首页> 外文期刊>International journal of biological sciences >Transmissible Gastroenteritis Virus (TGEV) Infection Alters the Expression of Cellular MicroRNA Species That Affect Transcription of TGEV Gene 7
【24h】

Transmissible Gastroenteritis Virus (TGEV) Infection Alters the Expression of Cellular MicroRNA Species That Affect Transcription of TGEV Gene 7

机译:传染性胃肠炎病毒(TGEV)感染改变了影响TGEV基因7转录的细胞MicroRNA种类的表达。

获取原文
           

摘要

Transmissible gastroenteritis virus (TGEV) is a member of Coronaviridae family. TGEV infection has emerged as a major cause of severe gastroenteritis and leads to alterations of many cellular processes. Meanwhile, the pathogenic mechanism of TGEV is still unclear. microRNAs (miRNAs) are a novel class of small non-coding RNAs which are involved in the regulation of numerous biological processes such as viral infection and cell apoptosis. Accumulating data show that miRNAs are involved in the process of coronavirus infection such as replication of severe acute respiratory syndrome coronavirus (SARS-CoV). However, the link between miRNAs and TGEV infection is unknown. In this study, we performed microRNA microarray assay and predicted targets of altered miRNAs. The results showed TGEV infection caused the change of miRNAs profile. Then we selected miR-4331 for further analysis and subsequently identified cell division cycle-associated protein 7 (CDCA7) as the target of miR-4331. Moreover, miR-4331 showed the ability to inhibit transcription of TGEV gene 7 (a non-structure gene) via directly targeting CDCA7. In conclusion, differentially expressed miR-4331 that is caused by TGEV infection can suppress transcription of TGEV gene 7 via targeting cellular CDCA7. Our key finding is that TGEV selectively manipulates the expression of some cellular miRNAs to regulate its subgenomic transcription.
机译:传播性胃肠炎病毒(TGEV)是冠状病毒科的成员。 TGEV感染已成为严重胃肠炎的主要原因,并导致许多细胞过程的改变。同时,TGEV的致病机制仍不清楚。微小RNA(miRNA)是一类新型的小型非编码RNA,涉及许多生物过程的调控,例如病毒感染和细胞凋亡。越来越多的数据表明,miRNA参与了冠状病毒感染的过程,例如严重急性呼吸系统综合症冠状病毒(SARS-CoV)的复制。但是,miRNA与TGEV感染之间的联系尚不清楚。在这项研究中,我们进行了microRNA微阵列分析,并预测了改变的miRNA的靶标。结果表明TGEV感染引起miRNAs谱的改变。然后,我们选择了miR-4331进行进一步分析,随后确定了与细胞分裂周期相关的蛋白7(CDCA7)作为miR-4331的靶标。而且,miR-4331显示出通过直接靶向CDCA7抑制TGEV基因7(非结构基因)转录的能力。总之,由TGEV感染引起的差异表达的miR-4331可通过靶向细胞CDCA7抑制TGEV基因7的转录。我们的关键发现是TGEV选择性操纵某些细胞miRNA的表达以调节其亚基因组转录。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号