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Reciprocal regulation of glycine-rich RNA-binding proteins via an interlocked feedback loop coupling alternative splicing to nonsense-mediated decay in Arabidopsis

机译:通过互锁的反馈环相互耦合调节富含甘氨酸的RNA结合蛋白,所述剪接环与拟南芥中无义介导的衰变的选择性剪接偶联

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The Arabidopsis RNA-binding protein AtGRP8 undergoes negative autoregulation at the post-transcriptional level. An elevated AtGRP8 protein level promotes the use of a cryptic 5′ splice site to generate an alternatively spliced transcript, as_AtGRP8, retaining the 5′ half of the intron with a premature termination codon. In mutants defective in nonsense-mediated decay (NMD) abundance of as_AtGRP8 but not its pre-mRNA is elevated, indicating that as_AtGRP8 is a direct NMD target, thus limiting the production of functional AtGRP8 protein. In addition to its own pre-mRNA, AtGRP8 negatively regulates the AtGRP7 transcript through promoting the formation of the equivalent alternatively spliced as_AtGRP7 transcript, leading to a decrease in AtGRP7 abundance. Recombinant AtGRP8 binds to its own and the AtGRP7 pre-mRNA, suggesting that this interaction is relevant for the splicing decision in vivo. AtGRP7 itself is part of a negative autoregulatory circuit that influences circadian oscillations of its own and the AtGRP8 transcript through alternative splicing linked to NMD. Thus, we identify an interlocked feedback loop through which two RNA-binding proteins autoregulate and reciprocally crossregulate by coupling unproductive splicing to NMD. A high degree of evolutionary sequence conservation in the introns retained in as_AtGRP8 or as_AtGRP7 points to an important function of these sequences.
机译:拟南芥RNA结合蛋白AtGRP8在转录后水平经历负的自我调节。升高的AtGRP8蛋白水平促进了隐性5'剪接位点的使用,以产生选择性剪接的转录本as_AtGRP8,保留了内含子5'的一半带有过早的终止密码子。在无义介导的衰变(NMD)有缺陷的突变体中,as_AtGRP8的丰度升高,但其pre-mRNA却没有升高,表明as_AtGRP8是直接的NMD靶标​​,从而限制了功能性AtGRP8蛋白的产生。除了自身的pre-mRNA以外,AtGRP8还通过促进等价交替剪接的as_AtGRP7转录物的形成来负调控AtGRP7转录物,从而导致AtGRP7丰度降低。重组AtGRP8与其自身和AtGRP7 pre-mRNA结合,表明这种相互作用与体内剪接决定有关。 AtGRP7本身是负自动调节电路的一部分,该电路通过与NMD相连的可变剪接影响其自身的昼夜节律振荡和AtGRP8转录物。因此,我们确定了一个互锁的反馈回路,通过该回路,两个RNA结合蛋白通过将非生产性剪接偶联至NMD而自动调节和相互交叉调节。保留在as_AtGRP8或as_AtGRP7中的内含子中高度的进化序列保守性指示这些序列的重要功能。

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