Hernández-García Jorge, Carrillo-Carrasco Vanessa Polet, Rienstra Juriaan, Tanaka Keita, de Roij Martijn, Dipp-Álvarez Melissa, Freire-Ríos Alejandra, Crespo Isidro, Boer Roeland, van den Berg Willy A M, Lindhoud Simon, Weijers Dolf
Laboratory of Biochemistry, Wageningen University, Stippeneng 4, 6708WE, Wageningen, the Netherlands.
CAS Center for Excellence in Molecular Plant Sciences, 300 Feng Ling Road, Shanghai, 200032, PR China.
Nat Commun. 2024 Dec 30;15(1):10909. doi: 10.1038/s41467-024-55278-8.
The Auxin Response Factors (ARFs) family of transcription factors are the central mediators of auxin-triggered transcriptional regulation. Functionally different classes of extant ARFs operate as antagonistic auxin-dependent and -independent regulators. While part of the evolutionary trajectory to the present auxin response functions has been reconstructed, it is unclear how ARFs emerged, and how early diversification led to functionally different proteins. Here, we use in silico and in vivo analyses to revisit the molecular events that led to the origin and subsequent evolution of the ARFs. We reveal the shared origin of ARFs from preexisting domains, uncovering a protein fold homologous to the ARF DNA-binding fold in a conserved eukaryotic chromatin regulator. Building on this, we reconstruct the complete evolutionary history of ARFs, including the divergence events leading to the appearance of the ARF classes and defining the main molecular targets for their functional diversification. We derive a complete evolutionary trajectory that led to the emergence of the nuclear auxin signalling pathway.
生长素响应因子(ARFs)转录因子家族是生长素触发的转录调控的核心介质。现存功能不同类别的ARFs作为生长素依赖性和非依赖性调节因子发挥拮抗作用。虽然目前生长素响应功能的部分进化轨迹已经重建,但尚不清楚ARFs是如何出现的,以及早期的多样化如何导致功能不同的蛋白质。在这里,我们使用计算机模拟和体内分析来重新审视导致ARFs起源和后续进化的分子事件。我们揭示了ARFs起源于先前存在的结构域,在一种保守的真核染色质调节因子中发现了与ARF DNA结合折叠同源的蛋白质折叠。在此基础上,我们重建了ARFs的完整进化史,包括导致ARF类别出现的分歧事件,并确定了其功能多样化的主要分子靶点。我们得出了导致核生长素信号通路出现的完整进化轨迹。