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DGCR8的核仁定位及11种与DGCR8相关蛋白的鉴定。

Nucleolar localization of DGCR8 and identification of eleven DGCR8-associated proteins.

作者信息

Shiohama Aiko, Sasaki Takashi, Noda Setsuko, Minoshima Shinsei, Shimizu Nobuyoshi

机构信息

Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan; GSP Center, The Leading Institute of Keio University, Ibaraki, Japan.

出版信息

Exp Cell Res. 2007 Dec 10;313(20):4196-207. doi: 10.1016/j.yexcr.2007.07.020. Epub 2007 Jul 25.

Abstract

We identified 11 proteins that are associated with DGCR8 by immunoprecipitation assay and mass spectrometry. These proteins included Nucleolin, ILF3 and others, most of which appeared to be involved in the RNA processing or RNA transportation. We detected at least four kinds of protein complex, such as DROSHA/DGCR8, DGCR8/Nucleolin, DGCR8/ILF3 and ILF3/XPO5, by co-immunoprecipitation. The complex formation of DGCR8 with Nucleolin was dependent on RNA. Subcellular localization analysis by the immunofluorescent microscopy and immunoelectron microscopy indicated that DGCR8 locates at the nucleolus and small foci adjacent to splicing speckles in the nucleoplasm. Furthermore, the localization of DGCR8 at the nucleolus was changed by the inhibition of RNA transcription. Thus, our studies provided additional new evidence for the involvement of various protein complexes in the molecular mechanisms of apparently complex innate RNA interference machinery.

摘要

我们通过免疫沉淀分析和质谱鉴定出11种与DGCR8相关的蛋白质。这些蛋白质包括核仁素、ILF3等,其中大多数似乎参与RNA加工或RNA运输。我们通过共免疫沉淀检测到至少四种蛋白质复合物,如DROSHA/DGCR8、DGCR8/核仁素、DGCR8/ILF3和ILF3/XPO5。DGCR8与核仁素的复合物形成依赖于RNA。免疫荧光显微镜和免疫电子显微镜的亚细胞定位分析表明,DGCR8定位于核仁以及核质中与剪接斑点相邻的小焦点处。此外,RNA转录的抑制改变了DGCR8在核仁中的定位。因此,我们的研究为各种蛋白质复合物参与明显复杂的先天性RNA干扰机制的分子机制提供了新的额外证据。

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