Zhang Ting, Xu Pin-Xian
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Department of Cell Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Front Cell Dev Biol. 2023 Apr 25;11:1126968. doi: 10.3389/fcell.2023.1126968. eCollection 2023.
Members of the Eya family, which are a class of transcription factors with phosphatase activity, are widely expressed in cranial sensory organs during development. However, it is unclear whether these genes are expressed in the taste system during development and whether they play any role in specifying taste cell fate. In this study, we report that is not expressed during embryonic tongue development but that -expressing progenitors in somites or pharyngeal endoderm give rise to tongue musculature or taste organs, respectively. In the -deficient tongues, these progenitors do not proliferate properly, resulting in a smaller tongue at birth, impaired growth of taste papillae, and disrupted expression of in the papillary epithelium. On the other hand, is specifically expressed in endoderm-derived circumvallate and foliate papillae located on the posterior tongue during development. In adult tongues, is predominantly expressed in IPR3-positive taste cells in the taste buds of the circumvallate and foliate papillae, while is persistently expressed in these papillae at higher levels in some epithelial progenitors and at lower levels in some taste cells. We found that conditional knockout of in the third week or 2 knockout reduced Pou2f3, Six1 and IPR3 taste cells. Our data define for the first time the expression patterns of and during the development and maintenance of the mouse taste system and suggest that and may act together to promote lineage commitment of taste cell subtypes.
Eya家族成员属于一类具有磷酸酶活性的转录因子,在发育过程中广泛表达于颅感觉器官。然而,目前尚不清楚这些基因在味觉系统发育过程中是否表达,以及它们在味觉细胞命运决定中是否发挥任何作用。在本研究中,我们报告称,在胚胎期舌发育过程中不表达,但体节或咽内胚层中表达的祖细胞分别产生舌肌肉组织或味觉器官。在缺乏该基因的舌中,这些祖细胞不能正常增殖,导致出生时舌较小,味蕾生长受损,以及乳头上皮中该基因的表达紊乱。另一方面,在发育过程中,该基因在舌后部由内胚层衍生的轮廓乳头和叶状乳头中特异性表达。在成年舌中,该基因主要在轮廓乳头和叶状乳头味蕾中IPR3阳性的味觉细胞中表达,而在这些乳头中,该基因在一些上皮祖细胞中持续高水平表达,在一些味觉细胞中低水平表达。我们发现,在第三周进行条件性敲除该基因或敲除两个拷贝会减少Pou2f3、Six1和IPR3味觉细胞。我们的数据首次定义了该基因和另一基因在小鼠味觉系统发育和维持过程中的表达模式,并表明这两个基因可能共同作用以促进味觉细胞亚型的谱系定向。