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通过Eya2基因敲入报告基因揭示的小鼠胚胎发育过程中的Eya2表达以及纯合小鼠表现出轻度听力损失。

Eya2 expression during mouse embryonic development revealed by Eya2 knockin reporter and homozygous mice show mild hearing loss.

作者信息

Zhang Ting, Xu Jinshu, Xu Pin-Xian

机构信息

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

Dev Dyn. 2021 Oct;250(10):1450-1462. doi: 10.1002/dvdy.326. Epub 2021 Mar 19.

Abstract

BACKGROUND

Eya2 expression during mouse development has been studied by in situ hybridization and it has been shown to be involved skeletal muscle development and limb formation. Here, we generated Eya2 knockout (Eya2 ) and a lacZ knockin reporter (Eya2 ) mice and performed a detailed expression analysis for Eya2 at different developmental stages to trace Eya2 -positive cells in Eya2-null mice. We describe that Eya2 is not only expressed in cranial sensory and dorsal root ganglia, retina and olfactory epithelium, and somites as previously reported, but also Eya2 is specifically detected in other organs during mouse development.

RESULTS

We found that Eya2 is expressed in ocular and trochlear motor neurons. In the inner ear, Eya2 is specifically expressed in differentiating hair cells in both vestibular and cochlear sensory epithelia of the inner ear and Eya2 or Eya2 mice displayed mild hearing loss. Furthermore, we detected Eya2 expression during both salivary gland and thymus development and Eya2-null mice had a smaller thymus.

CONCLUSIONS

As Eya2 is coexpressed with other members of the Eya family genes, these results together highlight that Eya2 as a potential regulator may act synergistically with other Eya genes to regulate the differentiation of the inner ear sensory hair cells and the formation of the salivary gland and thymus.

摘要

背景

通过原位杂交研究了小鼠发育过程中Eya2的表达,结果表明其参与骨骼肌发育和肢体形成。在此,我们构建了Eya2基因敲除(Eya2-/-)和lacZ基因敲入报告基因(Eya2lacZ/+)小鼠,并对不同发育阶段的Eya2进行了详细的表达分析,以追踪Eya2基因敲除小鼠中Eya2阳性细胞。我们发现,Eya2不仅如先前报道的那样在颅感觉神经节、背根神经节、视网膜和嗅上皮以及体节中表达,而且在小鼠发育过程中还在其他器官中特异性表达。

结果

我们发现Eya2在动眼神经和滑车神经运动神经元中表达。在内耳中,Eya2在内耳前庭和耳蜗感觉上皮的分化毛细胞中特异性表达,Eya2-/-或Eya2lacZ/+小鼠表现出轻度听力损失。此外,我们在唾液腺和胸腺发育过程中检测到Eya2表达,Eya2基因敲除小鼠的胸腺较小。

结论

由于Eya2与Eya家族基因的其他成员共表达,这些结果共同表明,Eya2作为一种潜在的调节因子,可能与其他Eya基因协同作用,调节内耳感觉毛细胞的分化以及唾液腺和胸腺的形成。

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