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1
Ongoing U snRNP biogenesis is required for the integrity of Cajal bodies.持续的U snRNP生物合成是卡哈尔体完整性所必需的。
Mol Biol Cell. 2006 Jul;17(7):3221-31. doi: 10.1091/mbc.e06-03-0247. Epub 2006 May 10.
2
Depletion of SMN by RNA interference in HeLa cells induces defects in Cajal body formation.在HeLa细胞中通过RNA干扰使生存运动神经元(SMN)耗竭会导致卡哈尔体形成缺陷。
Nucleic Acids Res. 2006 May 31;34(10):2925-32. doi: 10.1093/nar/gkl374. Print 2006.
3
Residual Cajal bodies in coilin knockout mice fail to recruit Sm snRNPs and SMN, the spinal muscular atrophy gene product.卷曲螺旋蛋白基因敲除小鼠中的残留卡哈尔体无法募集Sm小核核糖核蛋白和运动神经元生存蛋白(脊髓性肌萎缩症基因产物)。
J Cell Biol. 2001 Jul 23;154(2):293-307. doi: 10.1083/jcb.200104083.
4
Detection of snRNP assembly intermediates in Cajal bodies by fluorescence resonance energy transfer.通过荧光共振能量转移检测卡哈尔体中的小核核糖核蛋白组装中间体
J Cell Biol. 2004 Sep 27;166(7):1015-25. doi: 10.1083/jcb.200405160.
5
Spliceosomal small nuclear ribonucleoprotein particles repeatedly cycle through Cajal bodies.剪接体小核核糖核蛋白颗粒反复穿梭于卡哈尔体。
Mol Biol Cell. 2008 Jun;19(6):2534-43. doi: 10.1091/mbc.e07-12-1259. Epub 2008 Mar 26.
6
snRNP protein expression enhances the formation of Cajal bodies containing p80-coilin and SMN.小核核糖核蛋白(snRNP)蛋白表达增强了含有p80-卷曲螺旋蛋白和生存运动神经元蛋白(SMN)的卡哈尔体的形成。
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7
In vivo kinetics of Cajal body components.卡哈尔体成分的体内动力学。
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8
The spinal muscular atrophy disease gene product, SMN: A link between snRNP biogenesis and the Cajal (coiled) body.脊髓性肌萎缩症疾病基因产物,SMN:小核核糖核蛋白生物合成与卡哈尔(卷曲)体之间的联系。
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The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.患者成纤维细胞卡哈尔体中snoRNP伴侣蛋白Nopp140的缺失与脊髓性肌萎缩症的严重程度相关。
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Targeting of U4/U6 small nuclear RNP assembly factor SART3/p110 to Cajal bodies.U4/U6小核核糖核蛋白组装因子SART3/p110定位于卡哈尔体。
J Cell Biol. 2003 Feb 17;160(4):505-16. doi: 10.1083/jcb.200210087. Epub 2003 Feb 10.

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SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.SNUPN 缺乏导致 RNA 剪接错误和细胞外基质失调,引起隐性肌肉营养不良。
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本文引用的文献

1
Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins.双子蛋白是Sm类核糖核蛋白高效组装所必需的。
Proc Natl Acad Sci U S A. 2005 Nov 29;102(48):17372-7. doi: 10.1073/pnas.0508947102. Epub 2005 Nov 21.
2
Cajal bodies: a long history of discovery.卡哈尔体:漫长的发现历程。
Annu Rev Cell Dev Biol. 2005;21:105-31. doi: 10.1146/annurev.cellbio.20.010403.103738.
3
Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy.U小核核糖核蛋白组装减少导致脊髓性肌萎缩动物模型中的运动轴突退化。
Genes Dev. 2005 Oct 1;19(19):2320-30. doi: 10.1101/gad.342005.
4
The C-terminal domain of coilin interacts with Sm proteins and U snRNPs.卷曲螺旋蛋白的C末端结构域与Sm蛋白和U小核核糖核蛋白相互作用。
Chromosoma. 2005 Aug;114(3):155-66. doi: 10.1007/s00412-005-0003-y. Epub 2005 Jul 8.
5
Process or perish: quality control in mRNA biogenesis.不进则退:mRNA生物合成中的质量控制
Nat Struct Mol Biol. 2005 Jun;12(6):482-8. doi: 10.1038/nsmb945.
6
Gemins modulate the expression and activity of the SMN complex.双子蛋白调节生存运动神经元复合体的表达和活性。
Hum Mol Genet. 2005 Jun 15;14(12):1605-11. doi: 10.1093/hmg/ddi168. Epub 2005 Apr 20.
7
Human splicing factor SF3a, but not SF1, is essential for pre-mRNA splicing in vivo.人剪接因子SF3a而非SF1,对体内前体mRNA剪接至关重要。
Mol Biol Cell. 2005 Mar;16(3):1366-77. doi: 10.1091/mbc.e04-11-1034. Epub 2005 Jan 12.
8
Assembly and maturation of the U3 snoRNP in the nucleoplasm in a large dynamic multiprotein complex.U3小核仁核糖核蛋白(snoRNP)在核质中通过一个大型动态多蛋白复合体进行组装和成熟。
Mol Cell. 2004 Dec 3;16(5):789-98. doi: 10.1016/j.molcel.2004.11.012.
9
PHAX and CRM1 are required sequentially to transport U3 snoRNA to nucleoli.PHAX和CRM1是将U3小核仁RNA转运至核仁所依次需要的。
Mol Cell. 2004 Dec 3;16(5):777-87. doi: 10.1016/j.molcel.2004.11.013.
10
Detection of snRNP assembly intermediates in Cajal bodies by fluorescence resonance energy transfer.通过荧光共振能量转移检测卡哈尔体中的小核核糖核蛋白组装中间体
J Cell Biol. 2004 Sep 27;166(7):1015-25. doi: 10.1083/jcb.200405160.

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.

DOI:10.1091/mbc.e06-03-0247
PMID:16687569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1483051/
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。