Program in Epithelial Biology, Stanford University School of Medicine Stanford, CA, 94305, USA.
Program in Epithelial Biology, Stanford University School of Medicine Stanford, CA, 94305, USA.
Curr Opin Cell Biol. 2021 Feb;68:173-180. doi: 10.1016/j.ceb.2020.10.006. Epub 2020 Nov 20.
The nucleoskeleton has been associated with partitioning the genome into active and inactive compartments that dictate local transcription factor (TF) activity. However, recent data indicate that the nucleoskeleton and TFs reciprocally influence each other in dynamic TF trafficking pathways through the functions of LEM proteins. While the conserved peripheral recruitment of TFs by LEM proteins has been viewed as a mechanism of repressing transcription, a diversity of release mechanisms from the lamina suggest this compartment serves as a refuge for nuclear TF accumulation for rapid mobilization and signal stability. Detailed mechanisms suggest that TFs toggle between nuclear lamina refuge and nuclear matrix lamin-LEM protein complexes at sites of active transcription. In this review we will highlight emerging LEM functions acting at the interface of chromatin and nucleoskeleton to create TF trafficking networks.
核骨架与将基因组分隔成有活性和无活性区室相关,这些区室决定局部转录因子 (TF) 的活性。然而,最近的数据表明,核骨架和 TF 通过 LEM 蛋白的功能在动态 TF 运输途径中相互影响。虽然 LEM 蛋白对 TF 的保守外周募集被视为抑制转录的一种机制,但从核纤层释放的多种机制表明,该隔室充当核 TF 积累的避难所,以实现快速动员和信号稳定性。详细的机制表明,TF 在活性转录位点在核纤层避难所和核基质 lamin-LEM 蛋白复合物之间切换。在这篇综述中,我们将重点介绍在染色质和核骨架界面起作用的新兴 LEM 功能,以创建 TF 运输网络。