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首页> 外文期刊>Biochemical and Biophysical Research Communications >NVL2, a nucleolar AAA-ATPase, is associated with the nuclear exosome and is involved in pre-rRNA processing
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NVL2, a nucleolar AAA-ATPase, is associated with the nuclear exosome and is involved in pre-rRNA processing

机译:NVL2是一种核仁AAA-ATPase,与核外泌体相关,并参与rRNA的前加工

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摘要

Nuclear VCP-like 2 (NVL2) is a member of the chaperone-like AAA-ATPase family and is involved in the biosynthesis of 60S ribosomal subunits in mammalian cells. We previously showed the interaction of NVL2 with a DExD/H-box RNA helicase MTR4/DOB1, which is a known cofactor for an exoribonuclease complex, the exosome. This finding implicated NVL2 in RNA metabolic processes during ribosome biogenesis. In the present study, we found that a series of mutations within the ATPase domain of NVL2 causes a defect in pre-rRNA processing into mature 285 and 5.85 rRNAs. Co-immunoprecipitation analysis showed that NVL2 was associated with the nuclear exosome complex, which includes RRP6 as a nucleus-specific catalytic subunit. This interaction was prevented by depleting either MTR4 or RRP6, indicating their essential role in mediating this interaction with NVL2. Additionally, knockdown of MPP6, another cofactor for the nuclear exosome, also prevented the interaction by causing MTR4 to dissociate from the nuclear exosome. These results suggest that NVL2 is involved in pre-rRNA processing by associating with the nuclear exosome complex and that MPP6 is required for maintaining the integrity of this rRNA processing complex. (C) 2015 Elsevier Inc. All rights reserved.
机译:核VCP样2(NVL2)是分子伴侣AAA-ATPase家族的一员,参与哺乳动物细胞中60S核糖体亚基的生物合成。我们先前显示了NVL2与DExD / H-box RNA解旋酶MTR4 / DOB1的相互作用,MTR4 / DOB1是外切核糖核酸酶复合物外泌体的已知辅助因子。这一发现牵涉到NVL2在核糖体生物发生过程中的RNA代谢过程中。在本研究中,我们发现NVL2的ATPase域内发生一系列突变,导致pre-rRNA加工成成熟的285和5.85 rRNA时出现缺陷。免疫共沉淀分析表明NVL2与核外泌体复合体相关,该复合体包括RRP6作为核特异性催化亚基。耗尽MTR4或RRP6可以阻止这种相互作用,表明它们在介导与NVL2的相互作用中起着至关重要的作用。另外,敲除MPP6(核外泌体的另一个辅因子)也通过引起MTR4从核外泌体解离来阻止相互作用。这些结果表明,NVL2通过与核外泌体复合物结合而参与了rRNA的前加工过程,而MPP6是维持该rRNA加工复合物完整性所必需的。 (C)2015 Elsevier Inc.保留所有权利。

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