Research Group Anatomy, Division of Human Medicine, School of Medicine and Health Sciences, Carl von Ossietzky University Oldenburg, 26129 Oldenburg, Germany.
Institute of Anatomy, Rostock University Medical Center, 18057 Rostock, Germany.
Int J Mol Sci. 2022 Oct 27;23(21):13007. doi: 10.3390/ijms232113007.
The functional importance of neuronal differentiation of the transmembrane proteins' plasticity-related genes 3 (PRG3) and 5 (PRG5) has been shown. Although their sequence is closely related, they promote different morphological changes in neurons. PRG3 was shown to promote neuritogenesis in primary neurons; PRG5 contributes to spine induction in immature neurons and the regulation of spine density and morphology in mature neurons. Both exhibit intracellularly located C-termini of less than 50 amino acids. Varying C-termini suggested that these domains shape neuronal morphology differently. We generated mutant EGFP-fusion proteins in which the C-termini were either swapped between PRG3 and PRG5, deleted, or fused to another family member, plasticity-related gene 4 (PRG4), that was recently shown to be expressed in different brain regions. We subsequently analyzed the influence of overexpression in immature neurons. Our results point to a critical role of the PRG3 and PRG5 C-termini in shaping early neuronal morphology. However, the results suggest that the C-terminus alone might not be sufficient for promoting the morphological effects induced by PRG3 and PRG5.
已经证明了跨膜蛋白可塑性相关基因 3(PRG3)和 5(PRG5)的神经元分化的功能重要性。尽管它们的序列密切相关,但它们促进神经元的不同形态变化。PRG3 被证明能促进原代神经元的神经突生成;PRG5 有助于未成熟神经元的棘突诱导以及成熟神经元的棘突密度和形态的调节。两者都表现出细胞内的 C 端小于 50 个氨基酸。不同的 C 端表明这些结构域以不同的方式塑造神经元形态。我们生成了突变的 EGFP 融合蛋白,其中 C 端在 PRG3 和 PRG5 之间交换、缺失或融合到另一个最近在不同脑区表达的家族成员可塑性相关基因 4(PRG4)上。随后,我们分析了在未成熟神经元中过表达的影响。我们的结果表明 PRG3 和 PRG5 C 端在塑造早期神经元形态中起着关键作用。然而,结果表明 C 端本身可能不足以促进 PRG3 和 PRG5 诱导的形态效应。