Chitnis A, Kintner C
The Salk Institute for Biological Studies, San Diego, CA 92186-5800, USA.
Development. 1996 Jul;122(7):2295-301. doi: 10.1242/dev.122.7.2295.
We have compared the roles of XASH-3 and NeuroD, two basic helix-loop-helix transcription factors, in the formation of primary neurons in early Xenopus embryos. When ectopically expressed in Xenopus embryos, XASH-3 and NeuroD induce ectopic primary neurons in very different spatial patterns. We show that the pattern of primary neurons induced by XASH-3 and NeuroD can be accounted for by a difference in their sensitivity to inhibitory interactions mediated by the neurogenic genes, X-Delta-1 and X-Notch-1. Both NeuroD and XASH-3 promote the expression of the inhibitory ligand, X-Delta-1. However, XASH-3 appears to be sensitive to the inhibitory effects of X-Delta-1 while NeuroD is much less so. Consequently only a subset of cells that ectopically express XASH-3 eventually form neurons, giving a scattered pattern, while the ectopic expression of NeuroD leads to a relatively dense pattern of ectopic neurons. We propose that differences in the sensitivity of XASH-3 and NeuroD to lateral inhibition play an important role during their respective roles in neuronal determination and differentiation.
我们比较了两种碱性螺旋-环-螺旋转录因子XASH-3和NeuroD在非洲爪蟾早期胚胎原代神经元形成过程中的作用。当在非洲爪蟾胚胎中异位表达时,XASH-3和NeuroD以非常不同的空间模式诱导异位原代神经元。我们发现,XASH-3和NeuroD诱导的原代神经元模式可以通过它们对由神经源基因X-Delta-1和X-Notch-1介导的抑制性相互作用的敏感性差异来解释。NeuroD和XASH-3都促进抑制性配体X-Delta-1的表达。然而,XASH-3似乎对X-Delta-1的抑制作用敏感,而NeuroD则不太敏感。因此,只有一部分异位表达XASH-3的细胞最终形成神经元,形成分散的模式,而异位表达NeuroD则导致异位神经元相对密集的模式。我们提出,XASH-3和NeuroD对侧向抑制的敏感性差异在它们各自在神经元决定和分化中的作用中起着重要作用。