A systematic study of nuclear interactome of C-terminal domain small phosphatase-like 2 using inducible expression system and shotgun proteomics

被引:6
作者
Kang, Nana [1 ]
Koo, JaeHyung [1 ]
Wang, Sen [2 ]
Hur, Sun Jin [3 ]
Bahk, Young Yil [4 ]
机构
[1] DGIST, Dept Brain & Cognit Sci, Daegu 42988, South Korea
[2] Qiqihar Med Univ, Qiqihar City 161006, Heilongjiang, Peoples R China
[3] Chung Ang Univ, Dept Anim Sci & Technol, Anseong 17546, South Korea
[4] Konkuk Univ, Dept Biotechnol, Chungju 27478, South Korea
基金
新加坡国家研究基金会;
关键词
CTD phosphatase; CTDSPL2 inducible HEK293T cell line; CTDSPL2; Immunoprecipitation; Nuclear interactome; RNA-POLYMERASE-II; MOUSE EMBRYONIC FIBROBLASTS; ONCOGENIC RAS; IDENTIFICATION; SCP1; CELL;
D O I
10.5483/BMBRep.2016.49.6.240
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
RNA polymerase II C-terminal domain phosphatases are newly emerging family of phosphatases that contain FCPH domain with Mg+2-binding DXDX(T/V) signature motif. Its subfamily includes small CTD phosphatases (SCPs). Recently, we identified several interacting partners of human SCP1 with appearance of dephosphorylation and O-GlcNAcylation. In this study, using an established cell line with inducible CTDSPL2 protein (a member of the new phosphatase family), proteomic screening was conducted to identify binding partners of CTDSPL2 in nuclear extract through immunoprecipitation of CTDSPL2 with its associated. This approach led to the identification of several interacting partners of CTDSPL2. This will provide a better understanding on CTDSPL2.
引用
收藏
页码:319 / 324
页数:6
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