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intervening 结构域是植物 MADS 转录因子结合 DNA 和发挥功能所必需的。

The intervening domain is required for DNA-binding and functional identity of plant MADS transcription factors.

机构信息

Laboratoire Physiologie Cellulaire et Végétale, Université Grenoble Alpes, CNRS, CEA, INRAE, IRIG-DBSCI-LPCV, Grenoble, France.

Plant Cell and Molecular Biology, Institute of Biology, Humboldt-Universität zu Berlin, Berlin, Germany.

出版信息

Nat Commun. 2021 Aug 6;12(1):4760. doi: 10.1038/s41467-021-24978-w.

Abstract

The MADS transcription factors (TF) are an ancient eukaryotic protein family. In plants, the family is divided into two main lineages. Here, we demonstrate that DNA binding in both lineages absolutely requires a short amino acid sequence C-terminal to the MADS domain (M domain) called the Intervening domain (I domain) that was previously defined only in type II lineage MADS. Structural elucidation of the MI domains from the floral regulator, SEPALLATA3 (SEP3), shows a conserved fold with the I domain acting to stabilise the M domain. Using the floral organ identity MADS TFs, SEP3, APETALA1 (AP1) and AGAMOUS (AG), domain swapping demonstrate that the I domain alters genome-wide DNA-binding specificity and dimerisation specificity. Introducing AG carrying the I domain of AP1 in the Arabidopsis ap1 mutant resulted in strong complementation and restoration of first and second whorl organs. Taken together, these data demonstrate that the I domain acts as an integral part of the DNA-binding domain and significantly contributes to the functional identity of the MADS TF.

摘要

MADS 转录因子(TF)是一种古老的真核蛋白家族。在植物中,该家族分为两个主要谱系。在这里,我们证明,两个谱系的 DNA 结合都绝对需要 MADS 结构域(M 结构域)C 端的一个短氨基酸序列,称为介入结构域(I 结构域),该结构域以前仅在 II 谱系 MADS 中定义。来自花调控因子 SEPALLATA3(SEP3)的 MI 结构域的结构阐明表明,存在一个保守的折叠,I 结构域起到稳定 M 结构域的作用。使用花器官身份 MADS TF,SEP3、APETALA1(AP1)和 AGAMOUS(AG),结构域交换表明 I 结构域改变了全基因组 DNA 结合特异性和二聚体特异性。在拟南芥 ap1 突变体中引入携带 AP1 I 结构域的 AG,导致第一和第二轮器官的强烈互补和恢复。总之,这些数据表明 I 结构域作为 DNA 结合结构域的一个组成部分,对 MADS TF 的功能特性有重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce9/8346517/d07f84af5e9e/41467_2021_24978_Fig1_HTML.jpg

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