Garriga-Canut Mireia, Orkin Stuart H
Division of Hematology/Oncology, Children's Hospital and Dana Farber Cancer Institute, Harvard Medical School and Howard Hughes Medical Institute, Boston, Massachusetts 02115, USA.
J Biol Chem. 2004 May 28;279(22):23597-605. doi: 10.1074/jbc.M313987200. Epub 2004 Mar 22.
Physical association between the transcription factor GATA-1 and the cofactor, Friend of GATA-1 (FOG-1), is essential for the differentiation of two blood cell types, erythroid cells and megakaryocytes. However, little is known regarding the mechanisms that modulate their interaction within cells. In the present study, we have identified TACC3 as a FOG-1-interacting protein. Transforming acidic coiled-coil protein 3 (TACC3), a protein that is highly expressed in hematopoietic cells, has been reported to have a critical role in the expansion of immature hematopoietic progenitors. We show that TACC3 affects FOG-1 nuclear localization, altering the interaction between GATA-1 and FOG-1. However, GATA-1 competes with TACC3 in the interaction with FOG-1. We observe that high levels of TACC3 inhibit the function of FOG-1 as a transcriptional cofactor of GATA-1. Furthermore, forced expression of TACC3 to levels similar to those found in progenitor cells delays terminal maturation of MEL and G1ER cells, two cell models of erythroid cell development. We suggest a role for TACC3 in regulating the cellular distribution of FOG-1 and thus the direct interaction of GATA-1 and FOG-1 as a mechanism to control the transition between expansion of multipotential progenitor cell populations and final stages of erythroid maturation.
转录因子GATA-1与辅因子GATA-1之友(FOG-1)之间的物理关联对于两种血细胞类型(红细胞和巨核细胞)的分化至关重要。然而,关于调节它们在细胞内相互作用的机制却知之甚少。在本研究中,我们鉴定出TACC3是一种与FOG-1相互作用的蛋白。转化酸性卷曲螺旋蛋白3(TACC3)是一种在造血细胞中高度表达的蛋白,据报道它在未成熟造血祖细胞的扩增中起关键作用。我们发现TACC3影响FOG-1的核定位,改变GATA-1与FOG-1之间的相互作用。然而,GATA-1在与FOG-1的相互作用中与TACC3竞争。我们观察到高水平的TACC3抑制FOG-1作为GATA-1转录辅因子的功能。此外,将TACC3强制表达至与祖细胞中相似的水平会延迟MEL和G1ER细胞(红细胞发育的两种细胞模型)的终末成熟。我们认为TACC3在调节FOG-1的细胞分布以及GATA-1与FOG-1的直接相互作用中发挥作用,以此作为控制多能祖细胞群体扩增与红细胞成熟终末阶段之间转变的一种机制。