Hawkins R David, Bashiardes Stavros, Helms Cynthia A, Hu Lydia, Saccone Nancy Lim, Warchol Mark E, Lovett Michael
Division of Human Genetics, Department of Genetics, Washington University School of Medicine, 4566 Scott Avenue, St Louis, MO 63110, USA.
Hum Mol Genet. 2003 Jun 1;12(11):1261-72. doi: 10.1093/hmg/ddg150.
The sensory receptors for hearing and balance are the hair cells of the cochlea and vestibular organs of the inner ear. Permanent hearing and balance deficits can be triggered by genetic susceptibilities or environmental factors such as infection. Unlike mammalian hair cells that have a limited capacity for regeneration, the vestibular organ of the avian ear is constantly undergoing hair cell regeneration, whereas the avian cochlea undergoes regeneration only when hair cells are damaged. In order to gain insights into the genetic programs that govern the regenerative capacity of hair cells, we interrogated custom human cDNA microarrays with sensory epithelial cell targets from avian inner ears. The arrays contained probes from conserved regions of approximately 400 genes expressed primarily in the inner ear and approximately 1500 transcription factors (TF). Highly significant differences were observed for 20 inner-ear genes and more than 80 TFs. Genes up-regulated in the cochlea included BMP4, GATA3, GSN, FOXF1 and PRDM7. Genes up-regulated in the utricle included SMAD2, KIT, beta-AMYLOID, LOC51637, HMG20B and CRIP2. Many of the highly significant changes were validated by Q-PCR and in situ methods. Some of the observed changes implicated a number of known biochemical pathways including the c-kit pathway previously observed in melanogenesis. Twenty differentially expressed TFs map to chromosomal regions harboring uncloned human deafness loci, and represent novel candidates for hearing loss. The approach described here also illustrates the power of utilizing conserved human cDNA probes for cross-species comparisons.
听觉和平衡的感觉感受器是内耳耳蜗和前庭器官的毛细胞。永久性听力和平衡缺陷可能由遗传易感性或感染等环境因素引发。与哺乳动物毛细胞再生能力有限不同,鸟类内耳的前庭器官不断进行毛细胞再生,而鸟类耳蜗仅在毛细胞受损时才进行再生。为了深入了解控制毛细胞再生能力的基因程序,我们用鸟类内耳的感觉上皮细胞靶标检测了定制的人类cDNA微阵列。这些阵列包含来自主要在内耳表达的约400个基因的保守区域的探针和约1500个转录因子(TF)。在20个内耳基因和80多个TF中观察到高度显著的差异。耳蜗中上调的基因包括BMP4、GATA3、GSN、FOXF1和PRDM7。椭圆囊中上调的基因包括SMAD2、KIT、β-淀粉样蛋白、LOC51637、HMG20B和CRIP2。许多高度显著的变化通过定量PCR和原位方法得到验证。一些观察到的变化涉及许多已知的生化途径,包括先前在黑色素生成中观察到的c-kit途径。20个差异表达的TF定位于含有未克隆人类耳聋基因座的染色体区域,是听力损失的新候选基因。这里描述的方法也说明了利用保守的人类cDNA探针进行跨物种比较的作用。