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外显子连接复合体组分转移淋巴结51在应激颗粒组装中发挥作用。

The exon-junction-complex-component metastatic lymph node 51 functions in stress-granule assembly.

作者信息

Baguet Aurélie, Degot Sébastien, Cougot Nicolas, Bertrand Edouard, Chenard Marie-Pierre, Wendling Corinne, Kessler Pascal, Le Hir Hervé, Rio Marie-Christine, Tomasetto Catherine

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département de Biologie du Cancer, UMR 7104 CNRS/U596 INSERM/Université Louis Pasteur, BP 10142, 67404 Illkirch, C.U. de Strasbourg, France.

出版信息

J Cell Sci. 2007 Aug 15;120(Pt 16):2774-84. doi: 10.1242/jcs.009225. Epub 2007 Jul 24.

Abstract

Metastatic lymph node 51 [MLN51 (also known as CASC3)] is a component of the exon junction complex (EJC), which is assembled on spliced mRNAs and plays important roles in post-splicing events. The four proteins of the EJC core, MLN51, MAGOH, Y14 and EIF4AIII shuttle between the cytoplasm and the nucleus. However, unlike the last three, MLN51 is mainly detected in the cytoplasm, suggesting that it plays an additional function in this compartment. In the present study, we show that MLN51 is recruited into cytoplasmic aggregates known as stress granules (SGs) together with the SG-resident proteins, fragile X mental retardation protein (FMRP), poly(A) binding protein (PABP) and poly(A)(+) RNA. MLN51 specifically associates with SGs via its C-terminal region, which is dispensable for its incorporation in the EJC. MLN51 does not promote SG formation but its silencing, or the overexpression of a mutant lacking its C-terminal region, alters SG assembly. Finally, in human breast carcinomas, MLN51 is sometimes present in cytoplasmic foci also positive for FMRP and PABP, suggesting that SGs formation occurs in malignant tumours.

摘要

转移淋巴结51 [MLN51(也称为CASC3)]是外显子连接复合体(EJC)的一个组成部分,该复合体组装在剪接后的mRNA上,并在剪接后事件中发挥重要作用。EJC核心的四种蛋白质,即MLN51、MAGOH、Y14和EIF4AIII在细胞质和细胞核之间穿梭。然而,与后三种蛋白质不同,MLN51主要在细胞质中被检测到,这表明它在这个区室中发挥额外的功能。在本研究中,我们发现MLN51与应激颗粒(SGs)中的驻留蛋白、脆性X智力低下蛋白(FMRP)、聚腺苷酸结合蛋白(PABP)和聚腺苷酸(+)RNA一起被募集到称为应激颗粒(SGs)的细胞质聚集体中。MLN51通过其C末端区域与SGs特异性结合,该区域对于其整合到EJC中是可有可无的。MLN51不促进SGs的形成,但其沉默或缺乏C末端区域突变体的过表达会改变SGs的组装。最后,在人类乳腺癌中有时也存在MLN51,其在细胞质灶中也为FMRP和PABP阳性,这表明SGs的形成发生在恶性肿瘤中。

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