首页> 外文期刊>The Biochemical Journal >Protein intrinsic disorder in Arabidopsis NAC transcription factors: transcriptional activation by ANAC013 and ANAC046 and their interactions with RCD1
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Protein intrinsic disorder in Arabidopsis NAC transcription factors: transcriptional activation by ANAC013 and ANAC046 and their interactions with RCD1

机译:拟南芥NAC转录因子中的蛋白质内在病症:ANAC013和ANAC046的转录激活及其与RCD1的相互作用

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摘要

Protein ID (intrinsic disorder) plays a significant, yet relatively unexplored role in transcription factors (TFs). In the present paper, analysis of the transcription regulatory domains (TRDs) of six phylogenetically representative, plant-specific NAC [no apical meristem, ATAF (Arabidopsis transcription activation factor), cup-shaped cotyledon] TFs shows that the domains are present in similar average pre-molten or molten globule-like states, but have different patterns of order/disorder and MoRFs (molecular recognition features). ANAC046 (Arabidopsis NAC 046) was selected for further studies because of its simple MoRF pattern and its ability to interact with RCD1 (radical-induced cell death 1). Experiments in yeast and thermodynamic characterization suggest that its single MoRF region is sufficient for both transcriptional activation and interaction with RCD1. The remainder of the large regulatory domain is unlikely to contribute to the interaction, since the domain and truncations thereof have similar affinities for RCD1, which are also similar for ANAC013-RCD1 interactions. However, different enthalpic and entropic contributions to binding were revealed for ANAC046 and ANAC013, suggestive of differences in binding mechanisms. Although substitution of both hydrophobic and acidic residues of the ANAC046 MoRF region abolished binding, substitution of other residues, even with alpha-helix-breaking proline, was less disruptive. Together, the biophysical analyses suggest that RCD1-ANAC046 complex formation does not involve folding-upon-binding, but rather fuzziness or an unknown structure in ANAC046. We suggest that the ANAC046 regulatory domain functions as an entropic chain with a terminal hot spot interacting with RCD1. RCD1, a cellular hub, may be able to interact with many different TFs by exploiting their ID-based flexibility, as demonstrated for its interactions with ANAC046 and ANAC013.
机译:蛋白质ID(固有障碍)起着转录因子(TF)的一个显著,但相对未开发的作用。在本文件中,转录调节结构域的分析6个系统发育代表特定的植物NAC的(TRDS)[无顶端分生组织,ATAF(拟南芥转录激活因子),杯状子叶]转录因子表明结构域存在于相似平均预熔融或熔球样态,但具有有序/无序和MoRFs(分子识别特征)的不同的图案。 ANAC046(拟南芥NAC 046)被选择用于进一步的研究,因为它的简单MORF图案及其与RCD1(自由基诱导的细胞死亡1)相互作用的能力。在酵母和热力学性质的实验表明,其单MORF区域就足够实现转录激活,并与RCD1互动。在大的调节域的其余部分是不太可能有助于互动,因为域和截短形式有RCD1相似的亲和力,这也是ANAC013-RCD1相互作用相似。然而,不同的焓和结合,揭示了ANAC046和ANAC013熵的贡献,暗示在约束机制的差异。虽然ANAC046 MORF区域的疏水性和酸性残基的取代消除结合,其它残基的取代,甚至用α-螺旋破脯氨酸,较少的破坏性。在一起时,生物物理分析表明,RCD1-ANAC046复合物的形成不涉及折叠经结合,而是模糊性或ANAC046未知结构。我们建议ANAC046监管域中充当熵链与终端热点与RCD1交互。 RCD1,蜂窝毂,可能能够通过利用它们的基于ID的灵活性与许多不同的转录因子相互作用,这表现为与ANAC046和ANAC013相互作用。

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