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Cytoplasmic Poly(A) Binding Protein C4 Serves a Critical Role in Erythroid Differentiation

机译:细胞质Poly(A)结合蛋白C4在类红细胞分化中起关键作用

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摘要

The expression of an mRNA is strongly impacted by its 3′ poly(A) tail and associated poly(A)-binding proteins (PABPs). Vertebrates encode six PABP isoforms that vary in abundance, distribution, developmental control, and subcellular localization. Here we demonstrate that the minor PABP isoform PABPC4 is expressed in erythroid cells and impacts the steady-state expression of a subset of erythroid mRNAs. Motif analyses reveal a high-value AU-rich motif in the 3′ untranslated regions (UTRs) of PABPC4-impacted mRNAs. This motif enhances the association of PABPC4 with mRNAs containing critically shortened poly(A) tails. This association may serve to protect a subset of mRNAs from accelerated decay. Finally, we demonstrate that selective depletion of PABPC4 in an erythroblast cell line inhibits terminal erythroid maturation with corresponding alterations in the erythroid gene expression. These observations lead us to conclude that PABPC4 plays an essential role in posttranscriptional control of a major developmental pathway.
机译:mRNA的表达受到其3'poly(A)尾巴和相关的poly(A)结合蛋白(PABP)的强烈影响。脊椎动物编码六种PABP亚型,它们的丰度,分布,发育控制和亚细胞定位均不同。在这里,我们证明未成年人PABP亚型PABPC4在类红细胞中表达,并影响类红细胞mRNA的稳态表达。母题分析显示,PABPC4受影响的mRNA的3'非翻译区(UTR)具有高价值的富AU基序。该基序增强了PABPC4与含有严重缩短的poly(A)尾巴的mRNA的关联。这种关联可以用于保护mRNA的子集免于加速衰减。最后,我们证明在成红细胞细胞系中PABPC4的选择性消耗会抑制末端红系成熟,并在红系基因表达中产生相应的改变。这些观察结果使我们得出结论,PABPC4在主要发育途径的转录后控制中起着至关重要的作用。

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