内源性IFITM3敲低靶向的差异表达转录本的鉴定

Identification of differentially expressed transcripts targeted by the knockdown of endogenous IFITM3.

作者信息

Shen Chen, Li Ying-Jia, Yin Qing-Qin, Jiao Wei-Wei, Li Qin-Jing, Xiao Jing, Sun Lin, Xu Fang, Li Jie-Qiong, Qi Hui, Shen A-Dong

机构信息

Key Laboratory of Major Diseases in Children, Ministry of Education, National Key Discipline of Pediatrics, National Clinical Research Center for Respiratory Diseases, Beijing Key Laboratory of Pediatric Respiratory Infection Diseases, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Beijing 100045, P.R. China.

出版信息

Mol Med Rep. 2016 Nov;14(5):4367-4373. doi: 10.3892/mmr.2016.5777. Epub 2016 Sep 26.

Abstract

Interferon inducible transmembrane protein 3 (IFITM3) is a double transmembrane protein. As a member of the IFITM family, IFITM3 can be upregulated by interferon (IFN) to be involved in various biological processes. In order to determine whether gene expression profiles can be altered by a lack of IFITM3, the present study used shRNAs lentivirus for knocking down the endogenous expression of IFITM3 in human HeLa cells and human whole genome microarrays to obtain gene expression profiles. A total of 1,011 downregulated transcripts and 615 upregulated transcripts were identified using the Agilent expression platform. The identified transcripts were involved in multiple pathways, including the complement pathways, and the antigen processing and presentation pathway. The present study identified the transcripts, which were affected by the downregulation of endogenous IFITM3 and the pathways they were involved in. These findings may lead to an improved understanding of the biological functions of IFITM3.

摘要

干扰素诱导跨膜蛋白3(IFITM3)是一种双跨膜蛋白。作为IFITM家族的一员,IFITM3可被干扰素(IFN)上调,从而参与各种生物学过程。为了确定基因表达谱是否会因IFITM3的缺失而改变,本研究使用shRNAs慢病毒敲低人HeLa细胞中IFITM3的内源性表达,并利用人类全基因组微阵列获得基因表达谱。使用安捷伦表达平台共鉴定出1011个下调转录本和615个上调转录本。所鉴定的转录本涉及多种途径,包括补体途径以及抗原加工和呈递途径。本研究鉴定了受内源性IFITM3下调影响的转录本及其所涉及的途径。这些发现可能有助于增进对IFITM3生物学功能的理解。

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