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低等脊椎动物松果体中双稳态色素副视蛋白对转导蛋白的激活作用。

Activation of Transducin by Bistable Pigment Parapinopsin in the Pineal Organ of Lower Vertebrates.

作者信息

Kawano-Yamashita Emi, Koyanagi Mitsumasa, Wada Seiji, Tsukamoto Hisao, Nagata Takashi, Terakita Akihisa

机构信息

Department of Biology and Geosciences, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka, 558-8585, Japan.

Department of Biology and Geosciences, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka, 558-8585, Japan; The OCU Advanced Research Institute for Natural Science and Technology (OCARINA), Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka, 558-8585, Japan; Japan Science and Technology Agency (JST), Precursory Research for Embryonic Science and Technology (PRESTO), Tokyo, Japan.

出版信息

PLoS One. 2015 Oct 22;10(10):e0141280. doi: 10.1371/journal.pone.0141280. eCollection 2015.

Abstract

Pineal organs of lower vertebrates contain several kinds of photosensitive molecules, opsins that are suggested to be involved in different light-regulated physiological functions. We previously reported that parapinopsin is an ultraviolet (UV)-sensitive opsin that underlies hyperpolarization of the pineal photoreceptor cells of lower vertebrates to achieve pineal wavelength discrimination. Although, parapinopsin is phylogenetically close to vertebrate visual opsins, it exhibits a property similar to invertebrate visual opsins and melanopsin: the photoproduct of parapinopsin is stable and reverts to the original dark states, demonstrating the nature of bistable pigments. Therefore, it is of evolutionary interest to identify a phototransduction cascade driven by parapinopsin and to compare it with that in vertebrate visual cells. Here, we showed that parapinopsin is coupled to vertebrate visual G protein transducin in the pufferfish, zebrafish, and lamprey pineal organs. Biochemical analyses demonstrated that parapinopsins activated transducin in vitro in a light-dependent manner, similar to vertebrate visual opsins. Interestingly, transducin activation by parapinopsin was provoked and terminated by UV- and subsequent orange-lights irradiations, respectively, due to the bistable nature of parapinopsin, which could contribute to a wavelength-dependent control of a second messenger level in the cell as a unique optogenetic tool. Immunohistochemical examination revealed that parapinopsin was colocalized with Gt2 in the teleost, which possesses rod and cone types of transducin, Gt1, and Gt2. On the other hand, in the lamprey, which does not possess the Gt2 gene, in situ hybridization suggested that parapinopsin-expressing photoreceptor cells contained Gt1 type transducin GtS, indicating that lamprey parapinopsin may use GtS in place of Gt2. Because it is widely accepted that vertebrate visual opsins having a bleaching nature have evolved from non-bleaching opsins similar to parapinopsin, these results implied that ancestral bistable opsins might acquire coupling to the transducin-mediated cascade and achieve light-dependent hyperpolarizing response of the photoreceptor cells.

摘要

低等脊椎动物的松果体器官含有几种光敏分子,即视蛋白,它们被认为参与不同的光调节生理功能。我们之前报道过,副视蛋白是一种对紫外线(UV)敏感的视蛋白,它是低等脊椎动物松果体光感受器细胞超极化的基础,以实现松果体的波长辨别。尽管副视蛋白在系统发育上与脊椎动物视觉视蛋白接近,但它表现出与无脊椎动物视觉视蛋白和黑视蛋白相似的特性:副视蛋白的光产物是稳定的,并恢复到原始暗态,这证明了双稳态色素的性质。因此,确定由副视蛋白驱动的光转导级联并将其与脊椎动物视觉细胞中的光转导级联进行比较具有进化意义。在这里,我们表明在河豚、斑马鱼和七鳃鳗的松果体器官中,副视蛋白与脊椎动物视觉G蛋白转导蛋白偶联。生化分析表明,副视蛋白在体外以光依赖的方式激活转导蛋白,类似于脊椎动物视觉视蛋白。有趣的是,由于副视蛋白的双稳态性质,副视蛋白对转导蛋白的激活分别由紫外线和随后的橙光照射引发和终止,这可能作为一种独特的光遗传学工具,有助于对细胞中第二信使水平进行波长依赖性控制。免疫组织化学检查显示,在拥有视杆和视锥类型转导蛋白Gt1和Gt2的硬骨鱼中,副视蛋白与Gt2共定位。另一方面,在不具有Gt2基因的七鳃鳗中,原位杂交表明表达副视蛋白的光感受器细胞含有Gt1型转导蛋白GtS,这表明七鳃鳗副视蛋白可能使用GtS来替代Gt2。因为人们普遍认为具有漂白性质的脊椎动物视觉视蛋白是从类似于副视蛋白的非漂白视蛋白进化而来的,这些结果意味着祖先的双稳态视蛋白可能获得了与转导蛋白介导的级联的偶联,并实现了光感受器细胞的光依赖性超极化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a2e/4619617/7b8d44a66c6e/pone.0141280.g001.jpg

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