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

Authors :
Marie-Christine Rio
Marie-Pierre Chenard
Edouard Bertrand
Sébastien Degot
Hervé Le Hir
Catherine Tomasetto
Aurélie Baguet
Pascal Kessler
Corinne Wendling
Nicolas Cougot
Institut de Génétique Moléculaire de Montpellier (IGMM)
Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)
Institut de génétique et biologie moléculaire et cellulaire (IGBMC)
Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Centre de génétique moléculaire (CGM)
Centre National de la Recherche Scientifique (CNRS)
Laboratoire de Biologie structurale
Institut National de la Santé et de la Recherche Médicale (INSERM)
Institut de Génétique Moléculaire de Montpellier ( IGMM )
Université de Montpellier ( UM ) -Centre National de la Recherche Scientifique ( CNRS )
Institut de génétique et biologie moléculaire et cellulaire ( IGBMC )
Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS )
Centre de génétique moléculaire ( CGM )
Centre National de la Recherche Scientifique ( CNRS )
Biologie moléculaire et génie génétique ( IGBMC )
Institut National de la Santé et de la Recherche Médicale ( INSERM )
Biologie moléculaire et génie génétique (IGBMC)
Source :
Journal of Cell Science, Journal of Cell Science, Company of Biologists, 2007, 120 (Pt 16), pp.2774-84. ⟨10.1242/jcs.009225⟩, Journal of Cell Science, Company of Biologists, 2007, 120 (Pt 16), pp.2774-84. 〈10.1242/jcs.009225〉
Publication Year :
2007
Publisher :
HAL CCSD, 2007.

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.

Details

Language :
English
ISSN :
00219533 and 14779137
Database :
OpenAIRE
Journal :
Journal of Cell Science, Journal of Cell Science, Company of Biologists, 2007, 120 (Pt 16), pp.2774-84. ⟨10.1242/jcs.009225⟩, Journal of Cell Science, Company of Biologists, 2007, 120 (Pt 16), pp.2774-84. 〈10.1242/jcs.009225〉
Accession number :
edsair.doi.dedup.....c4ec26339783f676bb7a1c57d4e082a3
Full Text :
https://doi.org/10.1242/jcs.009225⟩