TRIM5α cytoplasmic bodies are highly dynamic structures

被引:58
作者
Campbell, Edward M.
Dodding, Mark P.
Yap, Melvyn W.
Wu, Xiaolu
Gallois-Montbrun, Sarah
Malim, Michael H.
Stoye, Jonathan P.
Hope, Thomas J. [1 ]
机构
[1] Northwestern Univ, Dept Cell & Mol Biol, Chicago, IL 60611 USA
[2] Univ Illinois, Dept Microbiol & Immunol, Chicago, IL 60612 USA
[3] Natl Inst Med Res, Med Res Council, Div Virol, London NW7 1AA, England
[4] Kings Coll London Sch Med, Guys Hosp, Dept Infect Dis, London SE1 9RT, England
基金
英国医学研究理事会;
关键词
D O I
10.1091/mbc.E06-12-1075
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tripartite motif (TRIM)5 alpha has recently been identified as a host restriction factor that has the ability to block infection by certain retroviruses in a species-dependent manner. One interesting feature of this protein is that it is localized in distinct cytoplasmic clusters designated as cytoplasmic bodies. The potential role of these cytoplasmic bodies in TRIM5 alpha function remains to be defined. By using fluorescent fusion proteins and live cell microscopy, we studied the localization and dynamics of TRIM5 alpha cytoplasmic bodies. This analysis reveals that cytoplasmic bodies are highly mobile, exhibiting both short saltatory movements and unidirectional long-distance movements along the microtubule network. The morphology of the cytoplasmic bodies is also dynamic. Finally, photobleaching and photoactivation analysis reveals that the TRIM5 alpha protein present in the cytoplasmic bodies is very dynamic, rapidly exchanging between cytoplasmic bodies and a more diffuse cytoplasmic population. Therefore, TRIM5 alpha cytoplasmic bodies are dynamic structures more consistent with a role in function or regulation rather than protein aggregates or inclusion bodies that represent dead-end static structures.
引用
收藏
页码:2102 / 2111
页数:10
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