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持续的U snRNP生物合成是卡哈尔体完整性所必需的。

Ongoing U snRNP biogenesis is required for the integrity of Cajal bodies.

作者信息

Lemm Ira, Girard Cyrille, Kuhn Andreas N, Watkins Nicholas J, Schneider Marc, Bordonné Rémy, Lührmann Reinhard

机构信息

Department of Cellular Biochemistry, Max-Planck-Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.

出版信息

Mol Biol Cell. 2006 Jul;17(7):3221-31. doi: 10.1091/mbc.e06-03-0247. Epub 2006 May 10.

Abstract

Cajal bodies (CBs) have been implicated in the nuclear phase of the biogenesis of spliceosomal U small nuclear ribonucleoproteins (U snRNPs). Here, we have investigated the distribution of the CB marker protein coilin, U snRNPs, and proteins present in C/D box small nucleolar (sno)RNPs in cells depleted of hTGS1, SMN, or PHAX. Knockdown of any of these three proteins by RNAi interferes with U snRNP maturation before the reentry of U snRNA Sm cores into the nucleus. Strikingly, CBs are lost in the absence of hTGS1, SMN, or PHAX and coilin is dispersed in the nucleoplasm into numerous small foci. This indicates that the integrity of canonical CBs is dependent on ongoing U snRNP biogenesis. Spliceosomal U snRNPs show no detectable concentration in nuclear foci and do not colocalize with coilin in cells lacking hTGS1, SMN, or PHAX. In contrast, C/D box snoRNP components concentrate into nuclear foci that partially colocalize with coilin after inhibition of U snRNP maturation. We demonstrate by siRNA-mediated depletion that coilin is required for the condensation of U snRNPs, but not C/D box snoRNP components, into nucleoplasmic foci, and also for merging these factors into canonical CBs. Altogether, our data suggest that CBs have a modular structure with distinct domains for spliceosomal U snRNPs and snoRNPs.

摘要

卡哈尔体(CBs)与剪接体U小核核糖核蛋白(U snRNPs)生物合成的核阶段有关。在此,我们研究了在hTGS1、SMN或PHAX缺失的细胞中,CB标记蛋白卷曲螺旋蛋白、U snRNPs以及C/D盒小核仁(sno)RNPs中存在的蛋白质的分布情况。通过RNA干扰敲低这三种蛋白质中的任何一种,都会在U snRNA Sm核心重新进入细胞核之前干扰U snRNP的成熟。引人注目的是,在缺乏hTGS1、SMN或PHAX的情况下,CBs会消失,卷曲螺旋蛋白会分散在核质中形成许多小焦点。这表明典型CBs的完整性依赖于持续的U snRNP生物合成。在缺乏hTGS1、SMN或PHAX的细胞中,剪接体U snRNPs在核焦点中未检测到浓度,也不与卷曲螺旋蛋白共定位。相比之下,在抑制U snRNP成熟后,C/D盒snoRNP成分会浓缩成与卷曲螺旋蛋白部分共定位的核焦点。我们通过siRNA介导的缺失实验证明,卷曲螺旋蛋白是U snRNPs而非C/D盒snoRNP成分凝聚到核质焦点所必需的,也是将这些因子合并到典型CBs中所必需的。总之,我们的数据表明CBs具有模块化结构,对于剪接体U snRNPs和snoRNPs具有不同的结构域。

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