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Elongation factor 1 alpha 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-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 similar to 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 1 alpha (eEF1 alpha). 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 eEF1 alpha, and that eEF1 alpha-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与50-kDa相似的蛋白质的复合物。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,蛋白质印迹,质谱和超位移测定法,该蛋白质被鉴定为延伸因子1 alpha(eEF1 alpha)。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。预计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eEF1 alpha结合,并且eEF1 alpha-细胞骨架相互作用在核周mRNA定位中起作用。

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