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Senescent Cells Differentially Translate Senescence-Related mRNAs Via Ribosome Heterogeneity

机译:衰老细胞通过核糖体的异质性差异地翻译衰老相关的MRNA

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The ribosome has a lateral stalk which consists of rpLP0, rpLP1, and rpLP2. One of these proteins, rpLP2, is decreased in translating ribosome when cellular senescence is induced. Y-box binding protein-1 (YB-1) is also reduced in polysomal fraction of senescent cells. We discovered that rpLP2 depletion in the ribosome can cause the detachment of YB-1 in polysomes and that it is linked to cellular senescence. Our results also revealed that a decrement of CK2 alpha or GRK2 in senescent cells induced an increment of unphosphorylated rpLP2, resulting in release of YB-i from polysomes. This heterogeneous senescent ribosome has different translational efficiencies for some senescence-related genes. We also showed that the decrease of rpLP1/rpLP2 and YB-1 in senescent ribosomes was not specific to cell type or stress type and the same phenomenon was also observed in aged mouse livers regardless of gender. Taken together, our results suggest that the senescent ribosome complex appears to have low levels of rpLP1/rpLP2 and YB-1, resulting in altered translational efficiency for senescence-related genes.
机译:核糖体具有由RPLP0,RPLP1和RPLP2组成的侧向茎。当诱导细胞衰老时,这些蛋白质RPLP2中的一种蛋白质RPLP2降低。 Y型盒子结合蛋白-1(YB-1)也降低了衰老细胞的多乐组体馏分。我们发现核糖体中的RPLP2耗竭会导致多肌质中的YB-1脱离,并且它与细胞衰老有关。我们的结果还显示,在衰老细胞中递减CK2α或GRK2诱导不磷酸化的RPLP2增加,导致来自多元素的YB-I释放。这种异质衰老核糖体具有不同的衰老相关基因的平移效率。我们还表明,衰老核糖体中的RPLP1 / RPLP2和YB-1的降低不是特异性的细胞型或应力型,并且在老鼠肝脏中也观察到相同的现象,无论性别如何。我们的结果表明,衰老核糖体综合体似乎具有低水平的RPLP1 / RPLP2和YB-1,导致衰老相关基因的翻译效率改变。

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