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Separate and coincident expression of Hes1 Hes1 and Hes5 Hes5 in the developing mouse eye

机译:HES1 HES1和HES5 HES5的分开和巧合的表达在显影的小鼠眼中

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Background : Notch signaling is broadly required during embryogenesis, frequently activating the transcription of two basic helix–loop–helix transcription factors, Hes1 and Hes5 . But, it remains unresolved when and where Hes1 and Hes5 act alone or together during development. Here, we analyzed a Hes5‐green fluorescent protein (GFP) bacterial artificial chromosome (BAC) transgenic mouse, as a proxy for endogenous Hes5. We directly compared transgenic GFP expression with Hes1, and particular markers of embryonic lens and retina development. Results : Hes5‐GFP is dynamic within subsets of retinal and lens progenitor cells, and differentiating retinal ganglion neurons, in contrast to Hes1 found in all progenitor cells. In the adult retina, only Müller glia express Hes5‐GFP. Finally, Hes5‐GFP is up‐regulated in Hes1 germline mutants, consistent with previous demonstration that Hes1 suppresses Hes5 transcription. Conclusions : Hes5‐GFP BAC transgenic mice are useful for identifying Hes5 ‐expressing cells. Although Hes5‐GFP and Hes1 are coexpressed in particular developmental contexts, we also noted cohorts of lens or retinal cells expressing just one factor. The dynamic Hes5‐GFP expression pattern, coupled with its derepressed expression in Hes1 mutants, suggests that this transgene contains the relevant cis ‐regulatory elements that regulate endogenous Hes5 in the mouse lens and retina. Developmental Dynamics 247:212–221, 2018 . ? 2017 Wiley Periodicals, Inc.
机译:背景:胚胎发生期间广泛需要Notch信号,经常激活两个基本螺旋环螺旋转录因子的转录,HES1和HES5。但是,它仍然未解决,当时HES1和HES5在开发期间独自或在一起。在这里,我们分析了HES5绿色荧光蛋白(GFP)细菌人工染色体(BAC)转基因小鼠,作为内源性HES5的代理。我们直接与HES1进行转基因GFP表达,以及胚胎透镜的特定标志物和视网膜发育。结果:HES5-GFP在视网膜和晶状体祖细胞的子集内是动态的,并且与所有祖细胞中发现的HES1相比,分化视网膜神经节神经元。在成人视网膜中,只有MüllerGlia表达HES5-GFP。最后,HES5-GFP在HES1种系突变体中调高,与之前的示威性一致,HES1抑制了HES5转录。结论:HES5-GFP BAC转基因小鼠可用于鉴定HES5 -Expressing细胞。虽然HES5-GFP和HES1在特定的发展环境中被共表达,但我们还注意到透镜或视网膜细胞的群体仅表达一个因素。动态HES5-GFP表达模式与其在HES1突变体中的重症表达相结合,表明该转基因含有相关的CIS -Regulatory元素,其调节在小鼠镜片和视网膜中的内源性HES5。发展动力学247:212-221,2018。还2017年Wiley期刊,Inc。

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