Coordinated Dynamics of RNA Splicing Speckles in the Nucleus

被引:19
|
作者
Zhang, Qiao [1 ]
Kota, Krishna P. [2 ]
Alam, Samer G. [1 ]
Nickerson, Jeffrey A. [3 ]
Dickinson, Richard B. [1 ]
Lele, Tanmay P. [1 ]
机构
[1] Univ Florida, Dept Chem Engn, Bldg 723, Gainesville, FL 32611 USA
[2] Perkin Elmer Inc, Dept Cellular & Tissue Imaging, Waltham, MA USA
[3] Univ Massachusetts, Sch Med, Dept Cell & Dev Biol, Worcester, MA 01605 USA
关键词
INTERCHROMATIN GRANULE CLUSTERS; SC-35; DOMAINS; LIVING CELLS; CHROMATIN; MATRIX; COMPLEX; PROTEIN; TRANSCRIPTION; ORGANIZATION; ASSOCIATION;
D O I
10.1002/jcp.25224
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite being densely packed with chromatin, nuclear bodies and a nucleoskeletal network, the nucleus is a remarkably dynamic organelle. Chromatin loops form and relax, RNA transcripts and transcription factors move diffusively, and nuclear bodies move. We show here that RNA splicing speckled domains (splicing speckles) fluctuate in constrained nuclear volumes and remodel their shapes. Small speckles move in a directed way toward larger speckles with which they fuse. This directed movement is reduced upon decreasing cellular ATP levels or inhibiting RNA polymerase II activity. The random movement of speckles is reduced upon decreasing cellular ATP levels, moderately reduced after inhibition of SWI/SNF chromatin remodeling and modestly increased upon inhibiting RNA polymerase II activity. To define the paths through which speckles can translocate in the nucleus, we generated a pressure gradient to create flows in the nucleus. In response to the pressure gradient, speckles moved along curvilinear paths in the nucleus. Collectively, our results demonstrate a new type of ATP-dependent motion in the nucleus. We present a model where recycling splicing factors return as part of small sub-speckles from distal sites of RNA processing to larger splicing speckles by a directed ATP-driven mechanism through interchromatin spaces. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1269 / 1275
页数:7
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