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拟滞蛋白与多步磷酸传递中介物组氨酸磷酸转移酶在藓类植物Physcomitrium patens 中的核相互作用。

Nuclear interactions between the Pseudo-Response Regulator clock proteins and the Multi-Step Phosphorelay mediator Histidine-containing phosphotransfers in the moss Physcomitrium patens.

机构信息

Graduate School of Informatics, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan.

Graduate School of Bioagriculture, Nagoya University, Furo- Cho, Chikusa-ku, Nagoya, 464-8601, Japan.

出版信息

Biochem Biophys Res Commun. 2024 Nov 12;733:150734. doi: 10.1016/j.bbrc.2024.150734. Epub 2024 Sep 21.

Abstract

Pseudo-Response Regulator (PRR) proteins constitute a fundamental set of circadian clock components in plants. PRRs have an amino acid sequence stretch with similarity to the receiver (REC) domain of response regulators (RRs) in the Multi-Step Phosphorelay (MSP). However, it has never been elucidated whether PRRs interact with Histidine-containing Phosphotransfer (HPt) proteins, which transfer a phosphate to RRs. Here, we studied whether PRRs interact with HPts in the moss Physcomitrium patens by the Yeast Two-Hybrid system and Bimolecular Fluorescence Complementation. P. patens PRR1/2/3 interacted with HPt1/2 in the nucleus, but not with HPt3, suggesting that P. patens PRRs function as authentic RRs. We discuss these results in relation to the evolution and diversity of the plant circadian clocks.

摘要

拟应答调节蛋白(PRR)构成了植物生物钟的基本组成部分。PRR 蛋白具有与多步磷酸传递(MSP)中响应调节蛋白(RR)的受体(REC)结构域相似的氨基酸序列延伸。然而,PRR 是否与将磷酸基团转移到 RR 的组氨酸磷酸转移(HPt)蛋白相互作用,这一点尚未阐明。在这里,我们通过酵母双杂交系统和双分子荧光互补研究了苔藓Physcomitrium patens 中 PRR 与 HPt 的相互作用。Physcomitrium patens PRR1/2/3 在核内与 HPt1/2 相互作用,但不与 HPt3 相互作用,表明 Physcomitrium patens PRR 作为真正的 RR 发挥作用。我们将这些结果与植物生物钟的进化和多样性联系起来进行讨论。

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