Paxton Christian N, Bleyl Steven B, Chapman Susan C, Schoenwolf Gary C
University of Utah, Dept. of Neurobiology and Anatomy, Salt Lake City, UT 84132-3401, USA.
Gene Expr Patterns. 2010 Jan;10(1):31-43. doi: 10.1016/j.gep.2009.11.002. Epub 2009 Nov 11.
To understand the etiology of congenital hearing loss, a comprehensive understanding of the molecular genetic mechanisms underlying normal ear development is required. We are identifying genes involved in otogenesis, with the longer term goal of studying their mechanisms of action, leading to inner ear induction and patterning. Using Agilent microarrays, we compared the differential expression of a test domain (which consisted of the pre-otic placodal ectoderm with the adjacent hindbrain ectoderm and the underlying mesendodermal tissues) with a rostral control domain (which included tissue that is competent, but not specified, to express inner ear markers in explant assays). We identified 1261 transcripts differentially expressed between the two domains at a 2-fold or greater change: 463 were upregulated and 798 were downregulated in the test domain. We validated the differential expression of several signaling molecules and transcription factors identified in this array using in situ hybridization. Furthermore, the expression patterns of the validated group of genes from the test domain were explored in detail to determine how the timing of their expression relates to specific events of otic induction and development. In conclusion, we identified a number of novel candidate genes for otic placode induction.
为了解先天性听力损失的病因,需要全面了解正常耳发育背后的分子遗传机制。我们正在鉴定参与耳发生的基因,其长期目标是研究它们的作用机制,从而实现内耳诱导和模式形成。使用安捷伦微阵列,我们将一个测试区域(由耳前基板外胚层与相邻的后脑外胚层以及下方的中内胚层组织组成)与一个头端对照区域(包括在体外实验中能够表达内耳标志物但未被指定表达的组织)的差异表达进行了比较。我们鉴定出在两个区域之间差异表达2倍或更大倍数变化的1261个转录本:在测试区域中,463个上调,798个下调。我们使用原位杂交验证了该阵列中鉴定出的几种信号分子和转录因子的差异表达。此外,详细探究了测试区域中经过验证的一组基因的表达模式,以确定它们的表达时间与耳诱导和发育的特定事件之间的关系。总之,我们鉴定出了一些用于耳基板诱导的新候选基因。