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The RNA Binding Domain of Jerky Consists of Tandemly Arranged Helix-Turn-Helix/Homeodomain-Like Motifs and Binds Specific Sets of mRNAs

机译:生涩的RNA结合结构域由串联排列的螺旋-转-螺旋/同源结构域基序组成,并结合特定的mRNA集

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摘要

A deficit in the Jerky protein in mice causes recurrent seizures reminiscent of temporal lobe epilepsy. Jerky is present in mRNA particles in neurons. We show that the N-terminal 168 amino acids of Jerky are necessary and sufficient for mRNA binding. The binding domain is similar to the two tandemly arranged homeodomain-like helix-turn-helix DNA binding motifs of centromere binding protein B. The putative helix-turn-helix motifs of Jerky can also bind double-stranded DNA and represent a novel mammalian RNA/DNA binding domain. Microarray analysis identified mRNAs encoding proteins involved in ribosome assembly and cellular stress response that specifically bound to the RNA binding domain of Jerky both in vitro and in vivo. These data suggest that epileptogenesis in Jerky-deficient mice most likely involves pathways associated with ribosome biogenesis and neuronal survival and/or apoptosis.
机译:小鼠中生涩蛋白的缺乏会引起反复发作,使人联想起颞叶癫痫。生涩存在于神经元的mRNA颗粒中。我们表明,生涩的N端168个氨基酸对于mRNA结合是必要和充分的。结合结构域类似于着丝粒结合蛋白B的两个串联排列的同源结构域类似的螺旋-转-螺旋DNA结合基序。推定的Jerky螺旋-转-螺旋基序也可以结合双链DNA并代表新的哺乳动物RNA / DNA结合域。微阵列分析鉴定了编码与核糖体组装和细胞应激反应有关的蛋白质的mRNA,这些蛋白质在体外和体内均特异性结合至生涩的RNA结合域。这些数据表明,生涩缺陷型小鼠中的癫痫发生最可能涉及与核糖体生物发生,神经元存活和/或凋亡相关的途径。

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