Post-transcriptional regulation in early cell fate commitment of germ layers.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-03-08 DOI:10.1186/s12864-025-11400-8
Rubens Gomes-Júnior, Cintia Delai da Silva Horinouchi, Aruana Fagundes Fiuza Hansel-Fröse, Annanda Lyra Ribeiro, Isabela Tiemy Pereira, Lucia Spangenberg, Bruno Dallagiovanna
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引用次数: 0

Abstract

Background: Cell differentiation during development is orchestrated by precisely coordinated gene expression programs. While some regulatory mechanisms are well understood, there is a significant room to explore unresolved aspects of lineage choice and cell-fate decisions, as many events in these processes are still not fully elucidated. Given that, gene expression is influenced not only by transcriptional control but also by post-transcriptional events. Here, we described the presence of post-transcriptional regulation on gene expression during lineage commitment across all three embryonic germ layers. We employed monolayer differentiation protocols to map early transcriptional and post-transcriptional events in human embryonic stem cell specification. This approach included obtaining representative populations from the three germ layers, followed by sequencing of both polysome-bound and total RNAs.

Results: We characterized our model by its unique expression profile and the presence of specific markers for each differentiation. RNA sequencing revealed a consistent pattern of gene upregulated and downregulated when comparing the transcriptome and translatome during the differentiation of all three germ layers. By comparing these datasets, we identified genes subjected to post-transcriptional regulation in all germ layer differentiations and categorized the nature of this regulation. GO analysis demonstrated that polysome profiling serves as a complementary technique, capturing nuances that may be overlooked when analyzing only the transcriptome. Finally, we directly compared the transcriptome and translatome to identify genes actively recruited to the translation machinery, uncovering unique features specific to each germ layer.

Conclusions: Substantial post-transcriptional modulation was found during germ layer commitment, emphasizing the translatome potency in capturing nuanced gene expression regulation. These findings highlight the post-transcriptional regulation's critical role in early embryonic development, offering new insights into the molecular mechanisms of cell differentiation.

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生殖层早期细胞命运调控的转录后调控。
背景:发育过程中的细胞分化是由精确协调的基因表达程序精心安排的。虽然一些调控机制已被很好地理解,但由于这些过程中的许多事件仍未完全阐明,因此探索谱系选择和细胞命运决定的未解决方面仍有很大的空间。鉴于此,基因表达不仅受到转录控制的影响,还受到转录后事件的影响。在这里,我们描述了在所有三个胚胎胚层谱系承诺过程中基因表达的转录后调控的存在。我们采用单层分化协议来绘制人类胚胎干细胞规范的早期转录和转录后事件。该方法包括从三个胚层获得具有代表性的群体,然后对多体结合rna和总rna进行测序。结果:我们通过其独特的表达谱和每种分化的特定标记物来表征我们的模型。RNA测序结果显示,在三个胚层的分化过程中,转录组和翻译组的基因表达均呈现出一致的上调和下调模式。通过比较这些数据集,我们确定了所有胚层分化中受转录后调控的基因,并对这种调控的性质进行了分类。氧化石墨烯分析表明,多体分析可以作为一种补充技术,捕捉到仅分析转录组时可能被忽视的细微差别。最后,我们直接比较了转录组和翻译组,以识别积极招募到翻译机制中的基因,揭示了每个胚层特有的特征。结论:在胚层承诺过程中发现了大量的转录后调节,强调了翻译组在捕捉细微的基因表达调控方面的效力。这些发现突出了转录后调控在早期胚胎发育中的关键作用,为细胞分化的分子机制提供了新的见解。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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