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斑马鱼和小鼠内耳毛细胞表型差异背后的分子特化

Molecular specializations underlying phenotypic differences in inner ear hair cells of zebrafish and mice.

作者信息

Giffen Kimberlee P, Liu Huizhan, Yamane Kacey L, Li Yi, Chen Lei, Kramer Kenneth L, Zallocchi Marisa, He David Z

机构信息

Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA, United States.

Department of Basic Sciences, Augusta University/University of Georgia Medical Partnership, Athens, GA, United States.

出版信息

Front Neurol. 2024 Oct 17;15:1437558. doi: 10.3389/fneur.2024.1437558. eCollection 2024.

Abstract

INTRODUCTION

Hair cells (HCs) are the sensory receptors of the auditory and vestibular systems in the inner ears of vertebrates that selectively transduce mechanical stimuli into electrical activity. Although all HCs have the hallmark stereocilia bundle for mechanotransduction, HCs in non-mammals and mammals differ in their molecular specialization in the apical, basolateral, and synaptic membranes. HCs of non-mammals, such as zebrafish (zHCs), are electrically tuned to specific frequencies and possess an active process in the stereocilia bundle to amplify sound signals. Mammalian HCs, in contrast, are not electrically tuned and achieve amplification by somatic motility of outer HCs (OHCs).

METHODS

To understand the genetic mechanisms underlying differences between adult zebrafish and mammalian HCs, we compared their RNA-seq-characterized transcriptomes, focusing on protein-coding orthologous genes related to HC specialization.

RESULTS

There was considerable shared expression of gene orthologs among the HCs, including those genes associated with mechanotransduction, ion transport/channels, and synaptic signaling. However, there were some notable differences in expression among zHCs, OHCs, and inner HCs (IHCs), which likely underlie the distinctive physiological properties of each cell type. For example, OHCs highly express Slc26a5 which encodes the motor protein prestin that contributes to OHC electromotility. However, zHCs have only weak expression of slc26a5, and subsequently showed no voltage-dependent electromotility when measured. Notably, the zHCs expressed more paralogous genes including those associated with HC-specific functions and transcriptional activity, though it is unknown whether they have functions similar to their mammalian counterparts. There was overlap in the expressed genes associated with a known hearing phenotype.

DISCUSSION

Our analyses unveil substantial differences in gene expression patterns that may explain phenotypic specialization of zebrafish and mouse HCs. This dataset also includes several protein-coding genes to further the functional characterization of HCs and study of HC evolution from non-mammals to mammals.

摘要

引言

毛细胞(HCs)是脊椎动物内耳听觉和前庭系统的感觉感受器,可将机械刺激选择性地转化为电活动。尽管所有毛细胞都具有用于机械转导的标志性静纤毛束,但非哺乳动物和哺乳动物的毛细胞在其顶端、基底外侧和突触膜的分子特化方面存在差异。非哺乳动物的毛细胞,如斑马鱼的毛细胞(zHCs),可对特定频率进行电调谐,并在静纤毛束中具有主动放大声音信号的过程。相比之下,哺乳动物的毛细胞不进行电调谐,而是通过外毛细胞(OHCs)的体细胞运动来实现放大。

方法

为了解成年斑马鱼和哺乳动物毛细胞之间差异的遗传机制,我们比较了它们经RNA测序表征的转录组,重点关注与毛细胞特化相关的蛋白质编码直系同源基因。

结果

毛细胞之间存在大量基因直系同源物的共同表达,包括那些与机械转导、离子运输/通道和突触信号相关的基因。然而,zHCs、OHCs和内毛细胞(IHCs)之间在表达上存在一些显著差异,这可能是每种细胞类型独特生理特性的基础。例如,OHCs高度表达Slc26a5,该基因编码有助于OHC电运动的运动蛋白prestin。然而,zHCs中slc26a5的表达较弱,随后在测量时未显示出电压依赖性电运动。值得注意的是,zHCs表达了更多的旁系同源基因,包括那些与毛细胞特异性功能和转录活性相关的基因,尽管它们是否具有与其哺乳动物对应物相似的功能尚不清楚。与已知听力表型相关的表达基因存在重叠。

讨论

我们的分析揭示了基因表达模式的显著差异,这可能解释了斑马鱼和小鼠毛细胞的表型特化。该数据集还包括几个蛋白质编码基因,以进一步明确毛细胞的功能特征,并研究从非哺乳动物到哺乳动物的毛细胞进化。

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