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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The BEN domain is a novel sequence-specific DNA-binding domain conserved in neural transcriptional repressors
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The BEN domain is a novel sequence-specific DNA-binding domain conserved in neural transcriptional repressors

机译:BEN结构域是一种新型的序列特异性DNA结合结构域,在神经转录阻遏物中是保守的

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摘要

We recently repotted that Drosophila Insensitive (Insv) promotes sensory organ development and has activity as a nuclear corepressor for the Notch transcription factor Suppressor of Hairless [Su(H)]. Insv lacks domains of known biochemical function but contains a single BEN domain (i.e., a "BEN-solo" protein). Our chromatin immuno-precipitation (ChIP) sequencing (ChlP-seq) analysis confirmed binding of Insensitive to Su(H) target genes in the Enhancer of split gene complex [E(spl)-C; however, de novo motif analysis revealed a novel site strongly enriched in Insv peaks (TCYAATHRGAA). We validate binding of endogenous Insv to genomic regions bearing such sites, whose associated genes are enriched for neural functions and are functionally repressed by Insv. Unexpectedly, we found that the Insv BEN domain binds specifically to this sequence motif and that Insv directly regulates transcription via this motif. We determined the crystal structure of the BEN-DNA target complex, revealing homodimeric binding of the BEN domain and extensive nucleotide contacts via a. helices and a C-terminal loop. Point mutations in key DNA-contacting residues severely impair DNA binding in vitro and capacity for transcriptional regulation in vivo. We further demonstrate DNA-binding and repression activities by the mammalian neural BEN-solo protein BEND5. Altogether, we define novel DNA-binding activity in a conserved family of transcriptional repressors, opening a molecular window on this extensive gene family.
机译:我们最近报道果蝇不敏感(Insv)促进感觉器官发育,并具有作为无毛的Notch转录因子抑制子[Su(H)]的核共抑制子的活性。 Insv缺乏已知生化功能的结构域,但包含单个BEN结构域(即“ BEN-solo”蛋白)。我们的染色质免疫沉淀(ChIP)测序(ChlP-seq)分析证实了对分裂基因复合体[E(spl)-C1的增强子中的Su(H)目标基因不敏感。然而,从头基序分析揭示了一个新位点,该位点强烈富集了Insv峰(TCYAATHRGAA)。我们验证内源Insv与带有此类位点的基因组区域的结合,其相关基因丰富了神经功能并在功能上受到了Insv的抑制。出乎意料的是,我们发现Insv BEN域与该序列基序特异性结合,并且Insv通过该基序直接调节转录。我们确定了BEN-DNA靶复合物的晶体结构,揭示了BEN域的同源二聚体结合和通过a的广泛核苷酸接触。螺旋和一个C末端环。关键的DNA接触残基中的点突变严重损害了体外的DNA结合和体内转录调控的能力。我们进一步证明了哺乳动物神经BEN-solo蛋白BEND5的DNA结合和抑制活性。总之,我们在保守的转录阻遏物家族中定义了新的DNA结合活性,从而在这个广泛的基因家族上打开了一个分子窗口。

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