Gould A, Morrison A, Sproat G, White R A, Krumlauf R
Laboratory of Developmental Neurobiology, Medical Research Council (MRC) National Institute for Medical Research, London, UK.
Genes Dev. 1997 Apr 1;11(7):900-13. doi: 10.1101/gad.11.7.900.
Vertebrate Hox genes display nested and overlapping patterns of expression. During mouse hindbrain development, Hoxb3 and Hoxb4 share an expression domain caudal to the boundary between rhombomeres 6 and 7. Transgenic analysis reveals that an enhancer (CR3) is shared between both genes and specifies this domain of overlap. Both the position of CR3 within the complex and its sequence are conserved from fish to mammals, suggesting it has a common role in regulating the vertebrate HoxB complex. CR3 mediates transcriptional activation by multiple Hox genes, including Hoxb4, Hoxd4, and Hoxb5 but not Hoxb1. It also functions as a selective HOX response element in Drosophila, where activation depends on Deformed, Sex combs reduced, and Antennapedia but not labial. Taken together, these data show that a Deformed/Hoxb4 autoregulatory loop has been conserved between mouse and Drosophila. In addition, these studies reveal the existence of positive cross-regulation and enhancer sharing as two mechanisms for reinforcing the overlapping expression domains of vertebrate Hox genes. In contrast, Drosophila Hox genes do not appear to share enhancers and where they overlap in expression, negative cross-regulatory interactions are observed. Therefore, despite many well documented aspects of Hox structural and functional conservation, there are mechanistic differences in Hox complex regulation between arthropods and vertebrates.
脊椎动物的Hox基因呈现出嵌套和重叠的表达模式。在小鼠后脑发育过程中,Hoxb3和Hoxb4在菱脑节6和7之间的边界尾侧共享一个表达域。转基因分析表明,这两个基因共享一个增强子(CR3),并指定了这个重叠域。CR3在复合体中的位置及其序列从鱼类到哺乳动物都是保守的,这表明它在调节脊椎动物HoxB复合体中具有共同作用。CR3介导多个Hox基因的转录激活,包括Hoxb4、Hoxd4和Hoxb5,但不包括Hoxb1。它在果蝇中也作为一种选择性的HOX反应元件发挥作用,其激活依赖于变形基因、小梳减少基因和触角足基因,而不依赖于唇基因。综上所述,这些数据表明,在小鼠和果蝇之间,变形基因/Hoxb4自调控环是保守的。此外,这些研究揭示了正向交叉调节和增强子共享的存在,这是加强脊椎动物Hox基因重叠表达域的两种机制。相比之下,果蝇的Hox基因似乎不共享增强子,在它们表达重叠的地方,观察到负向交叉调节相互作用。因此,尽管Hox结构和功能保守有许多已充分记录的方面,但节肢动物和脊椎动物在Hox复合体调控方面存在机制差异。