Dijkmans Thomas Frederik, van Hooijdonk Leonarda Wilhelmina Antonia, Fitzsimons Carlos Patrick, Vreugdenhil Erno
Leiden/Amsterdam Center for Drug Research and Leiden University Medical Center, The Netherlands.
Cent Nerv Syst Agents Med Chem. 2010 Mar;10(1):32-46. doi: 10.2174/187152410790780118.
The doublecortin gene family is associated with subcortical band heterotopia, lissencephaly, epilepsy, developmental dyslexia and retinitis pigmentosa. At least 11 genes homologous to the doublecortin gene exist in humans and mice. Cellular processes regulated by different members of the doublecortin family involve neuronal migration, neurogenesis and eye receptor development. Underlying mechanisms include regulation of cytoskeletal structure and microtubule-based transport. Through their doublecortin-domains, doublecortin proteins can bind microtubules and regulate microtubule-dependent processes. However, this regulation is complex and involves many interacting proteins. Moreover, different spatiotemporal expression patterns and the generation of splice variants further contribute to this complexity. The doublecortin-like kinase 1 gene in particular, produces splice variants with different protein domains such as doublecortin-domains, a serine, threonine and proline-rich domain and a serine/threonine kinase-domain. Here, we review our current knowledge on the doublecortin gene family with an emphasis on proteins interacting with doublecortin domains and other domains. In addition, to generate new hypotheses for further research, we analyzed the serine, threonine and proline-rich domain for predicted protein interactions.
双皮质素基因家族与皮质下带状异位、无脑回畸形、癫痫、发育性阅读障碍和色素性视网膜炎相关。在人类和小鼠中存在至少11个与双皮质素基因同源的基因。双皮质素家族不同成员所调控的细胞过程涉及神经元迁移、神经发生和眼受体发育。潜在机制包括细胞骨架结构的调控和基于微管的运输。通过其双皮质素结构域,双皮质素蛋白可以结合微管并调节依赖微管的过程。然而,这种调节是复杂的,涉及许多相互作用的蛋白质。此外,不同的时空表达模式和剪接变体的产生进一步加剧了这种复杂性。特别是双皮质素样激酶1基因,产生具有不同蛋白质结构域的剪接变体,如双皮质素结构域、富含丝氨酸、苏氨酸和脯氨酸的结构域以及丝氨酸/苏氨酸激酶结构域。在这里,我们综述了目前关于双皮质素基因家族的知识,重点关注与双皮质素结构域和其他结构域相互作用的蛋白质。此外,为了产生进一步研究的新假设,我们分析了富含丝氨酸、苏氨酸和脯氨酸的结构域以预测蛋白质相互作用。