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首页> 外文期刊>Genes to cells : >Delta Np63 alpha controls YB-1 protein stability: evidence on YB-1 as a new player in keratinocyte differentiation
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Delta Np63 alpha controls YB-1 protein stability: evidence on YB-1 as a new player in keratinocyte differentiation

机译:Delta Np63 alpha控制YB-1蛋白的稳定性:YB-1作为角质形成细胞分化的新参与者的证据

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摘要

Y-box binding protein 1 (YBX-1 or YB-1) is an oncoprotein that promotes replicative immortality, tumor cell invasion and metastasis. The increase in the abundance of YB-1 in the cell or YB-1 translocation from the cytoplasm to the nucleus is characteristic of malignant cell growth. We have previously reported that Delta Np63 alpha, a transcription factor that is known to play a pivotal role in keratinocyte proliferation and differentiation, promotes YB-1 nuclear accumulation. Here, we show that YB-1 is highly expressed in proliferating keratinocytes and is down-regulated during keratinocyte differentiation. Delta Np63 alpha reduces YB-1 protein turnover and leads to accumulation of ubiquitin-conjugated YB-1 into the nucleus. Reduction of YB-1 protein level, following treatment with a DNA-damaging agent, is inhibited by DNp63a suggesting that YB-1 and Delta Np63 alpha interplay can support keratinocyte proliferation and protect cells from apoptosis under genotoxic stress.
机译:Y-box结合蛋白1(YBX-1或YB-1)是一种癌蛋白,可促进复制永生,肿瘤细胞侵袭和转移。细胞中YB-1丰度的增加或从细胞质到细胞核的YB-1转运是恶性细胞生长的特征。我们以前曾报道过,Delta Np63 alpha是一种转录因子,已知在角质形成细胞增殖和分化中起关键作用,可促进YB-1核积累。在这里,我们显示YB-1在增殖的角质形成细胞中高度表达,并在角质形成细胞分化过程中被下调。 Delta Np63α减少了YB-1蛋白的转化并导致泛素结合的YB-1积累到细胞核中。 DNp63a抑制DNA损伤剂处理后YB-1蛋白水平的降低,这表明YB-1和Delta Np63α的相互作用可以支持角质形成细胞增殖,并在基因毒性胁迫下保护细胞免受凋亡。

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