Grunfeld Noam, Levine Erel, Libby Elizabeth
Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA.
Department of Chemical Engineering, Northeastern University, Boston, Massachusetts, USA.
Mol Microbiol. 2024 Aug;122(2):152-164. doi: 10.1111/mmi.15220. Epub 2024 Jan 3.
Bacteria possess diverse classes of signaling systems that they use to sense and respond to their environments and execute properly timed developmental transitions. One widespread and evolutionarily ancient class of signaling systems are the Hanks-type Ser/Thr kinases, also sometimes termed "eukaryotic-like" due to their homology with eukaryotic kinases. In diverse bacterial species, these signaling systems function as critical regulators of general cellular processes such as metabolism, growth and division, developmental transitions such as sporulation, biofilm formation, and virulence, as well as antibiotic tolerance. This multifaceted regulation is due to the ability of a single Hanks-type Ser/Thr kinase to post-translationally modify the activity of multiple proteins, resulting in the coordinated regulation of diverse cellular pathways. However, in part due to their deep integration with cellular physiology, to date, we have a relatively limited understanding of the timing, regulatory hierarchy, the complete list of targets of a given kinase, as well as the potential regulatory overlap between the often multiple kinases present in a single organism. In this review, we discuss experimental methods and curated datasets aimed at elucidating the targets of these signaling pathways and approaches for using these datasets to develop computational models for quantitative predictions of target motifs. We emphasize novel approaches and opportunities for collecting data suitable for the creation of new predictive computational models applicable to diverse species.
细菌拥有多种信号系统,它们利用这些系统感知并响应环境,以及适时地进行发育转变。一类广泛存在且在进化上古老的信号系统是汉克斯型丝氨酸/苏氨酸激酶,由于它们与真核激酶具有同源性,有时也被称为“类真核”激酶。在多种细菌物种中,这些信号系统作为一般细胞过程(如代谢、生长和分裂)、发育转变(如孢子形成、生物膜形成和毒力)以及抗生素耐受性的关键调节因子发挥作用。这种多方面的调节归因于单个汉克斯型丝氨酸/苏氨酸激酶能够在翻译后修饰多种蛋白质的活性,从而导致对多种细胞途径的协同调节。然而,部分由于它们与细胞生理学的深度整合,迄今为止,我们对给定激酶的作用时间、调节层次、完整的靶标列表以及单个生物体中通常存在的多种激酶之间潜在的调节重叠的了解相对有限。在这篇综述中,我们讨论了旨在阐明这些信号通路靶标的实验方法和经过整理的数据集,以及利用这些数据集开发用于定量预测靶标基序的计算模型的方法。我们强调了收集适合创建适用于多种物种的新预测计算模型的数据的新方法和机会。