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Rbfox1以多种转录变体的形式在小鼠脑中表达,并且在其可变启动子中包含功能性E盒。

Rbfox1 Is Expressed in the Mouse Brain in the Form of Multiple Transcript Variants and Contains Functional E Boxes in Its Alternative Promoters.

作者信息

Casanovas Sonia, Schlichtholz Laura, Mühlbauer Sophia, Dewi Sri, Schüle Martin, Strand Dennis, Strand Susanne, Zografidou Lea, Winter Jennifer

机构信息

Institute of Human Genetics, University Medical Center Mainz, Mainz, Germany.

Focus Program of Translational Neurosciences, University Medical Center Mainz, Mainz, Germany.

出版信息

Front Mol Neurosci. 2020 May 5;13:66. doi: 10.3389/fnmol.2020.00066. eCollection 2020.

Abstract

The RNA-binding protein RBFOX1 is an important regulator of neuron development and neuronal excitability. is a dosage-sensitive gene and in both mice and humans, decreased expression of has been linked to neurodevelopmental disorders. Alternative promoters drive expression of transcript isoforms that encode an identical protein. The tissue- and developmental stage-specific expression of these isoforms, as well as the underlying regulatory mechanisms, are, however, unclear. Here, we set out to capture all of the Rbfox1 transcript isoforms and identify transcriptional mechanisms that regulate brain-specific expression. Isoform sequencing identified multiple alternative transcript variants in the mouse cerebral cortex, including transcripts with novel first exons, alternatively spliced exons and 3'-truncations. Quantitative RT-PCR determined the expression of the alternative first exons in the developing cerebral cortex and different subregions of the juvenile brain. Alternative first exons were found to be highly stage- and subregion specific in their expression patterns suggesting that they fulfill specific functions during cortex development and in different brain regions. Using reporter assays we found that the promoter regions of the two first exons E1B and E1C/E1C.1 contain several functional E-boxes. Together, we provide an extensive picture of isoform expression. We further identified important regulatory mechanisms that drive neuron-specific expression. Thus, our study forms the basis for further research into the mechanisms that ensure physiological expression in the brain. It also helps to understand why, in patients with neurodevelopmental disorders deletion of individual transcript isoforms could affect brain function.

摘要

RNA结合蛋白RBFOX1是神经元发育和神经元兴奋性的重要调节因子。它是一个剂量敏感基因,在小鼠和人类中,其表达降低都与神经发育障碍有关。可变启动子驱动编码相同蛋白质的转录本异构体的表达。然而,这些异构体在组织和发育阶段的特异性表达以及潜在的调控机制尚不清楚。在这里,我们着手捕获所有的Rbfox1转录本异构体,并确定调节大脑特异性表达的转录机制。异构体测序在小鼠大脑皮层中鉴定出多个可变的转录本变体,包括具有新的第一个外显子、可变剪接外显子和3'端截短的转录本。定量逆转录-聚合酶链反应测定了发育中的大脑皮层和幼龄大脑不同亚区域中可变第一个外显子的表达。发现可变第一个外显子在其表达模式上具有高度的阶段和亚区域特异性,这表明它们在皮层发育和不同脑区中发挥特定功能。通过报告基因分析,我们发现两个第一个外显子E1B和E1C/E1C.1的启动子区域包含几个功能性E盒。我们共同提供了一幅关于异构体表达的详尽图景。我们进一步确定了驱动神经元特异性表达的重要调控机制。因此,我们的研究为进一步研究确保大脑中生理表达的机制奠定了基础。它也有助于理解为什么在神经发育障碍患者中,单个转录本异构体的缺失会影响脑功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9853/7214753/2cf9347dba9f/fnmol-13-00066-g0001.jpg

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