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基于转录组学和蛋白质组学综合分析的胎盘植入谱系中枢纽基因的系统鉴定

Systematic Identification of Hub Genes in Placenta Accreta Spectrum Based on Integrated Transcriptomic and Proteomic Analysis.

作者信息

Chen Bingnan, Wang Di, Bian Yue, Li Jiapo, Yang Tian, Li Na, Qiao Chong

机构信息

Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.

Key Laboratory of Maternal-Fetal Medicine of Liaoning Province, China Medical University, Shenyang, China.

出版信息

Front Genet. 2020 Sep 15;11:551495. doi: 10.3389/fgene.2020.551495. eCollection 2020.

Abstract

Placenta accreta spectrum (PAS) is a pathological condition of the placenta with abnormal adhesion or invasion of the placental villi to the uterine wall, which is associated with a variety of adverse maternal and fetal outcomes. Although some PAS-related molecules have been reported, the underlying regulatory mechanism is still unclear. Compared with the study of single gene or pathway, omics study, using advanced sequencing technology and bioinformatics methods, can increase our systematic understanding of diseases. In this study, placenta tissues from 5 patients with PAS and 5 healthy pregnant women were collected for transcriptomic and proteomic sequencing and integrated analysis. A total of 728 messenger RNAs and 439 proteins were found to be significantly different between PAS group and non-PAS group, in which 23 hub genes were differentially expressed in both transcriptome and proteome. Functional enrichment analysis showed that the differentially expressed genes were mainly related to cell proliferation, migration and vascular development. Totally 18 long non-coding RNA were found that might regulate the expression of hub genes. Many kinds of single nucleotide polymorphism, alternative splicing and gene fusion of hub genes were detected. This is the first time to systematically explore the hub genes and gene structure variations of PAS through integrated omics analysis, which provided a genetic basis for further in-depth study on the underlying regulatory mechanism of PAS.

摘要

胎盘植入谱系(PAS)是一种胎盘的病理状态,胎盘绒毛对子宫壁存在异常黏附或侵入,这与多种不良母婴结局相关。尽管已有一些与PAS相关的分子被报道,但其潜在的调控机制仍不清楚。与单基因或单途径研究相比,组学研究利用先进的测序技术和生物信息学方法,能够增强我们对疾病的系统性认识。在本研究中,收集了5例PAS患者和5例健康孕妇的胎盘组织进行转录组和蛋白质组测序及综合分析。结果发现,PAS组和非PAS组之间共有728条信使核糖核酸和439种蛋白质存在显著差异,其中23个枢纽基因在转录组和蛋白质组中均有差异表达。功能富集分析表明,差异表达基因主要与细胞增殖、迁移和血管发育相关。共发现18条长链非编码核糖核酸可能调控枢纽基因的表达。检测到枢纽基因存在多种单核苷酸多态性、可变剪接和基因融合。这是首次通过综合组学分析系统地探索PAS的枢纽基因和基因结构变异,为进一步深入研究PAS的潜在调控机制提供了遗传学基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fb/7522549/25844bc3c4e6/fgene-11-551495-g001.jpg

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