Department of Biochemical Sciences, Sapienza University, 00185 Rome, Italy.
Department of Biology and Biotechnology "Charles Darwin", Sapienza University, 00161 Rome, Italy.
Int J Mol Sci. 2022 May 27;23(11):6058. doi: 10.3390/ijms23116058.
The α-, β- and γ-synucleins are small soluble proteins expressed in the nervous system of mammals and evolutionary conserved in vertebrates. After being discovered in the cartilaginous fish , synucleins have been sequenced in all vertebrates, showing differences in the number of genes and splicing isoforms in different taxa. Although α-, β- and γ-synucleins share high homology in the N-terminal sequence, suggesting their evolution from a common ancestor, the three isoforms also differ in molecular characteristics, expression levels and tissue distribution. Moreover, their functions have yet to be fully understood. Great scientific interest on synucleins mainly derives from the involvement of α-synuclein in human neurodegenerative diseases, collectively named synucleinopathies, which involve the accumulation of amyloidogenic α-synuclein inclusions in neurons and glia cells. Studies on synucleinopathies can take advantage of the development of new vertebrate models other than mammals. Moreover, synuclein expression in non-mammalian vertebrates contribute to clarify the physiological role of these proteins in the evolutionary perspective. In this paper, gene expression levels of α-, β- and γ-synucleins have been analysed in the main organs of adult by qRT-PCR. Moreover, recombinant α-, β- and γ-synucleins were produced to test the specificity of commercial antibodies against α-synuclein used in Western blot and immunohistochemistry. Finally, the secondary structure of synucleins was evaluated by circular dichroism analysis. Results indicate as a good model for studying synucleinopathies, and provide a useful background for future studies on synuclein functions and their evolution in vertebrates.
α-、β-和γ-突触核蛋白是哺乳动物神经系统中表达的小可溶性蛋白,在脊椎动物中进化保守。在软骨鱼类中发现突触核蛋白后,已在所有脊椎动物中对其进行了测序,显示不同分类群中基因和剪接异构体的数量存在差异。尽管α-、β-和γ-突触核蛋白在 N 端序列上具有高度同源性,提示它们来自共同的祖先,但这三种异构体在分子特征、表达水平和组织分布上也存在差异。此外,它们的功能尚未完全了解。人们对突触核蛋白的极大科学兴趣主要源于α-突触核蛋白在人类神经退行性疾病中的参与,统称为突触核蛋白病,其涉及神经元和神经胶质细胞中淀粉样的α-突触核蛋白包涵体的积累。除了哺乳动物之外,研究突触核蛋白病还可以利用新型脊椎动物模型的发展。此外,非哺乳动物脊椎动物中的突触核蛋白表达有助于从进化角度阐明这些蛋白质的生理作用。在本文中,通过 qRT-PCR 分析了成年 主要器官中 α-、β-和γ-突触核蛋白的基因表达水平。此外,还生产了重组的 α-、β-和γ-突触核蛋白,以测试用于 Western blot 和免疫组织化学的针对α-突触核蛋白的商业抗体的特异性。最后,通过圆二色性分析评估了 synuclein 的二级结构。结果表明 是研究突触核蛋白病的良好模型,并为未来研究突触核蛋白在脊椎动物中的功能及其进化提供了有用的背景。