Dept. of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208, USA.
Int J Biochem Cell Biol. 2010 Mar;42(3):441-4. doi: 10.1016/j.biocel.2009.11.014. Epub 2009 Nov 30.
Neural crest cells are the primary innovation that led to evolution of the vertebrates, and transcription factors of the SoxE family (Sox8, Sox9 and Sox10) are among the central players regulating the development of these cells. In all vertebrates examined to date, one or more SoxE proteins are required for the formation of neural crest cells, the maintenance of their multipotency, and their survival. Later, SoxE proteins drive the formation of multiple neural crest derivatives including chondrocytes, melanocytes, and cells of the peripheral nervous system, particularly Schwann cells/peripheral glia. Given their multiple diverse roles in the development of the neural crest, it is important to understand how the activity of SoxE factors is controlled such that they direct the correct developmental outcome. While combinatorial control with other regulatory factors is clearly one mechanism for generating such functional versatility, modulation of SoxE activity, both by SoxD family factors and by post-translational modification, also appears to be important. Elucidating the mechanisms that control SoxE function is essential to understand the evolutionary origin of the vertebrates, as well as a host of SoxE-linked syndromes and diseases, and may prove crucial for developing stem cell based therapies that target SoxE-regulated cell types.
神经嵴细胞是导致脊椎动物进化的主要创新,SoxE 家族的转录因子(Sox8、Sox9 和 Sox10)是调节这些细胞发育的核心参与者之一。在迄今为止检查的所有脊椎动物中,一个或多个 SoxE 蛋白对于神经嵴细胞的形成、其多能性的维持以及它们的存活都是必需的。后来,SoxE 蛋白驱动多种神经嵴衍生物的形成,包括软骨细胞、黑色素细胞和周围神经系统的细胞,特别是施万细胞/周围神经胶质。鉴于它们在神经嵴发育中的多种不同作用,了解 SoxE 因子的活性是如何被控制的,从而指导正确的发育结果,这一点很重要。虽然与其他调节因子的组合控制显然是产生这种多功能性的一种机制,但 SoxD 家族因子和翻译后修饰对 SoxE 活性的调节似乎也很重要。阐明控制 SoxE 功能的机制对于理解脊椎动物的进化起源以及许多与 SoxE 相关的综合征和疾病至关重要,并且可能对于开发针对 SoxE 调节的细胞类型的基于干细胞的治疗方法至关重要。