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首页> 外文期刊>Journal of cell biology >Mammalian WDR12 is a novel member of the Pes1–Bop1 complex and is required for ribosome biogenesis and cell proliferation
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Mammalian WDR12 is a novel member of the Pes1–Bop1 complex and is required for ribosome biogenesis and cell proliferation

机译:哺乳动物WDR12是Pes1-Bop1复合体的新成员,是核糖体生物发生和细胞增殖所必需的

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摘要

Target genes of the protooncogene c- myc are implicated in cell cycle and growth control, yet the linkage of both is still unexplored. Here, we show that the products of the nucleolar target genes Pes1 and Bop1 form a stable complex with a novel member, WDR12 (PeBoW complex). Endogenous WDR12, a WD40 repeat protein, is crucial for processing of the 32S precursor ribosomal RNA (rRNA) and cell proliferation. Further, a conditionally expressed dominant-negative mutant of WDR12 also blocks rRNA processing and induces a reversible cell cycle arrest. Mutant WDR12 triggers accumulation of p53 in a p19ARF-independent manner in proliferating cells but not in quiescent cells. Interestingly, a potential homologous complex of Pes1–Bop1–WDR12 in yeast (Nop7p–Erb1p–Ytm1p) is involved in the control of ribosome biogenesis and S phase entry. In conclusion, the integrity of the PeBoW complex is required for ribosome biogenesis and cell proliferation in mammalian cells.
机译:原癌基因c-myc的靶基因与细胞周期和生长控制有关,但两者之间的联系仍未探索。在这里,我们显示核仁靶基因Pes1和Bop1的产物与一个新成员WDR12(PeBoW复合物)形成稳定的复合物。内源性WDR12是WD40重复蛋白,对于32S前体核糖体RNA(rRNA)的加工和细胞增殖至关重要。此外,WDR12的条件表达显性负阴性突变体也阻断rRNA加工并诱导可逆的细胞周期停滞。突变的WDR12以p19ARF独立的方式触发p53在增殖细胞中积累,但在静止细胞中不积累。有趣的是,酵母中Pes1-Bop1-WDR12的潜在同源复合物(Nop7p-Erb1p-Ytm1p)参与了核糖体的生物发生和S期进入。总之,哺乳动物细胞中核糖体的生物发生和细胞增殖需要PeBoW复合物的完整性。

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