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比较在不间断或间断培养箱中培养的人类胚胎的 DNA 甲基化图谱。

Comparison of DNA methylation profiles of human embryos cultured in either uninterrupted or interrupted incubators.

机构信息

Chongqing Key Laboratory of Human Embryo Engineering, Center for Reproductive Medicine, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.

Chongqing Clinical Research Center for Reproductive Medicine, Chongqing Health Center for Women and Children, Chongqing, China.

出版信息

J Assist Reprod Genet. 2023 Jan;40(1):113-123. doi: 10.1007/s10815-022-02669-9. Epub 2022 Dec 2.

Abstract

PURPOSE

We aimed to compare the DNA methylation profiles of human embryos cultured in uninterrupted or interrupted incubators.

METHODS

This study included 9 women, ≤ 30 years old (range: 20-30 years), without a history of genetic diseases or smoking, undergoing ICSI treatment, and each woman donated one oocyte. Embryos were randomly assigned to culture in either time-lapse imaging or standard incubators after ICSI. We compared the DNA methylation profiles of human eight-cell embryos cultured in uninterrupted condition using time-lapse imaging (TLI) incubator (EmbryoScope) to those cultured in interrupted culture model using standard incubators (SI, G185 K-System). Nine single-cell whole-genome bisulfite sequencing (WGBS) datasets were analyzed, including four SI-cultured embryos and five TLI-cultured embryos at the eight-cell stage.

RESULTS

A total of 581,140,020 and 732,348,182 clean reads were generated from the TLI and SI groups, respectively. TLI-cultured embryos had similar genome-wide methylation patterns to SI-cultured embryos. There were no significant differences in the methylation and transcription levels of transposable elements and imprinted control regions. Although a total of 198 differentially methylated genes (DMGs) were identified, only five DMGs had significantly different transcription levels between the two groups.

CONCLUSIONS

This is the first study to compare the DNA methylation profiles of embryos cultured in TLI and SI and will provide a foundation for evaluating the safety of TLI application in assisted reproductive technologies. However, further study with a larger cohort of samples was needed for the data validation.

摘要

目的

比较在不间断或间断培养箱中培养的人类胚胎的 DNA 甲基化谱。

方法

本研究纳入 9 名年龄≤30 岁(年龄 20-30 岁)、无遗传疾病或吸烟史、接受 ICSI 治疗的女性,每位女性捐献一枚卵子。胚胎在 ICSI 后随机分配在延时成像或标准培养箱中培养。我们比较了在不间断培养条件下使用延时成像(TLI)培养箱(EmbryoScope)培养的人 8 细胞胚胎与在标准培养箱(SI,G185 K-系统)中培养的中断培养模型的 DNA 甲基化谱。分析了 9 个单细胞全基因组亚硫酸氢盐测序(WGBS)数据集,包括 4 个 SI 培养胚胎和 5 个 TLI 培养胚胎的 8 细胞期。

结果

TLI 和 SI 组分别产生了 581140020 和 732348182 条清洁读取序列。TLI 培养的胚胎与 SI 培养的胚胎具有相似的全基因组甲基化模式。转座元件和印迹控制区的甲基化和转录水平没有显著差异。虽然总共鉴定出 198 个差异甲基化基因(DMGs),但只有 5 个 DMGs 在两组之间的转录水平有显著差异。

结论

这是第一项比较 TLI 和 SI 培养胚胎 DNA 甲基化谱的研究,为评估 TLI 在辅助生殖技术中的应用安全性提供了基础。然而,需要进一步的研究,使用更大的样本队列来验证数据。

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Single-cell DNA methylome sequencing of human preimplantation embryos.人类胚胎植入前单细胞 DNA 甲基组测序。
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