Giraldez F
Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladollid-CSIC, Facultad de Medicina, Valladolid, 47005, Spain.
Dev Biol. 1998 Nov 1;203(1):189-200. doi: 10.1006/dbio.1998.9023.
LIM homeodomain genes have been involved in patterning in a variety of organisms. I have analyzed the expression of lmx1 during early ear development and explored its regulation by the neuroectoderm. Experiments were carried out on chick embryos. During early somitic stages (4-6 somites), lmx1 was expressed in the neural tube and in a stripe of the dorsal ectoderm. The ectodermal expression domain was then restricted to the otic placode (7-10 somites). At otic cup stages, lmx1 was downregulated in ventral and medial aspects of the otic epithelium facing the neural tube. This resulted in a dorsal and lateral restriction of lmx1 that persisted until the otic vesicle stage. The dependence of lmx1 on interactions with the neuroectoderm was explored by carrying out ablations of the neural tube in organotypic explants containing the otic presumptive ectoderm. Both the formation of the otic vesicle and expression of lmx1 were dependent on the presence of the neural ectoderm during stages preceding placode formation (4-6 somites). Thereafter, the formation of the otic vesicle was progressively autonomous, and by the stage of 10 somites the otic ectoderm developed into otic vesicles and expressed lmx1 in foreign environments. Dorsal and ventral neuroectoderms displayed differential effects on lmx1 expression. Ablation of the dorsal neural tube resulted in a reduced expression of lmx1, which was more dramatic during early placode and preplacode stages (5-7 somites). Removal of the ventral aspect of the neural tube (including the notochord) had opposite effects, expression of lmx1 increased, and its domain expanded. The formation of the otic vesicle, however, was supported by either the dorsal or ventral neuroectoderm. The experiments suggest that lmx1 is involved in early patterning of the otic vesicle, and they provide evidence for the regional segregation of organizing activities within the neural tube.
LIM 同源异型域基因参与了多种生物体的模式形成。我分析了 lmx1 在耳早期发育过程中的表达,并探讨了神经外胚层对其的调控。实验在鸡胚上进行。在早期体节阶段(4 - 6 体节),lmx1 在神经管和背侧外胚层的一条带中表达。然后外胚层表达区域局限于耳基板(7 - 10 体节)。在耳杯阶段,lmx1 在面向神经管的耳上皮的腹侧和内侧下调。这导致 lmx1 在背侧和外侧受到限制,这种限制一直持续到耳泡阶段。通过在含有耳原基外胚层的器官型外植体中切除神经管,探讨了 lmx1 对与神经外胚层相互作用的依赖性。在基板形成前的阶段(4 - 6 体节),耳泡的形成和 lmx1 的表达都依赖于神经外胚层的存在。此后,耳泡的形成逐渐自主,到 10 体节阶段,耳外胚层在外部环境中发育成耳泡并表达 lmx1。背侧和腹侧神经外胚层对 lmx1 表达表现出不同的影响。切除背侧神经管导致 lmx1 表达降低,在早期基板和前基板阶段(5 - 7 体节)更为明显。切除神经管的腹侧部分(包括脊索)则产生相反的效果,lmx1 的表达增加,其区域扩大。然而,耳泡的形成由背侧或腹侧神经外胚层支持。这些实验表明 lmx1 参与了耳泡的早期模式形成,并为神经管内组织活性的区域分离提供了证据。