Sham M H, Vesque C, Nonchev S, Marshall H, Frain M, Gupta R D, Whiting J, Wilkinson D, Charnay P, Krumlauf R
MRC Laboratory of Eukaryotic Molecular Genetics, National Institute for Medical Research, The Ridgeway, Mill Hill, London.
Cell. 1993 Jan 29;72(2):183-96. doi: 10.1016/0092-8674(93)90659-e.
The zinc finger gene Krox20 and many Hox homeobox genes are expressed in segment-restricted domains in the hindbrain. The restricted expression patterns appear before morphological segmentation, suggesting that these transcription factors may play an early role in the establishment and identity of rhombomeric segments. In this paper, we show that the HoxB2 (Hox2.8) gene is normally upregulated in rhombomeres (r) 3, 4, and 5, and we identify an enhancer region upstream of the gene that imposes r3/r5 expression in transgenic mice. This enhancer contains three Krox20-binding sites required in vitro for complex formation with Krox20 protein and in vivo for rhombomere-restricted expression. In transgenic mice, Krox20 expressed in ectopic domains can transactivate a reporter construct containing the HoxB2 r3/r5 enhancer. These data demonstrate that Krox20 is a part of the upstream transcriptional cascade that directly regulates HoxB2 expression during hindbrain segmentation.
锌指基因Krox20和许多Hox同源框基因在后脑的节段限制性区域表达。这种限制性表达模式在形态学分割之前就出现了,这表明这些转录因子可能在菱脑节段的建立和特征形成中发挥早期作用。在本文中,我们表明HoxB2(Hox2.8)基因通常在菱脑节(r)3、4和5中上调,并且我们鉴定出该基因上游的一个增强子区域,该区域在转基因小鼠中赋予r3/r5表达。这个增强子包含三个Krox20结合位点,在体外这些位点对于与Krox20蛋白形成复合物是必需的,在体内对于菱脑节限制性表达是必需的。在转基因小鼠中,在异位区域表达的Krox20可以反式激活包含HoxB2 r3/r5增强子的报告基因构建体。这些数据表明Krox20是上游转录级联反应的一部分,该级联反应在菱脑分割过程中直接调节HoxB2的表达。