Singh Rajeev, Lauth Matthias
Philipps University Marburg, Institute of Molecular Biology and Tumor Research (IMT), Center for Tumor and Immune Biology (ZTI), Hans-Meerwein-Str. 3, 35043 Marburg, Germany.
J Dev Biol. 2017 Nov 21;5(4):13. doi: 10.3390/jdb5040013.
Hedgehog (Hh)/GLI signaling is an important instructive cue in various processes during embryonic development, such as tissue patterning, stem cell maintenance, and cell differentiation. It also plays crucial roles in the development of many pediatric and adult malignancies. Understanding the molecular mechanisms of pathway regulation is therefore of high interest. Dual-specificity tyrosine phosphorylation-regulated kinases (DYRKs) comprise a group of protein kinases which are emerging modulators of signal transduction, cell proliferation, survival, and cell differentiation. Work from the last years has identified a close regulatory connection between DYRKs and the Hh signaling system. In this manuscript, we outline the mechanistic influence of DYRK kinases on Hh signaling with a focus on the mammalian situation. We furthermore aim to bring together what is known about the functional consequences of a DYRK-Hh cross-talk and how this might affect cellular processes in development, physiology, and pathology.
刺猬索尼克(Hh)/GLI信号通路是胚胎发育过程中各种进程的重要指导信号,如组织模式形成、干细胞维持和细胞分化。它在许多儿童和成人恶性肿瘤的发生发展中也起着关键作用。因此,了解该信号通路调控的分子机制具有重要意义。双特异性酪氨酸磷酸化调节激酶(DYRKs)是一组蛋白激酶,它们逐渐成为信号转导、细胞增殖、存活和细胞分化的调节因子。过去几年的研究发现了DYRKs与Hh信号系统之间紧密的调控联系。在本手稿中,我们概述了DYRK激酶对Hh信号通路的机制性影响,重点关注哺乳动物的情况。此外,我们旨在汇总关于DYRK-Hh相互作用的功能后果以及这可能如何影响发育、生理和病理过程中的细胞进程的已知信息。