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伊卡洛斯家族蛋白在发育中的小鼠视网膜中对时间模式进行冗余调节。

Ikaros family proteins redundantly regulate temporal patterning in the developing mouse retina.

作者信息

Javed Awais, Santos-França Pedro L, Mattar Pierre, Cui Allie, Kassem Fatima, Cayouette Michel

机构信息

Cellular Neurobiology Research Unit, Institut de recherches cliniques de Montréal (IRCM), Montreal H2W 1R7, Canada.

Molecular Biology Program, Université de Montréal, Montreal H3T 1J4, Canada.

出版信息

Development. 2023 Jan 15;150(2). doi: 10.1242/dev.200436. Epub 2023 Jan 16.

Abstract

Temporal identity factors regulate competence of neural progenitors to generate specific cell types in a time-dependent manner, but how they operate remains poorly defined. In the developing mouse retina, the Ikaros zinc-finger transcription factor Ikzf1 regulates production of early-born cell types, except cone photoreceptors. In this study we show that, during early stages of retinal development, another Ikaros family protein, Ikzf4, functions redundantly with Ikzf1 to regulate cone photoreceptor production. Using CUT&RUN and functional assays, we show that Ikzf4 binds and represses genes involved in late-born rod photoreceptor specification, hence favoring cone production. At late stages, when Ikzf1 is no longer expressed in progenitors, we show that Ikzf4 re-localizes to target genes involved in gliogenesis and is required for Müller glia production. We report that Ikzf4 regulates Notch signaling genes and is sufficient to activate the Hes1 promoter through two Ikzf GGAA-binding motifs, suggesting a mechanism by which Ikzf4 may influence gliogenesis. These results uncover a combinatorial role for Ikaros family members during nervous system development and provide mechanistic insights on how they temporally regulate cell fate output.

摘要

时间身份因子以时间依赖的方式调节神经祖细胞产生特定细胞类型的能力,但其作用机制仍不清楚。在发育中的小鼠视网膜中,Ikaros锌指转录因子Ikzf1调节除视锥光感受器外的早期生成细胞类型的产生。在本研究中,我们发现,在视网膜发育的早期阶段,另一种Ikaros家族蛋白Ikzf4与Ikzf1发挥冗余功能,以调节视锥光感受器的产生。通过CUT&RUN和功能分析,我们表明Ikzf4结合并抑制参与晚期生成的视杆光感受器特化的基因,从而有利于视锥细胞的产生。在晚期,当Ikzf1在祖细胞中不再表达时,我们发现Ikzf4重新定位到参与神经胶质生成的靶基因,并且是米勒胶质细胞产生所必需的。我们报告说,Ikzf4调节Notch信号基因,并且足以通过两个Ikzf GGAA结合基序激活Hes1启动子,这表明Ikzf4可能影响神经胶质生成的机制。这些结果揭示了Ikaros家族成员在神经系统发育过程中的组合作用,并为它们如何在时间上调节细胞命运输出提供了机制上的见解。

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