RBM4 modulates the proliferation and expression of inflammatory factors via the alternative splicing of regulatory factors in HeLa cells

被引:0
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作者
Wei-Yang Wang
Weili Quan
Fan Yang
Ya-Xun Wei
Jia-Jun Chen
Han Yu
Jie Xie
Yi Zhang
Zhan-Fei Li
机构
[1] Huazhong University of Science and Technology,Trama Center/Department of Emergency and Trauma Surgery, Tongji Hospital Tongji Medical College
[2] ABLife Inc.,Center for Genome Analysis
[3] ABLife Inc.,Laboratory for Genome Regulation and Human Health
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关键词
RBM4; Overexpression; Gene expression profile; Differentially expressed genes; Inflammatory response; Alternative splicing;
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摘要
Regulatory factors function by modulating a variety of cascade mechanisms in cells. RBM4 is a multifunctional RNA-binding protein in post-transcriptional gene regulation. Cytoplasmic RBM4 interacts with Ago2 to regulate inflammatory responses by affecting mRNA decay and cap-dependent translation. However, it is unclear whether RBM4 functions in inflammation regulation by its splicing factor role. Here, the cell biology, gene expression profile and alternative splicing pattern of HeLa cells with RBM4 overexpression (RBM-OE) were compared with the control. The results showed that RBM4-OE inhibited proliferation. RBM4-OE extensively affects the transcriptional level of genes involved in cell surface receptor signalling pathway, inflammatory responses and the response to lipopolysaccharide. RBM4 broadly regulated the alternative splicing of hundreds of genes with functions of protein binding, helicase activity, DNA binding and transcription co-activator. RBM4-regulated splicing of these genes plays an important role in apoptotic process and gene transcription regulation. As an example, exon inclusion of TNIP1 mediated by RBM4 affects the expression of its targets in inflammatory pathways. These results indicated that RBM4 can mediate the inflammatory response via splicing regulation, which adds to the understanding of the critical role of RBM4 in cancer complicated by inflammation. In conclusion, this study indicated a mechanism in which the dysregulation of alternative splicing can influence cellular biology and lead to various immune-related diseases.
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页码:95 / 106
页数:11
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