Jia Wern Pan, Joi McLaughlin, Haining Yang, Charles Leo, Paula Rambarat, Sumie Okuwa, Anaïs Monroy-Eklund, Sabrina Clark, Corbin D Jones, Pelin Cayirlioglu Volkan
{"title":"果蝇二氧化碳感觉神经元功能和发育的行为和转录变异的比较分析。","authors":"Jia Wern Pan, Joi McLaughlin, Haining Yang, Charles Leo, Paula Rambarat, Sumie Okuwa, Anaïs Monroy-Eklund, Sabrina Clark, Corbin D Jones, Pelin Cayirlioglu Volkan","doi":"10.1080/19336934.2017.1344374","DOIUrl":null,"url":null,"abstract":"<p><p>Carbon dioxide is an important environmental cue for many insects, regulating many behaviors including some that have direct human impacts. To further improve our understanding of how this system varies among closely related insect species, we examined both the behavioral response to CO<sub>2</sub> as well as the transcriptional profile of key developmental regulators of CO<sub>2</sub> sensory neurons in the olfactory system across the Drosophila genus. We found that CO<sub>2</sub> generally evokes repulsive behavior across most of the Drosophilids we examined, but this behavior has been lost or reduced in several lineages. Comparisons of transcriptional profiles from the developing and adult antennae for subset these species suggest that behavioral differences in some species may be due to differences in the expression of the CO<sub>2</sub> co-receptor Gr63a. Furthermore, these differences in Gr63a expression are correlated with changes in the expression of a few genes known to be involved in the development of the CO<sub>2</sub> circuit, namely dac, an important regulator of sensilla fate for sensilla that house CO<sub>2</sub> ORNs, and mip120, a member of the MMB/dREAM epigenetic regulatory complex that regulates CO<sub>2</sub> receptor expression. In contrast, most of the other known structural, molecular, and developmental components of the peripheral Drosophila CO<sub>2</sub> olfactory system seem to be well-conserved across all examined lineages. These findings suggest that certain components of CO<sub>2</sub> sensory ORN development may be more evolutionarily labile, and may contribute to differences in CO<sub>2</sub>-evoked behavioral responses across species.</p>","PeriodicalId":12128,"journal":{"name":"Fly","volume":"11 4","pages":"239-252"},"PeriodicalIF":2.4000,"publicationDate":"2017-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19336934.2017.1344374","citationCount":"4","resultStr":"{\"title\":\"Comparative analysis of behavioral and transcriptional variation underlying CO<sub>2</sub> sensory neuron function and development in Drosophila.\",\"authors\":\"Jia Wern Pan, Joi McLaughlin, Haining Yang, Charles Leo, Paula Rambarat, Sumie Okuwa, Anaïs Monroy-Eklund, Sabrina Clark, Corbin D Jones, Pelin Cayirlioglu Volkan\",\"doi\":\"10.1080/19336934.2017.1344374\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Carbon dioxide is an important environmental cue for many insects, regulating many behaviors including some that have direct human impacts. To further improve our understanding of how this system varies among closely related insect species, we examined both the behavioral response to CO<sub>2</sub> as well as the transcriptional profile of key developmental regulators of CO<sub>2</sub> sensory neurons in the olfactory system across the Drosophila genus. We found that CO<sub>2</sub> generally evokes repulsive behavior across most of the Drosophilids we examined, but this behavior has been lost or reduced in several lineages. Comparisons of transcriptional profiles from the developing and adult antennae for subset these species suggest that behavioral differences in some species may be due to differences in the expression of the CO<sub>2</sub> co-receptor Gr63a. Furthermore, these differences in Gr63a expression are correlated with changes in the expression of a few genes known to be involved in the development of the CO<sub>2</sub> circuit, namely dac, an important regulator of sensilla fate for sensilla that house CO<sub>2</sub> ORNs, and mip120, a member of the MMB/dREAM epigenetic regulatory complex that regulates CO<sub>2</sub> receptor expression. In contrast, most of the other known structural, molecular, and developmental components of the peripheral Drosophila CO<sub>2</sub> olfactory system seem to be well-conserved across all examined lineages. 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Comparative analysis of behavioral and transcriptional variation underlying CO2 sensory neuron function and development in Drosophila.
Carbon dioxide is an important environmental cue for many insects, regulating many behaviors including some that have direct human impacts. To further improve our understanding of how this system varies among closely related insect species, we examined both the behavioral response to CO2 as well as the transcriptional profile of key developmental regulators of CO2 sensory neurons in the olfactory system across the Drosophila genus. We found that CO2 generally evokes repulsive behavior across most of the Drosophilids we examined, but this behavior has been lost or reduced in several lineages. Comparisons of transcriptional profiles from the developing and adult antennae for subset these species suggest that behavioral differences in some species may be due to differences in the expression of the CO2 co-receptor Gr63a. Furthermore, these differences in Gr63a expression are correlated with changes in the expression of a few genes known to be involved in the development of the CO2 circuit, namely dac, an important regulator of sensilla fate for sensilla that house CO2 ORNs, and mip120, a member of the MMB/dREAM epigenetic regulatory complex that regulates CO2 receptor expression. In contrast, most of the other known structural, molecular, and developmental components of the peripheral Drosophila CO2 olfactory system seem to be well-conserved across all examined lineages. These findings suggest that certain components of CO2 sensory ORN development may be more evolutionarily labile, and may contribute to differences in CO2-evoked behavioral responses across species.
期刊介绍:
Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions.
Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.