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SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex

机译:SOX9与人类甲状腺激素受体相关蛋白复合物的成分相互作用

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摘要

SOX9 transcription factor is involved in chondrocyte differentiation and male sex determination. Heterozygous defects in the human SOX9 gene cause campomelic dysplasia. The mechanisms behind SOX9 function are not understood despite the description of different target genes. This study therefore sets out to identify SOX9-associated proteins to unravel how SOX9 interacts with the cellular transcription machinery. We report the ability of SOX9 to interact with TRAP230, a component of the thyroid hormone receptor-associated protein (TRAP) complex. Both in vitro and in vivo assays have confirmed that the detected interaction is specific and occurs endogenously in cells. Using co-transfection experiments, we have also shown that the TRAP230 interacting domain can act in a dominant-negative manner regarding SOX9 activity. Our results add SOX9 to the list of activators that communicate with the general transcription machinery through the TRAP complex and suggest a basis for the collaboration of SOX9 with different coactivators that could contact the same coactivator/integrator complex.
机译:SOX9转录因子参与软骨细胞分化和男性性别的确定。人SOX9基因中的杂合缺陷会导致Campomic发育异常。尽管描述了不同的靶基因,但仍不了解SOX9功能背后的机制。因此,这项研究着手确定与SOX9相关的蛋白,以阐明SOX9与细胞转录机制如何相互作用。我们报告了SOX9与TRAP230相互作用的能力,TRAP230是甲状腺激素受体相关蛋白(TRAP)复合物的组成部分。体外和体内试验均已证实检测到的相互作用是特异性的,并且是细胞内源性发生的。使用共转染实验,我们还显示出TRAP230相互作用域在SOX9活性方面可以以显性负性方式起作用。我们的结果将SOX9添加到了通过TRAP复合物与通用转录机制进行通讯的激活物列表中,并为SOX9与可以接触同一共激活物/整合物复合物的不同共激活物的合作提供了基础。

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