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Sequence Structure and Expression of Opsins in the Monochromatic Stomatopod Squilla empusa

机译:单色拟足类Smilla empusa中视蛋白的序列结构和表达

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摘要

Most stomatopod crustaceans have complex retinas in their compound eyes, with up to 16 spectral types of photoreceptors, but members of the superfamily Squilloidea have much simpler retinas, thought to contain a single photoreceptor spectral class. In the Atlantic stomatopod Squilla empusa, microspectrophotometry shows that all photoreceptors absorb light maximally at 517 nm, indicating that a single visual pigment is present in all photoreceptors in the retina. However, six distinct, but partial, long wavelength sensitive (LWS) opsin transcripts, which encode the protein component of the visual pigment, have been previously isolated through RT-PCR. In order to investigate the spectral and functional differences among S. empusa’s opsins, we used RT-PCR to complete the 3′ end of sequences for five of the six expressed opsins. The extended sequences spanned from the first transmembrane (TM1) helix to the 3′ end of the coding region. Using homology-based modeling, we predicted the three-dimensional structure of the amino acid translation of the S. empusa opsins. Based on these analyses, S. empusa LWS opsins share a high sequence identity in TM regions and in amino acids within 15 Å of the chromophore-binding lysine on TM helix 7 (TM7), suggesting that these opsins produce spectrally similar visual pigments in agreement with previous results. However, we propose that these spectrally similar opsins differ functionally, as there are non-conservative amino acid substitutions found in intracellular loop 2 (ICL2) and TM5/ICL3, which are critical regions for G-protein binding, and substitutions in extracellular regions suggest different chromophore attachment affinities. In situ hybridization of two of the opsins (Se5 and Se6) revealed strong co-expression in all photoreceptors in both midband and peripheral regions of the retina as well as in selected ocular and cerebral ganglion neuropils. These data suggest the expression of multiple opsins—likely spectrally identical, but functionally different—in multiple types of neuronal cells in S. empusa. This suggests that the multiple opsins characteristic of other stomatopod species may have similar functional specialization.
机译:大多数口足类甲壳类动物的复眼具有复杂的视网膜,具有多达16种光谱类型的感光细胞,但是超家族鳞翅目动物的成员具有更简单的视网膜,认为它们包含单个感光细胞光谱类别。显微光度法显示,在大西洋气孔足类鱿鱼中,所有感光体在517nm处最大吸收光,这表明视网膜中的所有感光体中都存在一种视觉色素。但是,先前已通过RT-PCR分离了六种截然不同但局部的长波长敏感(LWS)视蛋白转录本,它们编码视觉色素的蛋白质成分。为了研究欧洲链霉菌视蛋白之间的光谱和功能差异,我们使用了RT-PCR来完成六个表达视蛋白中的五个的3'末端序列。扩展序列从第一个跨膜(TM1)螺旋延伸到编码区的3'端。使用基于同源性的建模,我们预测了S. empusa opsins氨基酸翻译的三维结构。基于这些分析,天麻链球菌LWS视蛋白在TM区域和TM螺旋7(TM7)上发色团结合赖氨酸的15Å内的氨基酸具有较高的序列同一性,表明这些视蛋白一致产生光谱相似的视觉色素。与以前的结果。但是,我们建议这些光谱相似的视蛋白在功能上有所不同,因为在细胞内环2(ICL2)和TM5 / ICL3中发现了非保守氨基酸取代,这是G蛋白结合的关键区域,而在细胞外区域中的取代表明不同的发色团亲和力。两种视蛋白(Se5和Se6)的原位杂交显示,在视网膜中带和周边区域以及选定的眼和脑神经节神经纤维丛中,所有感光细胞均具有强共表达。这些数据表明,在视神经链球菌的多种类型的神经元细胞中,多种视蛋白的表达可能在光谱上是相同的,但在功能上是不同的。这表明其他气孔足动物的多种视蛋白可能具有相似的功能专长。

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