首页> 外文期刊>Nucleic Acids Research >Growth-regulated expression and G0-specific turnover of the mRNA that encodes URH49, a mammalian DExH/D box protein that is highly related to the mRNA export protein UAP56
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Growth-regulated expression and G0-specific turnover of the mRNA that encodes URH49, a mammalian DExH/D box protein that is highly related to the mRNA export protein UAP56

机译:编码URH49的mRNA的生长调节表达和G0特异性更新,URH49是与mRNA出口蛋白UAP56高度相关的哺乳动物DExH / D盒蛋白

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URH49 is a mammalian protein that is 90% identical to the DExH/D box protein UAP56, an RNA helicase that is important for splicing and nuclear export of mRNA. Although Saccharomyces cerevisiae and Drosophila express only a single protein corresponding to UAP56, mRNAs encoding URH49 and UAP56 are both expressed in human and mouse cells. Both proteins interact with the mRNA export factor Aly and both are able to rescue the loss of Sub2p (the yeast homolog of UAP56), indicating that both proteins have similar functions. UAP56 mRNA is more abundant than URH49 mRNA in many tissues, although in testes URH49 mRNA is much more abundant. UAP56 and URH49 mRNAs are present at similar levels in proliferating cultured cells. However, when the cells enter quiescence, the URH49 mRNA level decreases 3–6-fold while the UAP56 mRNA level remains relatively constant. The amount of URH49 mRNA increases to the level found in proliferating cells within 5 h when quiescent cells are growth-stimulated or when protein synthesis is inhibited. URH49 mRNA is relatively unstable (T = 4 h) in quiescent cells, but is stabilized immediately following growth stimulation or inhibition of protein synthesis. In contrast, there is much less change in the content or stability of UAP56 mRNA following growth stimulation. Our observations suggest that in mammalian cells, two UAP56-like RNA helicases are involved in splicing and nuclear export of mRNA. Differential expression of these helicases may lead to quantitative or qualitative changes in mRNA expression.
机译:URH49是一种哺乳动物蛋白,与DExH / D盒蛋白UAP56具有90%的同源性,后者对mRNA的剪接和核输出很重要。尽管酿酒酵母和果蝇仅表达对应于UAP56的单个蛋白质,但编码URH49和UAP56的mRNA在人和小鼠细胞中均表达。两种蛋白都与mRNA输出因子Aly相互作用,并且都能够挽救Sub2p(UAP56的酵母同源物)的丢失,表明这两种蛋白具有相似的功能。在许多组织中,UAP56 mRNA比URH49 mRNA丰富,尽管在睾丸中,URH49 mRNA更丰富。 UAP56和URH49 mRNA在增殖的培养细胞中以相似的水平存在。但是,当细胞进入静止状态时,URH49 mRNA水平降低3-6倍,而UAP56 mRNA水平保持相对恒定。当静止细胞受到生长刺激或蛋白合成受到抑制时,URH49 mRNA的量会在5小时内增加到增殖细胞中的水平。 URH49 mRNA在静止细胞中相对不稳定(T = 4 h),但在生长刺激或抑制蛋白质合成后立即稳定。相反,生长刺激后,UAP56 mRNA的含量或稳定性几乎没有变化。我们的观察结果表明,在哺乳动物细胞中,两种UAP56样RNA解旋酶参与mRNA的剪接和核输出。这些解旋酶的差异表达可能导致mRNA表达的数量或质量变化。

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