Jeong Yongsu, El-Jaick Kenia, Roessler Erich, Muenke Maximilian, Epstein Douglas J
Department of Genetics, University of Pennsylvania School of Medicine, Clinical Research Building, Room 470, 415 Curie Boulevard, Philadelphia, PA 19104, USA.
Development. 2006 Feb;133(4):761-72. doi: 10.1242/dev.02239. Epub 2006 Jan 11.
The secreted protein sonic hedgehog (Shh) plays an integral role in forming the ventral midline of the vertebrate central nervous system (CNS). In the absence of Shh function, ventral midline development is perturbed resulting in holoprosencephaly (HPE), a structural malformation of the brain, as well as in neuronal patterning and path finding defects along the length of the anteroposterior neuraxis. Central to the understanding of ventral neural tube development is how Shh transcription is regulated in the CNS. To address this issue, we devised an enhancer trap assay to systematically screen 1 Mb of DNA surrounding the Shh locus for the ability to target reporter gene expression to sites of Shh transcription in transgenic mouse embryos. This analysis uncovered six enhancers distributed over 400 kb, the combined activity of which covered all sites of Shh expression in the mouse embryonic CNS from the ventral forebrain to the posterior extent of the spinal cord. To evaluate the relative contribution of these enhancers to the overall pattern of Shh expression, individual elements were deleted in the context of a transgenic Bac reporter assay. Redundant mechanisms were found to control Shh-like reporter activity in the ventral spinal cord, hindbrain and regions of the telencephalon, whereas unique elements regulated Shh-like expression in the ventral midbrain, the majority of the ventral diencephalon and parts of the telencephalon. Three ventral forebrain enhancers locate on the distal side of translocation breakpoints that occurred upstream of Shh in human cases of HPE, suggesting that displacement of these regulatory elements from the Shh promoter is a likely cause of HPE in these individuals.
分泌蛋白音猬因子(Shh)在脊椎动物中枢神经系统(CNS)腹侧中线的形成过程中发挥着不可或缺的作用。在缺乏Shh功能的情况下,腹侧中线发育会受到干扰,导致全前脑畸形(HPE),这是一种脑部结构畸形,同时还会出现沿前后神经轴长度的神经元模式形成和路径寻找缺陷。理解腹侧神经管发育的核心在于了解Shh转录在中枢神经系统中是如何被调控的。为了解决这个问题,我们设计了一种增强子捕获分析方法,系统地筛选围绕Shh基因座的1兆碱基DNA,以确定其在转基因小鼠胚胎中将报告基因表达靶向Shh转录位点的能力。该分析发现了分布在400千碱基上的六个增强子,它们的联合活性覆盖了从小鼠胚胎中枢神经系统腹侧前脑到脊髓后部的所有Shh表达位点。为了评估这些增强子对Shh表达整体模式的相对贡献,在转基因细菌人工染色体(Bac)报告分析的背景下删除了各个元件。结果发现存在冗余机制控制脊髓腹侧、后脑和端脑区域的Shh样报告基因活性,而独特的元件调控中脑腹侧、大部分间脑腹侧和部分端脑的Shh样表达。在人类HPE病例中,三个腹侧前脑增强子位于Shh上游发生的易位断点的远端,这表明这些调控元件从Shh启动子的移位可能是这些个体发生HPE的原因。