Troponin T3 regulates nuclear localization of the calcium channel Cavβ1a subunit in skeletal muscle

被引:9
|
作者
Zhang, Tan [1 ]
Taylor, Jackson [1 ]
Jiang, Yang [1 ,4 ]
Pereyra, Andrea S. [3 ]
Messi, Maria Laura [1 ]
Wang, Zhong-Min [1 ]
Herenu, Claudia [3 ]
Delbono, Osvaldo [1 ,2 ]
机构
[1] Wake Forest Sch Med, Dept Internal Med Gerontol, Winston Salem, NC 27157 USA
[2] Wake Forest Sch Med, Neurosci Program, Winston Salem, NC 27157 USA
[3] Natl Univ La Plata, Dept Histol, RA-1900 La Plata, Argentina
[4] Peking Univ, Sch & Hosp Stomatol, Dept Oral & Maxillofacial Surg, Beijing 100081, Peoples R China
基金
美国国家卫生研究院;
关键词
Troponin T3; Ca-v beta(1a); Nuclear localization; Skeletal muscle; CARDIAC TROPONIN; CA2+ TRANSIENTS; BETA-SUBUNIT; EXPRESSION; RECEPTOR; TROPOMYOSIN; ISOFORMS; PROTEIN; SINGLE; DIFFERENTIATION;
D O I
10.1016/j.yexcr.2015.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The voltage-gated calcium channel (Ca-v) beta(1a) subunit (Ca-v beta(1a)) plays an important role in excitation-contraction coupling (ECC), a process in the myoplasm that leads to muscle-force generation. Recently, we discovered that the Ca-v beta(1a) subunit travels to the nucleus of skeletal muscle cells where it helps to regulate gene transcription. To determine how it travels to the nucleus, we performed a yeast two-hybrid screening of the mouse fast skeletal muscle cDNA library and identified an interaction with troponin T3 (TnT3), which we subsequently confirmed by co-immunoprecipitation and co-localization assays in mouse skeletal muscle in vivo and in cultured C2C12 muscle cells. Interacting domains were mapped to the leucine zipper domain in TnT3 COOH-terminus (160-244 aa) and Ca-v beta(1a) NH2-terminus (1-99 aa), respectively. The double fluorescence assay in C2C12 cells co-expressing TnT3/DsRed and Ca-v beta(1a)/YFP shows that TnT3 facilitates Ca-v beta(1a) a nuclear recruitment, suggesting that the two proteins play a heretofore unknown role during early muscle differentiation in addition to their classical role in FCC regulation. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:276 / 286
页数:11
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