果蝇光感受器和光传导中视紫红质水平的维持需要蛋白激酶D。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fly Pub Date : 2018-01-01 Epub Date: 2019-02-05 DOI:10.1080/19336934.2019.1565256
Sudipta Ashe, Shweta Yadav
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引用次数: 1

摘要

在果蝇光转导过程中,G蛋白偶联受体(GPCR)视紫红质(Rh1)通过G蛋白偶联激活磷脂酶C (PLC)将光子吸收转化为电信号。质膜中的Rh1水平对正常的光敏感性至关重要。在这项研究中,我们报道了蛋白激酶D (dPKD)调节成人光感受器中Rh1的稳态。虽然在dPKDH低变形(dPKDH)中眼睛发育和视网膜结构不受影响,但它表现出Rh1水平升高。令人惊讶的是,尽管Rh1水平升高,但在这些果蝇对光的电反应中没有观察到缺陷。相比之下,另一种光感受器质膜跨膜蛋白的水平,瞬时受体电位(TRP)在dPKDH中没有改变。我们的研究结果表明,dPKD对于眼睛发育是必不可少的,但对于维持成人光感受器中的Rh1水平是必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maintenance of Rhodopsin levels in Drosophila photoreceptor and phototransduction requires Protein Kinase D.

Maintenance of Rhodopsin levels in Drosophila photoreceptor and phototransduction requires Protein Kinase D.

Maintenance of Rhodopsin levels in Drosophila photoreceptor and phototransduction requires Protein Kinase D.

Maintenance of Rhodopsin levels in Drosophila photoreceptor and phototransduction requires Protein Kinase D.

During Drosophila phototransduction, the G protein coupled receptor (GPCR) Rhodopsin (Rh1) transduces photon absorption into electrical signal via G-protein coupled activation of phospholipase C (PLC). Rh1 levels in the plasma membrane are critical for normal sensitivity to light. In this study, we report that Protein Kinase D (dPKD) regulates Rh1 homeostasis in adult photoreceptors. Although eye development and retinal structure are unaffected in the dPKD hypomorph (dPKDH), it exhibited elevated levels of Rh1. Surprisingly, despite having elevated levels of Rh1, no defect was observed in the electrical response to light in these flies. By contrast the levels of another transmembrane protein of the photoreceptor plasma membrane, Transient receptor potential (TRP) was not altered in dPKDH. Our results indicate that dPKD is dispensable for eye development but is required for maintaining Rh1 levels in adult photoreceptors.

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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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