Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Korea.
PLoS One. 2012;7(7):e40735. doi: 10.1371/journal.pone.0040735. Epub 2012 Jul 12.
The mammalian cochlear duct is tonotopically organized such that the basal cochlea is tuned to high frequency sounds and the apical cochlea to low frequency sounds. In an effort to understand how this tonotopic organization is established, we searched for genes that are differentially expressed along the tonotopic axis during neonatal development. Cochlear tissues dissected from P0 and P8 mice were divided into three equal pieces, representing the base, middle and apex, and gene expression profiles were determined using the microarray technique. The gene expression profiles were grouped according to changes in expression levels along the tonotopic axis as well as changes during neonatal development. The classified groups were further analyzed by functional annotation clustering analysis to determine whether genes associated with specific biological function or processes are particularly enriched in each group. These analyses identified several candidate genes that may be involved in cochlear development and acquisition of tonotopy. We examined the expression domains for a few candidate genes in the developing mouse cochlea. Tnc (tenacin C) and Nov (nephroblastoma overexpressed gene) are expressed in the basilar membrane, with increased expression toward the apex, which may contribute to graded changes in the structure of the basilar membrane along the tonotopic axis. In addition, Fst (Follistatin), an antagonist of TGF-β/BMP signaling, is expressed in the lesser epithelial ridge and at gradually higher levels towards the apex. The graded expression pattern of Fst is established at the time of cochlear specification and maintained throughout embryonic and postnatal development, suggesting its possible role in the organization of tonotopy. Our data will provide a good resource for investigating the developmental mechanisms of the mammalian cochlea including the acquisition of tonotopy.
哺乳动物耳蜗管在音调上是有组织的,基底耳蜗调谐到高频声音,而顶端耳蜗调谐到低频声音。为了了解这种音调组织是如何建立的,我们搜索了在新生儿发育过程中沿音调轴差异表达的基因。从 P0 和 P8 小鼠中分离出的耳蜗组织被分成相等的三份,代表基底、中部和顶端,并使用微阵列技术确定基因表达谱。根据沿音调轴的表达水平变化以及新生儿发育过程中的变化,将基因表达谱进行分组。分类后的组进一步通过功能注释聚类分析进行分析,以确定是否与特定生物学功能或过程相关的基因在每个组中特别丰富。这些分析确定了几个候选基因,这些基因可能参与耳蜗发育和音调获取。我们在发育中的小鼠耳蜗中检查了一些候选基因的表达域。Tnc(tenacin C)和 Nov(成神经细胞瘤过表达基因)在基底膜中表达,向顶端表达增加,这可能有助于沿音调轴基底膜结构的渐变变化。此外,Fst(Follistatin)是 TGF-β/BMP 信号的拮抗剂,在较小的上皮嵴中表达,并向顶端逐渐增加。Fst 的分级表达模式在耳蜗特化时建立,并在胚胎和出生后发育过程中保持不变,表明其在音调组织中的可能作用。我们的数据将为研究哺乳动物耳蜗的发育机制,包括音调获取,提供一个很好的资源。