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生成 FLAG 标记的 Arx 基因敲入小鼠模型。

Generation of FLAG-tagged Arx knock-in mouse model.

机构信息

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Genesis. 2022 Jul;60(6-7):e23479. doi: 10.1002/dvg.23479. Epub 2022 Jun 3.

DOI:10.1002/dvg.23479
PMID:35656878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9333336/
Abstract

The Aristaless-related homeobox (ARX) is a paired-like homeodomain transcription factor playing important roles in brain development. Patients with mutations in ARX have a spectrum of neurodevelopmental disorders such as epilepsy, intellectual disability, and autism spectrum disorder, with or without structural abnormalities of the brain such as lissencephaly (smooth brain), microcephaly (small brain), and/or agenesis of the corpus callosum. Mouse models have provided important clues on the pathophysiologic roles of ARX in these disorders. However, successfully isolating specific in vivo complexes of ARX, with DNA and proteins, has remained as a challenge. To facilitate in vivo detection of ARX complexes, we generated a mouse line containing one epitope of FLAG-tag (1 × FLAG) targeted at the translational start site of the endogenous Arx gene using CRSPR/Cas9 strategy. Homozygous Flag-Arx mice are viable and fertile without gross abnormality, suggesting that the FLAG-tag does not perturb the normal function of ARX. Using a FLAG antibody, we successfully detected ARX with immunofluorescent staining and pulled down ARX in embryonic brain tissues. This Flag-Arx mouse line will be a useful tool to isolate ARX complexes from mouse tissues for many applications.

摘要

Aristoless 相关同源盒(ARX)是一种配对样同源结构域转录因子,在大脑发育中发挥重要作用。ARX 基因突变的患者表现出一系列神经发育障碍,如癫痫、智力障碍和自闭症谱系障碍,伴有或不伴有大脑结构异常,如无脑回畸形(无脑)、小头畸形(小脑袋)和/或胼胝体发育不全。小鼠模型为 ARX 在这些疾病中的病理生理作用提供了重要线索。然而,成功分离 ARX 与 DNA 和蛋白质的特定体内复合物仍然是一个挑战。为了便于体内检测 ARX 复合物,我们使用 CRISPR/Cas9 策略生成了一种携带一个 FLAG 标签(1×FLAG)的小鼠品系,该标签靶向内源性 Arx 基因的翻译起始位点。FLAG-Arx 纯合子小鼠具有活力和繁殖力,没有明显的异常,表明 FLAG 标签不会干扰 ARX 的正常功能。使用 FLAG 抗体,我们成功地通过免疫荧光染色检测到 ARX,并在胚胎脑组织中下拉 ARX。这种 Flag-Arx 小鼠品系将成为从小鼠组织中分离 ARX 复合物用于许多应用的有用工具。

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本文引用的文献

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PIK3R2/Pik3r2 Activating Mutations Result in Brain Overgrowth and EEG Changes.PIK3R2/Pik3r2 激活突变导致脑过度生长和脑电图改变。
Ann Neurol. 2020 Dec;88(6):1077-1094. doi: 10.1002/ana.25890. Epub 2020 Sep 28.
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Arx Expression Suppresses Ventralization of the Developing Dorsal Forebrain.Arx 表达抑制发育中背侧前脑的腹侧化。
Sci Rep. 2019 Jan 18;9(1):226. doi: 10.1038/s41598-018-36194-6.
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Molecular Pathways Underlying Projection Neuron Production and Migration during Cerebral Cortical Development.大脑皮质发育过程中投射神经元产生和迁移的分子通路
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Generating neuronal diversity in the mammalian cerebral cortex.在哺乳动物大脑皮层中产生神经元多样性。
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Immunohistochemical detection of FLAG-tagged endogenous proteins in knock-in mice.在敲入小鼠中对FLAG标签内源性蛋白进行免疫组织化学检测。
J Histochem Cytochem. 2015 Apr;63(4):244-55. doi: 10.1369/0022155414568101. Epub 2015 Jan 9.
6
Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations.发育中的背侧端脑Arx的条件性缺失导致类似于轻度人类ARX突变的行为表型。
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7
ARX regulates cortical intermediate progenitor cell expansion and upper layer neuron formation through repression of Cdkn1c.ARX通过抑制Cdkn1c来调节皮质中间祖细胞的扩增和上层神经元的形成。
Cereb Cortex. 2015 Feb;25(2):322-35. doi: 10.1093/cercor/bht222. Epub 2013 Aug 22.
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Neurons on the move: migration and lamination of cortical interneurons.移动中的神经元:皮质中间神经元的迁移与分层
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9
Interneuron, interrupted: molecular pathogenesis of ARX mutations and X-linked infantile spasms.中间神经元,中断:ARX 突变和 X 连锁婴儿痉挛的分子发病机制。
Curr Opin Neurobiol. 2012 Oct;22(5):859-65. doi: 10.1016/j.conb.2012.04.006. Epub 2012 May 5.
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Identification of Arx targets unveils new candidates for controlling cortical interneuron migration and differentiation.Arx靶点的鉴定揭示了控制皮质中间神经元迁移和分化的新候选物。
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