尖端技术揭示了果蝇神经系统神经发生的时间调节

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Fly Pub Date : 2022-05-13 DOI:10.1080/19336934.2022.2073158
Makoto Sato, Takumi Suzuki
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引用次数: 1

摘要

在中枢神经系统(central nervous system, CNS)的发育过程中,有规律地产生大量神经元,形成精确的神经回路。在这一过程中,神经祖细胞由于其内在的基因调控机制和外在的机制,随着时间的推移产生不同的神经元。果蝇中枢神经系统在阐明控制神经发生的时间机制方面发挥了重要作用。研究表明,在胚胎中枢神经系统中,一系列时间转录因子在神经祖细胞中有序表达,并调节神经元的时间特异性。此外,在幼虫中枢神经系统发育中的视叶和中央脑中也发现了类似的机制。然而,仅通过分子遗传学方法很难阐明许多不同细胞类型中许多分子的功能。近年来,利用单细胞RNA-seq等方法进行组学分析已被用于果蝇神经系统的大规模研究,为理解神经发生的时间机制做出了重要贡献。本文将对神经发生的时间模式的最新研究成果和前沿技术的贡献进行综述。
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Cutting edge technologies expose the temporal regulation of neurogenesis in the Drosophila nervous system
ABSTRACT During the development of the central nervous system (CNS), extremely large numbers of neurons are produced in a regular fashion to form precise neural circuits. During this process, neural progenitor cells produce different neurons over time due to their intrinsic gene regulatory mechanisms as well as extrinsic mechanisms. The Drosophila CNS has played an important role in elucidating the temporal mechanisms that control neurogenesis over time. It has been shown that a series of temporal transcription factors are sequentially expressed in neural progenitor cells and regulate the temporal specification of neurons in the embryonic CNS. Additionally, similar mechanisms are found in the developing optic lobe and central brain in the larval CNS. However, it is difficult to elucidate the function of numerous molecules in many different cell types solely by molecular genetic approaches. Recently, omics analysis using single-cell RNA-seq and other methods has been used to study the Drosophila nervous system on a large scale and is making a significant contribution to the understanding of the temporal mechanisms of neurogenesis. In this article, recent findings on the temporal patterning of neurogenesis and the contributions of cutting-edge technologies will be reviewed.
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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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