Núcleo de Cognição e Sistemas Complexos, Centro de Matemática, Computação e Cognição, Universidade Federal do ABC, Santo André, SP, Brasil.
PLoS One. 2013 May 20;8(5):e56908. doi: 10.1371/journal.pone.0056908. Print 2013.
In the nervous system, control of gene expression by microRNAs (miRNAs) has been investigated in fundamental processes, such as development and adaptation to ambient demands. The action of these short nucleotide sequences on specific genes depends on intracellular concentration, which in turn reflects the balance of biosynthesis and degradation. Whereas mechanisms underlying miRNA biogenesis has been investigated in recent studies, little is known about miRNA-stability related proteins. We first detected two genes in the retina that have been associated to miRNA stability, XRN2 and PAPD4. These genes are highly expressed during retinal development, however with distinct subcellular localization. We investigated whether these proteins are regulated during specific phases of the cell cycle. Combined analyses of nuclei position in neuroblastic layer and labeling using anti-cyclin D1 revealed that both proteins do not accumulate in S or M phases of the cell cycle, being poorly expressed in progenitor cells. Indeed, XRN2 and PAPD4 were observed mainly after neuronal differentiation, since low expression was also observed in astrocytes, endothelial and microglial cells. XRN2 and PAPD4 are expressed in a wide variety of neurons, including horizontal, amacrine and ganglion cells. To evaluate the functional role of both genes, we carried out experiments addressed to the retinal adaptation in response to different ambient light conditions. PAPD4 is upregulated after 3 and 24 hours of dark- adaptation, revealing that accumulation of this protein is governed by ambient light levels. Indeed, the fast and functional regulation of PAPD4 was not related to changes in gene expression, disclosing that control of protein levels occurs by post-transcriptional mechanisms. Furthermore, we were able to quantify changes in PAPD4 in specific amacrine cells after dark -adaptation, suggesting for circuitry-related roles in visual perception. In summary, in this study we first described the ontogenesis and functional expression of these two miRNA-stability related proteins in the retina.
在神经系统中,微小 RNA(miRNAs)对基因表达的控制已在发育和适应环境需求等基本过程中进行了研究。这些短核苷酸序列对特定基因的作用取决于细胞内浓度,而细胞内浓度又反映了生物合成和降解的平衡。尽管最近的研究已经探讨了 miRNA 生物发生的机制,但关于 miRNA 稳定性相关蛋白知之甚少。我们首先在视网膜中检测到与 miRNA 稳定性相关的两个基因,即 XRN2 和 PAPD4。这些基因在视网膜发育过程中高度表达,但具有不同的亚细胞定位。我们研究了这些蛋白质是否在细胞周期的特定阶段受到调节。通过神经母细胞层中核位置的联合分析和抗细胞周期蛋白 D1 的标记显示,这两种蛋白质都不会在 S 期或 M 期的细胞周期中积累,在祖细胞中表达水平较低。事实上,XRN2 和 PAPD4主要在神经元分化后表达,因为在星形胶质细胞、内皮细胞和小胶质细胞中也观察到低表达。XRN2 和 PAPD4在广泛的神经元中表达,包括水平细胞、无长突细胞和节细胞。为了评估这两个基因的功能作用,我们进行了实验,以研究视网膜对不同环境光照条件的适应。PAPD4 在暗适应 3 小时和 24 小时后上调,表明该蛋白的积累受环境光照水平的调控。事实上,PAPD4 的快速和功能性调节与基因表达的变化无关,揭示了蛋白质水平的控制是通过转录后机制发生的。此外,我们能够在暗适应后定量特定无长突细胞中 PAPD4 的变化,这表明它在视觉感知中具有与电路相关的作用。总之,在这项研究中,我们首次描述了这两种与 miRNA 稳定性相关的蛋白质在视网膜中的发生和功能表达。