A decoy receptor derived from alternative splicing fine-tunes cytokinin signaling in Arabidopsis.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-11-04 DOI:10.1016/j.molp.2024.11.001
Michaela Králová, Ivona Kubalová, Jakub Hajný, Karolina Kubiasová, Karolína Vagaská, Zengxiang Ge, Michelle Gallei, Hana Semerádová, Anna Kuchařová, Martin Hönig, Aline Monzer, Martin Kovačik, Jiří Friml, Ondřej Novák, Eva Benková, Yoshihisa Ikeda, David Zalabák
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Abstract

Hormone perception and signaling pathways play a fundamental regulatory function in the physiological processes of plants. Cytokinins, plant hormones, regulate cell division and meristem maintenance. The cytokinin signaling pathway is well-established in model plant Arabidopsis. Several negative feedback mechanisms, tightly controlling the cytokinin signaling output, were described previously. Here, we identified a new feedback mechanism executed through an alternative splicing of the cytokinin receptor AHK4/CRE1. A novel splicing variant named CRE1int7 results from seventh intron retention, introducing a premature termination codon in the transcript. We show that CRE1int7 is translated in planta into a truncated receptor lacking the C-terminal receiver domain essential for signal transduction. The CRE1int7 can bind the cytokinin but cannot activate the downstream cascade. We present a novel negative feedback mechanism of the cytokinin signaling pathway facilitated by a decoy receptor, which can inactivate canonical cytokinin receptors via dimerization and compete with them for ligand binding. While a similar molecular mechanism is well-known in mammals, decoy receptors are rare in plants. Ensuring proper plant growth and development requires precise control of the cytokinin signaling pathway at several levels. The CRE1int7 represents a yet unknown mechanism for fine-tuning the cytokinin signaling pathway in Arabidopsis.

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拟南芥中由替代剪接产生的诱饵受体可微调细胞分裂素信号。
激素感知和信号通路在植物的生理过程中发挥着基本的调节功能。细胞分裂素是一种植物激素,可调节细胞分裂和分生组织的维持。细胞分裂素信号通路在模式植物拟南芥中已经得到了很好的证实。以前曾描述过几种严格控制细胞分裂素信号输出的负反馈机制。在这里,我们发现了一种通过细胞分裂素受体 AHK4/CRE1 的替代剪接执行的新反馈机制。一种名为 CRE1int7 的新型剪接变体产生于第七个内含子的保留,在转录本中引入了一个过早终止密码子。我们发现,CRE1int7 在植物体内被翻译成一个截短的受体,缺乏信号转导所必需的 C 端接收结构域。CRE1int7 能与细胞分裂素结合,但不能激活下游级联。我们提出了一种由诱饵受体促进的新型细胞分裂素信号通路负反馈机制,诱饵受体可以通过二聚化使典型的细胞分裂素受体失活,并与之竞争配体结合。类似的分子机制在哺乳动物中广为人知,但诱饵受体在植物中却很少见。要确保植物的正常生长和发育,需要在多个水平上对细胞分裂素信号途径进行精确控制。CRE1int7 代表了拟南芥细胞分裂素信号途径微调的一种未知机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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