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障碍:由ANAC013和ANAC046进行的转录激活及其与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(本征性疾病)在转录因子(TF)中起着重要但相对未开发的作用。在本文中,对六个系统发生学上具有代表性的植物特异性NAC [无顶端分生组织,ATAF(拟南芥转录激活因子),杯状子叶] TFs的转录调控域(TRD)的分析显示,这些域存在于相似的区域平均熔融前或熔融小球状状态,但具有不同的有序/无序和MoRF(分子识别特征)模式。选择ANAC046(拟南芥NAC 046)进行进一步研究,是因为其简单的MoRF模式及其与RCD1相互作用的能力(自由基诱导的细胞死亡1)。酵母和热力学表征实验表明,其单个MoRF区足以实现转录激活和与RCD1的相互作用。大调节域的其余部分不太可能对相互作用有所贡献,因为其域和其截短部分对RCD1具有相似的亲和力,对于ANAC013-RCD1相互作用也具有相似的亲和力。但是,对于ANAC046和ANAC013揭示了不同的焓和熵对结合的贡献,表明了结合机制的差异。尽管ANAC046 MoRF区的疏水残基和酸性残基的取代均消除了结合,但其他残基的取代,即使被破坏α-螺旋的脯氨酸,破坏性也较小。总之,生物物理分析表明,RCD1-ANAC046复合物的形成不涉及结合时折叠,而是涉及ANAC046中的模糊性或未知结构。我们建议,ANAC046调节域起熵链的作用,其末端热点与RCD1相互作用。 RCD1是一个蜂窝集线器,它可以利用基于ID的灵活性来与许多不同的TF进行交互,如其与ANAC046和ANAC013的交互所证明的。

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