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Differential expression profiles of long non-coding RNAs during the mouse pronuclear stage under normal gravity and simulated microgravity

机译:正常重力和模拟微重力作用下小鼠原核期长非编码RNA的差异表达谱

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摘要

Pronuclear migration, which is the initial stage of embryonic development and the marker of zygote formation, is a crucial process during mammalian preimplantation embryonic development. Recent studies have revealed that long non-coding RNAs (lncRNAs) serve an important role in early embryonic development. However, the functional regulation of lncRNAs in this process has yet to be elucidated, largely due to the difficulty of assessing gene expression alterations during the very short time in which pronuclear migration occurs. It has previously been reported that migration of the pronucleus of a zygote can be obstructed by simulated microgravity. To investigate pronuclear migration in mice, a rotary cell culture system was employed, which generates simulated microgravity, in order to interfere with murine pronuclear migration. Subsequently, lncRNA sequencing was performed to investigate the mechanism underlying this process. In the present study, a comprehensive analysis of lncRNA profile during the mouse pronuclear stage was conducted, in which 3,307 lncRNAs were identified based on single-cell RNA sequencing data. Furthermore, 52 lncRNAs were identified that were significantly differentially expressed. Subsequently, 10 lncRNAs were selected for validation by reverse transcription-quantitative polymerase chain reaction, in which the same relative expression pattern was observed. The results revealed that 12 lncRNAs (lnc006745, lnc007956, lnc013100, lnc013782, lnc017097, lnc019869, lnc025838, lnc027046, lnc005454, lnc007956, lnc019410 and lnc019607), with tubulin β 4B class IVb or actinin α 4 as target genes, may be associated with the expression of microtubule and microfilament proteins. Binding association was confirmed using a dual-luciferase reporter assay. Finally, Gene Ontology analysis revealed that the target genes of the differentially expressed lncRNAs participated in cellular processes associated with protein transport, binding, catalytic activity, membrane-bounded organelle, protein complex and the cortical cytoskeleton. These findings suggested that these lncRNAs may be associated with migration of the mouse pronucleus.
机译:前核迁移是胚胎发育的初始阶段,是合子形成的标志,是哺乳动物植入前胚胎发育的关键过程。最近的研究表明,长的非编码RNA(lncRNA)在早期胚胎发育中起重要作用。然而,lncRNAs在此过程中的功能调节尚待阐明,这主要是由于在发生前核迁移的非常短的时间内很难评估基因表达的变化。以前已经报道过,合子原核的迁移可以通过模拟的微重力来阻止。为了研究小鼠中的原核迁移,采用了旋转细胞培养系统,该系统会产生模拟的微重力,以干扰鼠原核的迁移。随后,进行了lncRNA测序,以研究该过程的潜在机制。在本研究中,对小鼠原核阶段的lncRNA谱进行了全面分析,其中基于单细胞RNA测序数据鉴定出3,307个lncRNA。此外,鉴定出52个显着差异表达的lncRNA。随后,选择10个lncRNA用于通过逆转录-定量聚合酶链反应的验证,其中观察到相同的相对表达模式。结果显示,以微管蛋白β4B类IVb或肌动蛋白α4为靶基因的12种lncRNA(lnc006745,lnc007956,lnc013100,lnc013782,lnc017097,lnc019869,lnc025838,lnc027046,lnc005454,lnc007956,lnc019410和lnc019607)可能与微管蛋白β4B类IVb或肌动蛋白α4相关。微管和微丝蛋白的表达。使用双萤光素酶报告基因测定证实结合缔合。最后,基因本体论分析显示差异表达的lncRNA的靶基因参与了与蛋白质转运,结合,催化活性,膜结合细胞器,蛋白质复合物和皮质细胞骨架相关的细胞过程。这些发现表明这些lncRNA可能与小鼠原核的迁移有关。

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