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

机译:Sox2介导的Six3.2差异激活有助于前脑模式的形成。

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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.
机译:脊椎动物的前脑在胃化过程中被图案化为端脑,视网膜,下丘脑和双脑原基。每个这些域的规范要求转录因子(TFs)组合的协同活动。矛盾的是,其中一些因素在前脑中得到了广泛表达,这就提出了一个问题,即它们如何调解区域差异。为了解决这个问题,我们专注于homeobox TF Six3.2。通过基因组和功能方法,我们证明了在鱼中,Six3.2在Sox2的直接控制下以浓度依赖的方式调节端脑和视网膜规格。 Six3.2和Sox2在下丘脑发育中具有拮抗作用。这些活动部分地由Foxg1和Rx3执行,它们似乎受到Six3.2和Sox2的差异化和直接调节。总之,这些数据描述了Six3.2使其在前脑中的活动多样化的机制,并突显了Sox2作为前前脑发育的主要调节剂之一的新功能。他们还证明,可能在部分独立的转录网络中起作用的同一TF的分级水平沿前后轴排列了脊椎动物前脑的模式。

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