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人类反复受精失败卵母细胞的转录组谱分析。

Transcriptome profiling of human oocytes experiencing recurrent total fertilization failure.

机构信息

Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Center for Comparative Biomedicine, MOE Key Laboratory of Systems Biomedicine, Institute of Systems Biomedicine, SCSB, Shanghai Jiao Tong University (SJTU), Shanghai, 200240, China.

出版信息

Sci Rep. 2018 Dec 17;8(1):17890. doi: 10.1038/s41598-018-36275-6.

Abstract

There exist some patients who face recurrent total fertilization failure during assisted reproduction treatment, but the pathological mechanism underlying is elusive. Here, by using sc-RNA-seq method, the transcriptome profiles of ten abnormally fertilized zygotes were assessed, including five zygotes from one patient with recurrent Poly-PN zygotes, and five zygotes from a patient with pronuclear fusion failure. Four zygotes with three pronuclear (Tri-PN) were collected from four different patients as controls. After that, we identified 951 and 1697 significantly differentially expressed genes (SDEGs) in Poly-PN and PN arrest zygotes, respectively as compared with the control group. KEGG analyses indicated down regulated genes in the Poly-PN group included oocyte meiosis related genes, such as PPP2R1B, YWHAZ, MAD2L1, SPDYC, SKP1 and CDC27, together with genes associated with RNA processing, such as SF3B1, LOC645691, MAGOHB, PHF5A, PRPF18, DDX5, THOC1 and BAT1. In contrast, down regulated genes in the PN arrest group, included cell cycle genes, such as E2F4, DBF4, YWHAB, SKP2, CDC23, SMC3, CDC25A, CCND3, BUB1B, MDM2, CCNA2 and CDC7, together with homologous recombination related genes, such as NBN, XRCC3, SHFM1, RAD54B and RAD51. Thus, our work provides a better understanding of transcriptome profiles underlying RTFF, although it based on a limited number of patients.

摘要

有些患者在辅助生殖治疗中面临反复的完全受精失败,但潜在的病理机制尚不清楚。在这里,我们通过使用 sc-RNA-seq 方法,评估了十个异常受精胚胎的转录组图谱,包括五个来自一个反复出现多原核(Poly-PN)胚胎患者的胚胎,和五个来自核融合失败患者的胚胎。另外还收集了四个不同患者的四枚具有三个原核(Tri-PN)的胚胎作为对照。然后,我们发现 Poly-PN 和 PN 阻滞胚胎与对照组相比,分别有 951 个和 1697 个显著差异表达基因(SDEGs)。KEGG 分析表明,Poly-PN 组下调的基因包括卵母细胞减数分裂相关基因,如 PPP2R1B、YWHAZ、MAD2L1、SPDYC、SKP1 和 CDC27,以及与 RNA 加工相关的基因,如 SF3B1、LOC645691、MAGOHB、PHF5A、PRPF18、DDX5、THOC1 和 BAT1。相比之下,PN 阻滞组下调的基因包括细胞周期基因,如 E2F4、DBF4、YWHAB、SKP2、CDC23、SMC3、CDC25A、CCND3、BUB1B、MDM2、CCNA2 和 CDC7,以及同源重组相关基因,如 NBN、XRCC3、SHFM1、RAD54B 和 RAD51。因此,尽管我们的工作基于有限的患者数量,但它为理解 RTFF 的转录组图谱提供了更好的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4fd/6297154/d705b95220fd/41598_2018_36275_Fig1_HTML.jpg

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