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Pou3f1精心编排一个控制对侧视网膜神经节细胞投射的基因调控网络。

Pou3f1 orchestrates a gene regulatory network controlling contralateral retinogeniculate projections.

作者信息

Fries Michel, Brown Thomas W, Jolicoeur Christine, Boulan Benoit, Boudreau-Pinsonneault Camille, Javed Awais, Abram Pénélope, Cayouette Michel

机构信息

Cellular Neurobiology Research Unit, Institut de Recherches Cliniques de Montréal, Montreal, QC H2W 1R7, Canada; Molecular Biology Program, Université de Montréal, Montreal, QC H3C 3J7, Canada.

Cellular Neurobiology Research Unit, Institut de Recherches Cliniques de Montréal, Montreal, QC H2W 1R7, Canada; Integrated Program in Neuroscience, McGill University, Montreal, QC H3A 1A1, Canada.

出版信息

Cell Rep. 2023 Aug 29;42(8):112985. doi: 10.1016/j.celrep.2023.112985. Epub 2023 Aug 16.

Abstract

The balance of contralateral and ipsilateral retinogeniculate projections is critical for binocular vision, but the transcriptional programs regulating this process remain ill defined. Here we show that the Pou class homeobox protein POU3F1 is expressed in nascent mouse contralateral retinal ganglion cells (cRGCs) but not ipsilateral RGCs (iRGCs). Upon Pou3f1 inactivation, the proportion of cRGCs is reduced in favor of iRGCs, leading to abnormal projection ratios at the optic chiasm. Conversely, misexpression of Pou3f1 in progenitors increases the production of cRGCs. Using CUT&RUN and RNA sequencing in gain- and loss-of-function assays, we demonstrate that POU3F1 regulates expression of several key members of the cRGC gene regulatory network. Finally, we report that POU3F1 is sufficient to induce RGC-like cell production, even in late-stage retinal progenitors of Atoh7 knockout mice. This work uncovers POU3F1 as a regulator of the cRGC transcriptional program, opening possibilities for optic nerve regenerative therapies.

摘要

对侧和同侧视网膜神经节细胞投射的平衡对于双眼视觉至关重要,但调节这一过程的转录程序仍不清楚。在这里,我们表明,Pou类同源框蛋白POU3F1在新生小鼠对侧视网膜神经节细胞(cRGCs)中表达,而在同侧视网膜神经节细胞(iRGCs)中不表达。在Pou3f1失活后,cRGCs的比例降低,有利于iRGCs,导致视交叉处的投射比例异常。相反,Pou3f1在祖细胞中的错误表达增加了cRGCs的产生。在功能获得和功能丧失试验中使用CUT&RUN和RNA测序,我们证明POU3F1调节cRGC基因调控网络的几个关键成员的表达。最后,我们报告POU3F1足以诱导RGC样细胞的产生,即使在Atoh7基因敲除小鼠的晚期视网膜祖细胞中也是如此。这项工作揭示了POU3F1作为cRGC转录程序的调节因子,为视神经再生疗法开辟了可能性。

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