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Identification of Gbp2 as a novel poly(A)+ RNA-binding protein involved in the cytoplasmic delivery of messenger RNAs in yeast

机译:Gbp2鉴定为一种新型的poly(A)+ RNA结合蛋白参与酵母中信使RNA的胞质传递

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摘要

Important progress in understanding messenger RNA export from the nucleus could be achieved by increasing the list of proteins that are involved in this process. Here, we present the identification of Gbp2 as a novel shuttling RNA-binding protein in Saccharomyces cerevisiae. Nuclear import of Gbp2 is dependent on the receptor Mtr10 and the serine/arginine-specific protein kinase Sky1. Deletion of the genes encoding both of these proteins or disruption of two of the arginine/serine repeats each shifts the steady-state localization of Gbp2 to the cytoplasm. Interestingly, deletion of MTR10 only also causes an increase in poly(A)+ RNA binding by Gbp2, suggesting a role of Mtr10 in the dissociation of Gbp2 from mRNA in the cytoplasm. The nuclear export of Gbp2 is always coupled to mRNA export and is dependent on continuous RNA polymerase II transcription and mRNA-export factors. Although GBP2 is not essential for normal cell growth, overexpression of this gene is toxic and causes a nuclear retention of bulk poly(A)+ RNA. Together, our findings clearly show an involvement of Gbp2 in mRNA transport. In addition, as a non-essential protein, Gbp2 also has the interesting potential to be spatially or temporally regulated.
机译:通过增加参与该过程的蛋白质清单,可以在理解信使RNA从细胞核输出方面取得重要进展。在这里,我们介绍了作为酿酒酵母中一种新型穿梭RNA结合蛋白的Gbp2的鉴定。 Gbp2的核输入取决于受体Mtr10和丝氨酸/精氨酸特异性蛋白激酶Sky1。缺失编码这两种蛋白质的基因或破坏精氨酸/丝氨酸中的两个重复序列,每个都将Gbp2的稳态定位转移到细胞质。有趣的是,MTR10的缺失也仅引起Gbp2结合poly(A) + RNA的增加,表明Mtr10在Gbp2从细胞质中的mRNA分离中的作用。 Gbp2的核输出始终与mRNA输出耦合,并且取决于连续RNA聚合酶II转录和mRNA输出因子。尽管GBP2对于正常细胞的生长不是必需的,但是该基因的过表达是有毒的,并且会导致大量poly(A) + RNA的核保留。在一起,我们的发现清楚地表明Gbp2参与mRNA的运输。另外,作为非必需蛋白,Gbp2也具有在空间或时间上受到调节的有趣潜力。

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