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。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fly Pub Date : 2017-10-02 Epub Date: 2017-06-23 DOI:10.1080/19336934.2017.1344374
Jia Wern Pan, Joi McLaughlin, Haining Yang, Charles Leo, Paula Rambarat, Sumie Okuwa, Anaïs Monroy-Eklund, Sabrina Clark, Corbin D Jones, Pelin Cayirlioglu Volkan
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引用次数: 4

摘要

二氧化碳对许多昆虫来说是一个重要的环境信号,调节着许多行为,包括一些对人类有直接影响的行为。为了进一步了解这一系统在密切相关的昆虫物种之间的差异,我们研究了果蝇对二氧化碳的行为反应以及嗅觉系统中二氧化碳感觉神经元的关键发育调节因子的转录谱。我们发现,在我们研究的大多数果蝇中,二氧化碳通常会引起排斥行为,但这种行为在一些谱系中已经消失或减少。这些物种的发育和成虫触角的转录谱比较表明,某些物种的行为差异可能是由于CO2共受体Gr63a的表达差异。此外,Gr63a表达的这些差异与已知参与CO2回路发育的几个基因的表达变化有关,这些基因包括dac和mip120。dac是感受器命运的重要调节剂,感受器含有CO2 orn; mip120是MMB/dREAM表观遗传调控复合体的成员,负责调节CO2受体的表达。相比之下,大多数其他已知的果蝇二氧化碳嗅觉系统的结构、分子和发育成分似乎在所有被研究的谱系中都保存得很好。这些发现表明,二氧化碳感觉ORN发育的某些成分可能在进化上更不稳定,并可能导致物种间二氧化碳诱发行为反应的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative analysis of behavioral and transcriptional variation underlying CO<sub>2</sub> sensory neuron function and development in Drosophila.

Comparative analysis of behavioral and transcriptional variation underlying CO<sub>2</sub> sensory neuron function and development in Drosophila.

Comparative analysis of behavioral and transcriptional variation underlying CO<sub>2</sub> sensory neuron function and development in Drosophila.

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.

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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
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.
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