using a monoclonal antibody raised against the Drosophila HP-1 in immunoblot and immunocytological experiments, we provide evidence for the presence of an HP-1-like in Planococcus citri males and females. In males, the HP-1-like protein is preferentially associated with the male-specific heterochromatin. In the developing male embryos, its appearance precedes the onset of heterochromatization. In females, the HP-1-like protein displays a scattered but reproducible localization pattern along chromosomes. The results indicate a role for an HP-1-like protein in the facultative heterochromatization process.


2012 ◽  
Vol 520 (5) ◽  
pp. 970-987 ◽  
Author(s):  
Christiane Hermann ◽  
Taishi Yoshii ◽  
Verena Dusik ◽  
Charlotte Helfrich-Förster

PLoS ONE ◽  
2011 ◽  
Vol 6 (4) ◽  
pp. e18853 ◽  
Author(s):  
Ying Chen ◽  
Hongzheng Dai ◽  
Sidi Chen ◽  
Luoying Zhang ◽  
Manyuan Long

2020 ◽  
Author(s):  
Jun Tomita ◽  
Gosuke Ban ◽  
Yoshiaki S. Kato ◽  
Kazuhiko Kume

AbstractThe central complex is one of the major brain regions that control sleep in Drosophila, but the circuitry details of sleep regulation have yet to be elucidated. Here, we show a novel sleep-regulating neuronal circuit in the protocerebral bridge (PB) of the central complex. Activation of the PB interneurons labeled by the R59E08-Gal4 and the PB columnar neurons in the R52B10-Gal4 promoted sleep and wakefulness, respectively. A targeted GFP reconstitution across synaptic partners (t-GRASP) analysis demonstrated synaptic contacts between these two groups of sleep-regulating PB neurons. Furthermore, we found that activation of a pair of dopaminergic (DA) neurons projecting to the PB (T1 DA neurons) decreased sleep. The wake-promoting T1 DA neurons and the sleep-promoting PB interneurons formed close associations. Dopamine 2-like receptor (Dop2R) knockdown in the sleep-promoting PB interneurons increased sleep. These results indicated that the neuronal circuit in the PB regulated by dopamine signaling mediates sleep-wakefulness.


1991 ◽  
Vol 10 (1) ◽  
pp. 163-169 ◽  
Author(s):  
C. Samakovlis ◽  
P. Kylsten ◽  
D. A. Kimbrell ◽  
A. Engström ◽  
D. Hultmark

Sign in / Sign up

Export Citation Format

Share Document