János Szentágothai Research Centre, University of Pécs, Pecs, Hungary.
Department of General and Environmental Microbiology, University of Pécs, Pecs, Hungary.
Cell Mol Neurobiol. 2023 Aug;43(6):2963-2974. doi: 10.1007/s10571-023-01347-3. Epub 2023 Apr 21.
The morphogenesis of the mammalian retina depends on the precise control of gene expression during development. Small non-coding RNAs, including microRNAs play profound roles in various physiological and pathological processes via gene expression regulation. A systematic analysis of the expression profile of small non-coding RNAs in developing Wistar rat retinas (postnatally day 5 (P5), P7, P10, P15 and P21) was executed using IonTorrent PGM next-generation sequencing technique to reveal the crucial players in the early postnatal retinogenesis. Our analysis reveals extensive regulatory potential of microRNAs during retinal development. We found a group of microRNAs that show constant high abundance (miR-19, miR-101; miR-181, miR-183, miR-124 and let-7) during the development process. Others are present only in the early stages (miR-20a, miR-206, miR-133, miR-466, miR-1247, miR-3582), or at later stages (miR-29, miR-96, miR-125, miR-344 or miR-664). Further miRNAs were detected which are differentially expressed in time. Finally, pathway enrichment analysis has revealed 850 predicted target genes that mainly participate in lipid-, amino acid- and glycan metabolisms in the examined time-period (P5-P21). P5-P7 transition revealed the importance of miRNAs in glutamatergic synapse and gap junction pathways. Significantly downregulated miRNAs rno-miR-30c1 and 2, rno-miR-205 and rno-miR-503 were detected to target Prkx (ENSRNOG00000003696), Adcy6 (ENSRNOG00000011587), Gnai3 (ENSRNOG00000019465) and Gja1 (ENSRNOG00000000805) genes. The dataset described here will be a valuable resource for clarifying new regulatory mechanisms for retinal development and will greatly contribute to our understanding of the divergence and function of microRNAs.
哺乳动物视网膜的形态发生依赖于发育过程中基因表达的精确控制。小非编码 RNA,包括 microRNAs,通过基因表达调控在各种生理和病理过程中发挥着深远的作用。本研究采用 IonTorrent PGM 下一代测序技术,对发育中的 Wistar 大鼠视网膜(出生后第 5 天(P5)、P7、P10、P15 和 P21)中小非编码 RNA 的表达谱进行了系统分析,以揭示早期出生后视网膜发生过程中的关键调控因子。我们的分析揭示了 microRNAs 在视网膜发育过程中的广泛调控潜力。我们发现了一组在发育过程中始终高度丰富的 microRNAs(miR-19、miR-101、miR-181、miR-183、miR-124 和 let-7)。其他 microRNAs 仅在早期阶段存在(miR-20a、miR-206、miR-133、miR-466、miR-1247、miR-3582),或在晚期阶段存在(miR-29、miR-96、miR-125、miR-344 或 miR-664)。进一步检测到在时间上差异表达的 microRNAs。最后,通路富集分析揭示了在研究时间段(P5-P21)内主要参与脂质、氨基酸和聚糖代谢的 850 个预测靶基因。P5-P7 过渡揭示了 microRNAs 在谷氨酸能突触和缝隙连接途径中的重要性。显著下调的 microRNAs rno-miR-30c1 和 2、rno-miR-205 和 rno-miR-503 被检测到靶向 Prkx(ENSRNOG00000003696)、Adcy6(ENSRNOG00000011587)、Gnai3(ENSRNOG00000019465)和 Gja1(ENSRNOG00000000805)基因。本研究中描述的数据集将成为阐明视网膜发育新调控机制的宝贵资源,并将极大地促进我们对 microRNAs 分化和功能的理解。