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人类胚胎植入前发育中小非编码 RNA 图谱。

An atlas of small non-coding RNAs in human preimplantation development.

机构信息

CReATe Fertility Centre, Toronto, ON, Canada.

Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Nat Commun. 2024 Oct 5;15(1):8634. doi: 10.1038/s41467-024-52943-w.

Abstract

Understanding the molecular circuitries that govern early embryogenesis is important, yet our knowledge of these in human preimplantation development remains limited. Small non-coding RNAs (sncRNAs) can regulate gene expression and thus impact blastocyst formation, however, the expression of specific biotypes and their dynamics during preimplantation development remains unknown. Here we identify the abundance of and kinetics of piRNA, rRNA, snoRNA, tRNA, and miRNA from embryonic day (E)3-7 and isolate specific miRNAs and snoRNAs of particular importance in blastocyst formation and pluripotency. These sncRNAs correspond to specific genomic hotspots: an enrichment of the chromosome 19 miRNA cluster (C19MC) in the trophectoderm (TE), and the chromosome 14 miRNA cluster (C14MC) and MEG8-related snoRNAs in the inner cell mass (ICM), which may serve as 'master regulators' of potency and lineage. Additionally, we observe a developmental transition with 21 isomiRs and in tRNA fragment (tRF) codon usage and identify two novel miRNAs. Our analysis provides a comprehensive measure of sncRNA biotypes and their corresponding dynamics throughout human preimplantation development, providing an extensive resource. Better understanding the sncRNA regulatory programmes in human embryogenesis will inform strategies to improve embryo development and outcomes of assisted reproductive technologies. We anticipate broad usage of our data as a resource for studies aimed at understanding embryogenesis, optimising stem cell-based models, assisted reproductive technology, and stem cell biology.

摘要

理解调控早期胚胎发生的分子电路是很重要的,但我们对人类着床前发育中这些电路的了解仍然有限。小非编码 RNA(sncRNA)可以调控基因表达,从而影响囊胚形成,然而,特定生物型的表达及其在着床前发育过程中的动态变化仍不清楚。在这里,我们确定了 piRNA、rRNA、snoRNA、tRNA 和 miRNA 从胚胎日(E)3-7 的丰度和动力学,并分离了在囊胚形成和多能性中特别重要的特定 miRNA 和 snoRNA。这些 sncRNA 对应于特定的基因组热点:滋养外胚层(TE)中第 19 号染色体 miRNA 簇(C19MC)的富集,以及内细胞团(ICM)中第 14 号染色体 miRNA 簇(C14MC)和 MEG8 相关 snoRNA,它们可能作为潜能和谱系的“主调控因子”。此外,我们观察到 21 个同工型和 tRNA 片段(tRF)密码子使用的发育性转变,并鉴定了两个新的 miRNA。我们的分析提供了 sncRNA 生物型及其在人类着床前发育过程中相应动态的全面衡量标准,提供了广泛的资源。更好地了解人类胚胎发生中的 sncRNA 调控程序将为改善胚胎发育和辅助生殖技术的结果提供信息。我们预计我们的数据将被广泛用作旨在理解胚胎发生、优化基于干细胞的模型、辅助生殖技术和干细胞生物学的研究的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218d/11452719/b2f452b58e35/41467_2024_52943_Fig1_HTML.jpg

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