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Elongation factor 1α binds to the region of the metallothionein-1 mRNA implicated in perinuclear localization—importance of an internal stem–loop

机译:延伸因子1α结合到与周围核定位有关的金属硫蛋白-1 mRNA的区域中-内部茎环的重要性

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摘要

In eukaryotic cells, mRNA localization can provide local protein synthesis. Metallothionein-1 (MT-1) mRNA is associated with the perinuclear cytoskeleton, and this is essential for subsequent nuclear import of the protein. The present study defines the cis-acting localization signal and a trans-acting binding protein. Gel retardation and UV cross-linking assays using MT-1 3′UTR transcripts and CHO cell extracts revealed formation of a complex containing a ∼50-kDa protein. Only localization-positive mutant transcripts competed for binding of this protein. Using an RNA affinity technique, Western blotting, mass spectrometry, and a supershift assay, the protein was identified as Elongation factor 1α (eEF1α). Mutation and deletion analysis showed that two regions, nucleotides 21–36 and 66–76, were required for both binding and localization. RNA-folding prediction combined with chemical and enzymatic probing experiments suggest that these regions are in juxtaposition within a stem/internal loop structure. Mutations that are predicted to alter this structure abrogate protein binding. Our hypothesis is that the cis-acting signal in MT-1 3′UTR is formed by this stem/internal loop, that it binds eEF1α, and that eEF1α–cytoskeleton interactions play a role in perinuclear mRNA localization.
机译:在真核细胞中,mRNA定位可以提供局部蛋白质合成。金属硫蛋白-1(MT-1)mRNA与核周细胞骨架相关,这对于随后的蛋白质核进口至关重要。本研究定义了顺式作用定位信号和反式作用结合蛋白。使用MT-1 3'UTR转录本和CHO细胞提取物进行的凝胶阻滞和UV交联测定表明形成了含有约50kDa蛋白的复合物。仅定位阳性突变体转录物竞争该蛋白的结合。使用RNA亲和技术,Western印迹,质谱和超位移测定,该蛋白质被鉴定为延伸因子1α(eEF1α)。突变和缺失分析表明,结合和定位都需要两个区域,核苷酸21–36和66–76。 RNA折叠预测结合化学和酶促探测实验表明,这些区域在茎/内部环结构内并列。预测会改变这种结构的突变会消除蛋白质结合。我们的假设是MT-1 3'UTR中的顺式作用信号是由该茎/内部环形成的,它与eEF1α结合,并且eEF1α-细胞骨架的相互作用在核周mRNA定位中起作用。

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