Human oncoprotein Musashi-2 N-terminal RNA recognition motif backbone assignment and identification of RNA-binding pocket

被引:10
|
作者
Lan, Lan [1 ]
Xing, Minli [2 ]
Douglas, Justin T. [2 ]
Gao, Philip [3 ]
Hanzlik, Robert P. [4 ]
Xu, Liang [1 ,5 ]
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
[2] Univ Kansas, BioNMR Core Facil, Lawrence, KS 66045 USA
[3] Univ Kansas, Prot Prod Grp, NIH COBRE Prot Struct & Funct, Lawrence, KS 66045 USA
[4] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
[5] Univ Kansas, Med Ctr, Dept Radiat Oncol, Kansas City, KS 66103 USA
基金
美国国家卫生研究院;
关键词
RNA-binding protein; RNA-binding pocket; nuclear magnetic resonance; backbone assignment; Musashi; AGGRESSIVE MYELOID-LEUKEMIA; MESSENGER-RNA; STEM-CELLS; PROTEIN; CANCER; FAMILY; MSI2; SENSITIVITY; METASTASIS; EXPRESSION;
D O I
10.18632/oncotarget.22540
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RNA-binding protein Musashi-2 (MSI2) is a key regulator in stem cells, it is over-expressed in a variety of cancers and its higher expression is associated with poor prognosis. Like Musashi-1, it contains two N-terminal RRMs (RNA-recognition Motifs, also called RBDs (RNA-binding Domains)), RRM1 and RRM2, which mediate the binding to their target mRNAs. Previous studies have obtained the three-dimensional structures of the RBDs of Musashi-1 and the RBD1: RNA complex. Here we show the binding of MSI2-RRM1 to a 15nt Numb RNA in Fluorescence Polarization assay and time resolved Fluorescence Resonance Energy Transfer assay. Using nuclear magnetic resonance (NMR) spectroscopy we assigned the backbone resonances of MSI2-RRM1, and characterized the direct interaction of RRM1 to Numb RNA r(GUAGU). Our NMR titration and structure modeling studies showed that MSI2-RRM1 and MSI1-RBD1 have similar RNA binding events and binding pockets. This work adds significant information to MSI2-RRM1 structure and RNA binding pocket, and contributes to the development of MSI2 specific and MSI1/MSI2 dual inhibitors.
引用
收藏
页码:106587 / 106597
页数:11
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