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Evidence that a consensus element found in naturally intronless mRNAs promotes mRNA export

机译:天然无内含子mRNA中发现的共有元素促进mRNA输出的证据

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摘要

We previously showed that mRNAs synthesized from three genes that naturally lack introns contain a portion of their coding sequence, known as a cytoplasmic accumulation region (CAR), which is essential for stable accumulation of the intronless mRNAs in the cytoplasm. The CAR in each mRNA is unexpectedly large, ranging in size from ∼160 to 285 nt. Here, we identified one or more copies of a 10-nt consensus sequence in each CAR. To determine whether this element (designated CAR-E) functions in cytoplasmic accumulation of intronless mRNA, we multimerized the most conserved CAR-E and inserted it upstream of β-globin cDNA, which is normally retained/degraded in the nucleus. Significantly, the tandem CAR-E, but not its antisense counterpart, rescued cytoplasmic accumulation of β-globin cDNA transcripts. Moreover, dinucleotide mutations in the CAR-E abolished this rescue. We show that the CAR-E, but not the mutant CAR-E, associates with components of the TREX mRNA export machinery, the Prp19 complex and U2AF2. Moreover, knockdown of these factors results in nuclear retention of the intronless mRNAs. Together, these data suggest that the CAR-E promotes export of intronless mRNA by sequence-dependent recruitment of the mRNA export machinery.
机译:我们以前表明,由三个自然缺乏内含子的基因合成的mRNA包含其编码序列的一部分,称为细胞质积累区(CAR),这对于无内含子mRNA在细胞质中的稳定积累至关重要。每个mRNA中的CAR都出乎意料的大,大小在〜160到285 nt之间。在这里,我们在每个CAR中确定了一个10 nt共有序列的一个或多个副本。为了确定该元素(称为CAR-E)是否在无内含子mRNA的细胞质积累中起作用,我们将最保守的CAR-E进行了多聚化,并将其插入到通常在细胞核中保留/降解的β-珠蛋白cDNA的上游。重要的是,串联CAR-E(而非其反义对应物)拯救了β-珠蛋白cDNA转录本的细胞质积累。此外,CAR-E中的二核苷酸突变消除了这种拯救。我们显示,CAR-E,但不是突变体CAR-E,与TREX mRNA输出机器,Prp19复合物和U2AF2的组件相关联。而且,这些因素的敲除导致无内含子mRNA的核保留。总之,这些数据表明CAR-E通过mRNA出口机制的序列依赖性募集促进无内含子mRNA的出口。

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