IGF2BP3 May Contributes to Lung Tumorigenesis by Regulating the Alternative Splicing of PKM

被引:41
作者
Huang Xueqing [1 ]
Zhang Jun [1 ]
Jiang Yueqiang [1 ]
Liao Xin [1 ]
Hu Liya [1 ]
Fang Yuanyuan [1 ]
Zhang Yuting [1 ]
Zeng Hao [1 ]
Wu Hua [1 ]
Liu Jian [1 ]
Yin Tiejun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Geriatr, Tongji Med Coll, Wuhan, Peoples R China
关键词
lung tumorigenesis; IGF2BP3; iRIP-seq; alternative splicing; cancer therapy 3; IMP3; RNA-BINDING PROTEINS; PYRUVATE-KINASE M2; CANCER; IMP3; EXPRESSION; BIOMARKER; IDENTIFICATION; MARKER; ROLES;
D O I
10.3389/fbioe.2020.00679
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA binding proteins (RBPs) play a key role in genome regulation. Here we report the post-transcript regulation of IGF2BP3, which belongs to the insulin-like growth factor 2 mRNA binding protein family. We used iRIP-seq and RNA-seq to analyze the transcript regulation and alternative splicing on IGF2BP3 treated with overexpression cells and control. Overexpressed IGF2BP3 has broadly increased genes expression which involved in G-protein coupled receptor signaling pathway, positive regulation of cell proliferation, and signal transduction. IGF2BP3 regulated alternative splicing of multiple genes mainly clustered at response to hypoxia, negative regulation of transcription, and embryonic development. This study first provides alternative splicing analysis on transcription level of IGF2BP3 regulation, which laid the foundation for later research on IGF2BP3 critical functions.
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页数:12
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