刺激和抑制g蛋白信号传递驱动cAMP积累,促进脊索动物及时变态。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-06-18 DOI:10.7554/eLife.99825
Akiko Hozumi, Nozomu M Totsuka, Arata Onodera, Yanbin Wang, Mayuko Hamada, Akira Shiraishi, Honoo Satake, Takeo Horie, Kohji Hotta, Yasunori Sasakura
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引用次数: 0

摘要

海鞘的幼虫在通过其粘附器官粘附到基质上数十分钟后开始变形。建议在附着与变形起始之间留有间隙,以保证附着的刚性,使乔娜在变形失去机车活动后仍能保持沉降。产生间隙的机制尚不清楚。在这里,通过结合基因功能分析、药理学分析和实时成像,我们提出这个间隙代表了足够的环磷酸腺苷(cAMP)积累触发变态所需的时间。在已知的神经递质GABA的下游信号级联中,不仅有Gs通路,还有Gi和Gq通路参与了乔纳变态的启动。刺激性和抑制性g蛋白的相互串扰是cAMP产生的加速器和制动器,确保在适当的时间和适当的情况下忠实地开始变态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stimulatory and inhibitory G-protein signaling relays drive cAMP accumulation for timely metamorphosis in the chordate Ciona.

Larvae of the ascidian Ciona initiate metamorphosis tens of minutes after adhesion to a substratum via their adhesive organ. The gap between adhesion and metamorphosis initiation is suggested to ensure the rigidity of adhesion, allowing Ciona to maintain settlement after losing locomotive activity through metamorphosis. The mechanism producing the gap is unknown. Here, by combining gene functional analyses, pharmacological analyses, and live imaging, we propose that the gap represents the time required for sufficient cyclic adenosine monophosphate (cAMP) accumulation to trigger metamorphosis. Not only the Gs pathway but also the Gi and Gq pathways are involved in the initiation of metamorphosis in the downstream signaling cascade of the neurotransmitter GABA, the known initiator of Ciona metamorphosis. The mutual crosstalk of stimulatory and inhibitory G-proteins functions as the accelerator and brake for cAMP production, ensuring the faithful initiation of metamorphosis at an appropriate time and in the right situation.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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