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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:胚胎发生过程中广泛需要Notch信号,经常激活两种基本的螺旋-环-螺旋转录因子Hes1和Hes5的转录。但是,在开发过程中,Hes1和Hes5在何时何地单独或共同起作用仍然没有解决。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的替代物。我们直接比较了转基因GFP表达与Hes1,以及胚胎晶状体和视网膜发育的特定标记。结果:Hes5-GFP在视网膜和晶状体前体细胞亚群中是动态的,并分化为视网膜神经节神经元,与在所有前体细胞中发现的Hes1相比。在成人视网膜中,只有Müller胶质细胞表达Hes5-GFP。最后,Hes1种系突变体中Hes5-GFP上调,这与之前Hes1抑制Hes5转录的证明一致。结论:Hes5-GFP-BAC转基因小鼠可用于鉴定Hes5表达细胞。尽管Hes5-GFP和Hes1在特定的发育环境中共同表达,但我们也注意到,晶状体或视网膜细胞只表达一种因子。Hes5-GFP的动态表达模式,再加上其在Hes1突变体中的去表达,表明该转基因包含调节小鼠晶状体和视网膜内源性Hes5的相关顺式调节元件。发展动态247:212–2212018?2017威利期刊公司。

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