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Fast-forward genetics identifies plant CPL phosphatases as regulators of miRNA processing factor HYL1

机译:快进遗传学鉴定植物CPL磷酸酶是miRNA加工因子HYL1的调节剂

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摘要

MicroRNAs (miRNAs) are processed from primary transcripts that contain partially self-complementary foldbacks. As in animals, the core microprocessor in plants is a Dicer protein, DICER-LIKE1 (DCL1). Processing accuracy and strand selection is greatly enhanced through the RNA binding protein HYPONASTIC LEAVES 1 (HYL1) and the zinc finger protein SERRATE (SE). We have combined a luciferase-based genetic screen with whole-genome sequencing for rapid identification of new regulators of miRNA biogenesis and action. Among the first six mutants analyzed were three alleles of C-TERMINAL DOMAIN PHOSPHATASE-LIKE 1 (CPL1)/FIERY2 (FRY2). In the miRNA processing complex, SE functions as a scaffold to mediate CPL1 interaction with HYL1, which needs to be dephosphorylated for optimal activity. In the absence of CPL1, HYL1 dephosphorylation and hence accurate processing and strand selection from miRNA duplexes are compromised. Our findings thus define a new regulatory step in plant miRNA biogenesis.
机译:MicroRNA(miRNA)由包含部分自我互补折叠的初级转录本加工而成。与动物一样,植物的核心微处理器是Dicer蛋白DICER-LIKE1(DCL1)。 RNA结合蛋白HYPONASTIC LEAVES 1(HYL1)和锌指蛋白SERRATE(SE)大大提高了加工精度和链选择。我们已将基于荧光素酶的基因筛选与全基因组测序相结合,以快速鉴定miRNA生物发生和作用的新调节剂。在分析的前六个突变体中,有C-末端域磷酸酶样1(CPL1)/ FIERY2(FRY2)的三个等位基因。在miRNA处理复合物中,SE充当支架来介导CPL1与HYL1的相互作用,而HYL1需要进行去磷酸化才能获得最佳活性。在没有CPL1的情况下,HYL1的去磷酸化以及因此从miRNA双链体进行的精确加工和链选择会受到损害。因此,我们的发现定义了植物miRNA生物发生中的新调控步骤。

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