LaBonne C, Bronner-Fraser M
Division of Biology 139-74, California Institute of Technology, Pasadena, California 91125, USA.
Dev Biol. 2000 May 1;221(1):195-205. doi: 10.1006/dbio.2000.9609.
The neural crest is a transient population of precursor cells that arises at the border between the neural plate and prospective epidermis in vertebrate embryos. The earliest known response to neural-crest-inducing signals is the expression of the zinc-finger transcription factors slug and snail. Although it is widely believed that these transcription factors play an essential role in neural crest development, relatively little is understood about their mechanism of action during this process. We have previously shown that overexpression of XSlug leads to expanded expression of neural crest markers and an excess of at least one neural crest derivative, melanocytes. In order to further investigate XSlug function, we overexpressed mutant constructs in which the DNA-binding domain was fused to either the activation domain from Gal4 or the repressor domain from Drosophila Engrailed. The Engrailed repressor fusion was found to mimic the effects of wild-type XSlug, indicating that XSlug functions as a transcriptional repressor during neural crest formation. In contrast, overexpression of either the activation domain fusion or the DNA-binding domain alone was found to inhibit XSlug function. Using a hormone-inducible inhibitory mutant, we show that inhibition of XSlug function at early stages prevents the formation of neural crest precursors, while inhibition at later stages interferes with neural crest migration, demonstrating for the first time that this transcriptional repressor is required during multiple stages of neural crest development.
神经嵴是脊椎动物胚胎中出现在神经板和预期表皮边界处的一群短暂存在的前体细胞。已知对神经嵴诱导信号的最早反应是锌指转录因子Slug和Snail的表达。尽管人们普遍认为这些转录因子在神经嵴发育中起重要作用,但对它们在此过程中的作用机制了解相对较少。我们之前已经表明,XSlug的过表达会导致神经嵴标志物的表达扩展以及至少一种神经嵴衍生物黑素细胞的过量产生。为了进一步研究XSlug的功能,我们过表达了突变构建体,其中DNA结合结构域与来自Gal4的激活结构域或来自果蝇Engrailed的抑制结构域融合。发现Engrailed抑制融合体模拟了野生型XSlug的作用,表明XSlug在神经嵴形成过程中作为转录抑制因子发挥作用。相比之下,发现激活结构域融合体或单独的DNA结合结构域的过表达会抑制XSlug的功能。使用激素诱导型抑制突变体,我们表明在早期阶段抑制XSlug功能会阻止神经嵴前体细胞的形成,而在后期阶段抑制则会干扰神经嵴的迁移,首次证明这种转录抑制因子在神经嵴发育的多个阶段都是必需的。