Institut fuer Biochemie, OE4310, Medizinische Hochschule Hannover, Carl-Neuberg-Str, 1, D-30623, Hannover, Germany.
Cell Commun Signal. 2014 Jan 10;12:3. doi: 10.1186/1478-811X-12-3.
Cell growth, differentiation, and commitment to a restricted lineage are guided by a timely expressed set of growth factor/cytokine receptors and their down-stream transcription factor genes. Transcriptional control mechanisms of gene expression during differentiation have been mainly studied by focusing on the cis- and trans-elements in promoters however, the role of mRNA export machinery during differentiation has not been adequately examined. THO (Suppressors of the transcriptional defects of hpr1 delta by overexpression) complex 5 (THOC5) is a member of THO complex which is a subcomplex of the transcription/export complex (TREX). THOC5 is evolutionarily conserved in higher eukaryotes, however the exact roles of THOC5 in transcription and mRNA export are still unclear. In this review, we focus on recently uncovered aspects of the role of THOC5 in signal transduction induced by extracellular stimuli. THOC5 is phosphorylated by several protein kinases at multiple residues upon extracellular stimuli. These include stimulation with growth factors/cytokines/chemokines, or DNA damage reagents. Furthermore, THOC5 is a substrate for several oncogenic tyrosine kinases, suggesting that THOC5 may be involved in cancer development. Recent THOC5 knockout mouse data reveal that THOC5 is an essential element in the maintenance of stem cells and growth factor/cytokine-mediated differentiation/proliferation. Furthermore, depletion of THOC5 influences less than 1% of total mRNA export in the steady state, however it influences more than 90% of growth factor/cytokine induced genes. THOC5, thereby contributes to the 3' processing and/or export of immediate-early genes induced by extracellular stimuli. These studies bring new insight into the link between the mRNA export complex and immediate-early gene response. The data from these studies also suggest that THOC5 may be a useful tool for studying stem cell biology, for modifying the differentiation processes and for cancer therapy.
细胞的生长、分化和向特定谱系的定向分化是由一组适时表达的生长因子/细胞因子受体及其下游转录因子基因所指导的。在分化过程中,基因表达的转录调控机制主要通过聚焦于启动子中的顺式和反式元件来研究,然而,mRNA 输出机制在分化过程中的作用尚未得到充分研究。THO(通过过度表达抑制 hpr1 delta 的转录缺陷)复合物 5(THOC5)是 THO 复合物的成员,THO 复合物是转录/输出复合物(TREX)的一个亚基。THOC5 在高等真核生物中是高度保守的,然而,THOC5 在转录和 mRNA 输出中的确切作用仍不清楚。在这篇综述中,我们重点介绍了 THOC5 在细胞外刺激诱导的信号转导中作用的最新发现。THOC5 在细胞外刺激下,在多个残基上被几种蛋白激酶磷酸化。这些刺激包括生长因子/细胞因子/趋化因子的刺激,或 DNA 损伤试剂的刺激。此外,THOC5 是几种致癌酪氨酸激酶的底物,这表明 THOC5 可能参与癌症的发展。最近的 THOC5 敲除小鼠数据表明,THOC5 是维持干细胞和生长因子/细胞因子介导的分化/增殖所必需的元素。此外,THOC5 的耗竭在稳态下影响不到 1%的总 mRNA 输出,但影响超过 90%的生长因子/细胞因子诱导的基因。THOC5 因此有助于细胞外刺激诱导的 3' 加工和/或输出。这些研究为 mRNA 输出复合物与早期基因反应之间的联系提供了新的见解。这些研究的数据还表明,THOC5 可能是研究干细胞生物学、修饰分化过程和癌症治疗的有用工具。