Center for Cell Signaling, University of Virginia, Charlottesville, VA, USA,
Adv Exp Med Biol. 2014;773:309-22. doi: 10.1007/978-1-4899-8032-8_14.
Tpr is a prominent architectural component of the nuclear pore complex that forms the basket-like structure on the nucleoplasmic side of the pore. Tpr, which stands for translocated promoter region, was originally described in the context of oncogenic fusions with the receptor tyrosine kinases Met, TRK, and Raf. Tpr has been since implicated in a variety of nuclear functions, including nuclear transport, chromatin organization, regulation of transcription, and mitosis. More recently, Tpr function has been linked to events including p53 signaling and premature aging in Hutchinson-Gilford Progeria Syndrome (HGPS). Here we provide an overview of the various processes that involve Tpr, and discuss how the levels and localization of a single protein can affect diverse pathways in the cell.
Tpr 是核孔复合体的一个重要结构成分,形成核孔细胞质一侧的篮状结构。Tpr 代表易位启动子区域,最初在与受体酪氨酸激酶 Met、TRK 和 Raf 的致癌融合的背景下被描述。此后,Tpr 被牵连到多种核功能中,包括核运输、染色质组织、转录调控和有丝分裂。最近,Tpr 的功能与包括 p53 信号和 Hutchinson-Gilford 早老综合征(HGPS)中的过早衰老在内的事件相关联。在这里,我们提供了涉及 Tpr 的各种过程的概述,并讨论了单个蛋白质的水平和定位如何影响细胞中的不同途径。