scholarly journals IDENTIFICATION OF BRAIN SITES CONTROLLING FEMALE RECEPTIVITY IN MOSAICS OF DROSOPHILA MELANOGASTER

Genetics ◽  
1983 ◽  
Vol 103 (2) ◽  
pp. 179-195
Author(s):  
Laurie Tompkins ◽  
Jeffrey C Hall
Keyword(s):  
Drosophila Melanogaster ◽  
Minimum Amount ◽  
Male Courtship ◽  
Experimental Conditions ◽  
Female Receptivity ◽  
Female Genotype ◽  
Courtship Behaviors ◽  
Necessary And Sufficient ◽  
The Brain ◽  
Male Genotype

ABSTRACT We have identified cells in the brain of Drosophila melanogaster that are required to be of female genotype for receptivity to copulation with males. To do this, we determined experimental conditions in which female flies virtually always copulate, then measured the minimum amount of male courtship that is required to stimulate females to indicate their receptivity to copulation. We then observed gynandromorphs with female genitalia to determine whether the sex mosaics elicited at least the minimum amount of courtship and, if so, whether they copulated. By analyzing these gynandromorphs, in which the genotype of external and internal tissues could be ascertained, we were able to identify a group of cells in the dorsal anterior brain that, when bilaterally female, is necessary and sufficient for receptivity to copulation. This group of cells is anatomically distinct from those that are required to be of male genotype for the performance of courtship behaviors.

scholarly journals STUDIES OF ESTERASE 6 IN DROSOPHILA MELANOGASTER. VI. EJACULATE COMPETITIVE ABILITIES OF MALES HAVING NULL OR ACTIVE ALLELES

Genetics ◽  
1981 ◽  
Vol 97 (1) ◽  
pp. 85-94 ◽  
Author(s):  
Donald G Gilbert ◽  
Rollin C Richmond
Keyword(s):  
Drosophila Melanogaster ◽  
Sexual Selection ◽  
Competitive Ability ◽  
Seminal Fluid ◽  
Experimental Conditions ◽  
Competition Mechanism ◽  
Esterase 6 ◽  
Significant Difference ◽  
Female Genotype ◽  
Male Genotype

ABSTRACT Recent studies of the function of the polymorphic seminal fluid enzyme, esterase 6, of Drosophila melanogaster suggested that it may act in the process of sperm displacement (Gilbert, Richmond and Sheehan, 1981a). This report examines the competitive ability of ejaculates from males homozygous for null or active alleles of esterase 6 under three experimental conditions that model aspects of sexual selection affecting males. The results demonstrate no significant difference in ejaculate competition between esterase 6 null or active male types, but marker males used for paternity identification had poorly competitive ejaculates. The proportion of second-male progeny, P  2, used as an index of competition is primarily influenced by second-male genotype and uninfluenced by female genotype. P2 can change with time from remating and be unaffected by different intensities of competition, which suggests a complex ejaculate competition mechanism.

scholarly journals Transcriptome Analysis of NPFR Neurons Reveals a Connection Between proteome Diversity and Social Behavior

2020 ◽  
Author(s):  
Julia Ryvkin ◽  
Assa Bentzur ◽  
Anat Shmueli ◽  
Miriam Tannenbaum ◽  
Omri Shallom ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Social Behavior ◽  
Transcriptome Analysis ◽  
Molecular Signature ◽  
Transcription Profile ◽  
Male Courtship ◽  
Transcriptome Profile ◽  
Protein Ubiquitination ◽  
Spatiotemporal Regulation ◽  
The Brain

AbstractComplex social behaviors are mediated by the activity of highly intricate neuronal networks, the function of which is shaped by their transcriptomic and proteomic content. Contemporary advances in neurogenetics, genomics, and tools for automated behavior analysis make it possible to functionally connect the transcriptome profile of candidate neurons to their role in regulating behavior. In this study we used Drosophila melanogaster to explore the molecular signature of neurons expressing receptor for neuropeptide F (NPF), the fly homologue of neuropeptide Y (NPY). By comparing the transcription profile of NPFR neurons to those of nine other populations of neurons, we discovered that NPFR neurons exhibit a unique transcriptome, enriched with receptors for various neuropeptides and neuromodulators, as well as with genes known to regulate behavioral processes, such as learning and memory. By manipulating RNA editing and protein ubiquitination programs specifically in NPFR neurons, we demonstrate that their delicate transcriptome and proteome repertoires are required to suppress male courtship and certain features of social group interaction. Our results highlight the importance of transcriptome and proteome diversity in the regulation of complex behaviors and pave the path for future dissection of the spatiotemporal regulation of genes within highly complex tissues, such as the brain.

scholarly journals Post-mating Refractoriness in Drosophila melanogaster Depends Upon Ecdysis Triggering Hormone Signaling

2021 ◽  
Author(s):  
Matthew R Meiselman ◽  
Michael E. Adams ◽  
Anindya Ganguly ◽  
Anupama Dahanukar
Keyword(s):  
Drosophila Melanogaster ◽  
Courtship Behavior ◽  
Corpus Allatum ◽  
Hormone Signaling ◽  
Male Courtship ◽  
Hormone Analog ◽  
Sensory Modalities ◽  
Courtship Behaviors ◽  
Ecdysis Triggering Hormone ◽  
Male Courtship Behavior

The decision to engage in courtship depends on external cues from potential mates and internal cues related to maturation, health, and experience. Hormones allow such information to be conveyed to distal tissues in a coordinated fashion. Here, we show Ecdysis-Triggering Hormone (ETH) is a regulator of male courtship in Drosophila melanogaster, and critical for mate choice and courtship inhibition after the completion of copulation. Preventing ETH release increases male-male courtship and decreases post-copulation courtship inhibition (PCCI). Such aberrant male courtship behavior in ETH-deficient males appears to be the consequence of inabilityto integrate pheromone cues into decision making. Silencing of ETH receptor (ETHR) in GR32A-expressing neurons leads to reduced ligand sensitivity and elevated male-male courtship. We find OR67D is critical for suppression of courtship after mating, and ETHR silencing in OR67D-expressing neurons, and GR32A-expressing neurons to a lesser degree, elevates post-copulation courtship. Finally, ETHR silencing in the corpus allatum increases post-copulation courtship; treatment of with juvenile hormone analog partially restores normal post-mating behavior. ETH, a stress-sensitive reproductive hormone, appears to coordinate multiple sensory modalities to guide Drosophila male courtship behaviors, especially after mating.

Effets de deux mutations neurologiques, minibrain3 et no-bridgeKS49, sur la parade nuptiale chez Drosophila melanogaster

1993 ◽  
Vol 71 (5) ◽  
pp. 985-990 ◽  
Author(s):  
A. Bouhouche ◽  
T. Benziane ◽  
G. Vaysse
Keyword(s):  
Drosophila Melanogaster ◽  
Sequential Analysis ◽  
Low Frequency ◽  
Male Courtship ◽  
Protocerebral Bridge ◽  
Copulation Attempt ◽  
The Brain

Male courtship events of two neurological mutants (nobridgeKS49 (nob) and minibrain3 (mnb)) of Drosophila melanogaster were recorded and subjected to quantitative and sequential analysis. The nob mutation, which disorganizes the protocerebral bridge, causes specific defects in courtship: a low frequency of the copulation attempt and the disappearance of the licking – copulation attempt sequence. Thus, the nob males were unable to copulate with receptive females within the 30-min observation. We think that this may be due to an abnormality in their wing vibrations. The mnb mutant, characterized by a reduction of the brain (by more than 50%), exhibited difficulties in initiating courtship and in maintaining contact with the female during courtship. These courtship defects may be due to visual and locomotor anomalies.

scholarly journals Changes in splicing and neuromodulatory gene expression programs in sensory neurons with pheromone signaling and social experience

2021 ◽  
Author(s):  
Pelin C Volkan ◽  
Bryson Deanhardt ◽  
Qichen Duan ◽  
Chengcheng Du ◽  
Charles Soeder ◽  
...  
Keyword(s):  
Sensory Neurons ◽  
Molecular Mechanisms ◽  
Social Experience ◽  
Rna Seq ◽  
Male Courtship ◽  
Wild Type ◽  
Pheromone Signaling ◽  
Courtship Behaviors ◽  
Necessary And Sufficient ◽  
Splicing Patterns

Social experience and pheromone signaling in ORNs affect pheromone responses and male courtship behaviors in Drosophila, however, the molecular mechanisms underlying this circuit-level neuromodulation remain less clear. Previous studies identified social experience and pheromone signaling-dependent modulation of chromatin around behavioral switch gene fruitless, which encodes a transcription factor necessary and sufficient for male behaviors. To identify the molecular mechanisms driving social experience-dependent neuromodulation, we performed RNA-seq from antennal samples of mutant fruit flies in pheromone receptors and fruitless, as well as grouped or isolated wild-type males. We found that loss of pheromone detection differentially alters the levels of fruitless exons suggesting changes in splicing patterns. In addition, many Fruitless target neuromodulatory genes, such as neurotransmitter receptors, ion channels, and ion transporters, are differentially regulated by social context and pheromone signaling. Our results suggest that modulation of circuit activity and behaviors in response to social experience and pheromone signaling arise due to changes in transcriptional programs for neuromodulators downstream of behavioral switch gene function.

scholarly journals Transcriptome Analysis of NPFR Neurons Reveals a Connection Between Proteome Diversity and Social Behavior

2021 ◽  
Vol 15 ◽  
Author(s):  
Julia Ryvkin ◽  
Assa Bentzur ◽  
Anat Shmueli ◽  
Miriam Tannenbaum ◽  
Omri Shallom ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
Social Behavior ◽  
Transcriptome Analysis ◽  
Molecular Signature ◽  
Transcription Profile ◽  
Male Courtship ◽  
Transcriptome Profile ◽  
Protein Ubiquitination ◽  
Spatiotemporal Regulation ◽  
The Brain

Social behaviors are mediated by the activity of highly complex neuronal networks, the function of which is shaped by their transcriptomic and proteomic content. Contemporary advances in neurogenetics, genomics, and tools for automated behavior analysis make it possible to functionally connect the transcriptome profile of candidate neurons to their role in regulating behavior. In this study we used Drosophila melanogaster to explore the molecular signature of neurons expressing receptor for neuropeptide F (NPF), the fly homolog of neuropeptide Y (NPY). By comparing the transcription profile of NPFR neurons to those of nine other populations of neurons, we discovered that NPFR neurons exhibit a unique transcriptome, enriched with receptors for various neuropeptides and neuromodulators, as well as with genes known to regulate behavioral processes, such as learning and memory. By manipulating RNA editing and protein ubiquitination programs specifically in NPFR neurons, we demonstrate that the proper expression of their unique transcriptome and proteome is required to suppress male courtship and certain features of social group interaction. Our results highlight the importance of transcriptome and proteome diversity in the regulation of complex behaviors and pave the path for future dissection of the spatiotemporal regulation of genes within highly complex tissues, such as the brain.

Effect of combined citicoline and glutamate antibodies on acute, generalized convusions induced by pentylenetetrazole in mice

2018 ◽  
pp. 24-29
Author(s):  
М.Н. Карпова ◽  
Л.В. Кузнецова ◽  
Н.Ю. Клишина ◽  
Л.А. Ветрилэ
Keyword(s):  
Drug Combination ◽  
Subcutaneous Injection ◽  
Seizure Activity ◽  
Experimental Conditions ◽  
Slow Progression ◽  
Experiment Control ◽  
Effective Doses ◽  
Experimental Justification ◽  
Series Of Experiments ◽  
The Brain

Цель исследования. На 2 моделях острых генерализованных судорог (ОГС), вызванных конвульсантом пентилентетразолом (ПТЗ), изучить эффективность сочетанного применения ноотропа цитиколина - препарата с противосудорожным действием, нейрорегенеративной, нейропротекторной активностью и антител (АТ) к глутамату, обладающих противосудорожной активностью. Методика. Эксперименты выполнены на мышах-самцах линии C57Bl/6 (n = 87) массой 22-28 г. Эффективность сочетанного применения цитиколина и АТ к глутамату изучали на двух моделях ОГС. Выполнено 2 серии экспериментов. В 1-й серии ОГС вызывали внутривенным введением 1% раствора ПТЗ со скоростью 0,01 мл/с. Для изучения эффективности сочетанного применения препаратов определяли минимальное противосудорожное действие цитиколина (Цераксон, «Nicomed Ferrer Internaсional, S.A.») и АТ к глутамату при их внутрибрюшинном введении. С этой целью цитиколин вводили в дозах 500 и 300 мг/кг за 1 ч до введения ПТЗ, АТ к глутамату - в дозах 5 и 2,5 мг/кг за 1 ч 30 мин до введения ПТЗ. АТ к глутамату получали путем гипериммунизации кроликов соответствующим конъюгированным антигеном. Во 2-й серии ОГС вызывали подкожным введением ПТЗ в дозе 85 мг/кг. Для изучения эффективности сочетанного действия изучаемых препаратов последние вводили в минимально действующих дозах, установленных в 1-й серии экспериментов. Контролем во всех сериях опытов служили животные, которым вводили в аналогичных условиях и в том же объеме физиологический раствор. Результаты. Показано, что сочетанное применение цитиколина и АТ к глутамату в минимально действующих дозах (300 и 2,5 мг/кг соответственно) при моделировании ОГС не вызывало повышения судорожной активности мозга и усиления противосудорожных свойств препаратов. Заключение. Cочетанное применение цитиколина и АТ к глутамату в минимально действующих дозах не вызывало повышения судорожной активности мозга, что свидетельствует о безопасности совместного применения препаратов. Проведенное исследование может служить также экспериментальным обоснованием возможности использования сочетанного применения данных препаратов при судорогах с целью замедления прогрессирования нейродегенеративных процессов и благоприятного влияния на когнитивные функции. Aim. To study the effectivity of a combination of citicoline, a nootropic substance with neuroregenerative, neuroprotective, and anticonvulsant actions, and glutamate antibodies (АB) with an anticonvulsant action in two models of acute generalized convulsions (AGC) caused by the convulsant pentylenetetrazole (PTZ). Methods. Experiments were conducted on C57Bl/6 mice (n = 87) weighing 22-28 g. Effects of combined citicoline and glutamate АB were studied on two models of AGС. In the first series of experiments, AGС was induced by intravenous infusion of a 1% PTZ solution at 0.01 ml/sec. In the second series, AGС was induced by a subcutaneous injection of PTZ 85 mg/kg. To evaluate efficacy of the drug combination minimum intraperitoneal anticonvulsant doses of citicoline (Tserakson, Nicomed Ferrer Internacional, S.A.) and glutamate АB were determined. To this purpose, citicoline was administered at 500 and 300 mg/kg 1 h prior to PTZ, and glutamate АB was administered at 5 and 2.5 mg/kg 90 min prior to PTZ. Glutamate АB was obtained by hyperimmunization of rabbits with a respective conjugated antigen. In the second series of experiments, AGС was induced by a subcutaneous injection of PTZ 85 mg/kg. To evaluate the effect of the drug combination, the drugs were administered at the minimum effective doses determined in the first series of experiment. Control animals were injected with the same volume of saline in the same experimental conditions. Results. The combination of citicoline and glutamate AB used at minimum effective doses of 300 and 2.5 mg/kg, respectively, did not increase the seizure activity in the brain and enhanced anticonvulsant properties of the drugs in two models of AGС. Conclusion. The combination of citicoline and glutamate AT at minimum effective doses did not increase the convulsive activity in the brain, which supported safety of the drug combination. Besides, this study can serve as an experimental justification for using the drug combination in convulsions to favorably influence cognitive functions and slow progression of neurodegenerative processes.

scholarly journals Correction: The Nutrient-Responsive Hormone CCHamide-2 Controls Growth by Regulating Insulin-like Peptides in the Brain of Drosophila melanogaster

PLoS Genetics ◽  
2015 ◽  
Vol 11 (9) ◽  
pp. e1005481 ◽  
Author(s):  
Hiroko Sano ◽  
Akira Nakamura ◽  
Michael J. Texada ◽  
James W. Truman ◽  
Hiroshi Ishimoto ◽  
...  
Keyword(s):  
Drosophila Melanogaster ◽  
The Brain

Regional blood flow in the brain and spinal cord of hypothermic rats

1989 ◽  
Vol 257 (3) ◽  
pp. H785-H790
Author(s):  
T. Sakamoto ◽  
W. W. Monafo
Keyword(s):  
Spinal Cord ◽  
Blood Flow ◽  
Brain Stem ◽  
Regional Blood Flow ◽  
Experimental Conditions ◽  
Pentobarbital Sodium ◽  
Arterial Blood ◽  
Group A ◽  
Group B ◽  
The Brain

[14C]butanol tissue uptake was used to measure simultaneously regional blood flow in three regions of the brain (cerebral and cerebellar hemispheres and brain stem) and in five levels of the spinal cord in 10 normothermic rats (group A) and in 10 rats in which rectal temperature had been lowered to 27.7 +/- 0.3 degrees C by applying ice to the torso (group B). Pentobarbital sodium anesthesia was used. Mean arterial blood pressure varied minimally between groups as did arterial pH, PO2, and PCO2. In group A, regional spinal cord blood flow (rSCBF) varied from 49.7 +/- 1.6 to 62.6 +/- 2.1 ml.min-1.100 g-1; in brain, regional blood flow (rBBF) averaged 74.4 +/- 2.3 ml.min-1.100 g-1 in the whole brain and was highest in the brain stem. rSCBF in group B was elevated in all levels of the cord by 21-34% (P less than 0.05). rBBF, however, was lowered by 21% in the cerebral hemispheres (P less than 0.001) and by 14% in the brain as a whole (P less than 0.05). The changes in calculated vascular resistance tended to be inversely related to blood flow in all tissues. We conclude that rBBF is depressed in acutely hypothermic pentobarbital sodium-anesthetized rats, as has been noted before, but that rSCBF rises under these experimental conditions. The elevation of rSCBF in hypothermic rats confirms our previous observations.

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