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Sox2 介导的 Six3.2 差异激活有助于前脑模式形成。

Sox2-mediated differential activation of Six3.2 contributes to forebrain patterning.

机构信息

Centro de Biología Molecular Severo Ochoa, CSIC-UAM, c/Nicolas Cabrera 1, Madrid 28049, Spain.

出版信息

Development. 2012 Jan;139(1):151-64. doi: 10.1242/dev.067660. Epub 2011 Nov 17.

Abstract

The vertebrate forebrain is patterned during gastrulation into telencephalic, retinal, hypothalamic and diencephalic primordia. Specification of each of these domains requires the concerted activity of combinations of transcription factors (TFs). Paradoxically, some of these factors are widely expressed in the forebrain, which raises the question of how they can mediate regional differences. To address this issue, we focused on the homeobox TF Six3.2. With genomic and functional approaches we demonstrate that, in medaka fish, Six3.2 regulates, in a concentration-dependent manner, telencephalic and retinal specification under the direct control of Sox2. Six3.2 and Sox2 have antagonistic functions in hypothalamic development. These activities are, in part, executed by Foxg1 and Rx3, which seem to be differentially and directly regulated by Six3.2 and Sox2. Together, these data delineate the mechanisms by which Six3.2 diversifies its activity in the forebrain and highlight a novel function for Sox2 as one of the main regulators of anterior forebrain development. They also demonstrate that graded levels of the same TF, probably operating in partially independent transcriptional networks, pattern the vertebrate forebrain along the anterior-posterior axis.

摘要

脊椎动物前脑在原肠胚形成过程中被模式化为端脑、视网膜、下丘脑和间脑原基。这些区域的特化需要转录因子 (TFs) 的组合协同作用。矛盾的是,这些因子中的一些在大脑中广泛表达,这就提出了它们如何介导区域差异的问题。为了解决这个问题,我们专注于同源盒 TF Six3.2。通过基因组和功能方法,我们证明在斑马鱼中,Six3.2 以浓度依赖的方式调节 Sox2 直接控制下的端脑和视网膜特化。Six3.2 和 Sox2 在下丘脑发育中具有拮抗作用。这些活性部分由 Foxg1 和 Rx3 执行,它们似乎受 Six3.2 和 Sox2 的差异和直接调节。这些数据共同描绘了 Six3.2 在前脑多样化其活性的机制,并强调了 Sox2 作为前脑发育主要调节剂之一的新功能。它们还表明,相同 TF 的分级水平可能在部分独立的转录网络中运作,沿前后轴对脊椎动物前脑进行模式化。

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