The function of RNA-binding proteins at the synapse: implications for neurodegeneration

作者: Chantelle F. Sephton , Gang Yu

DOI: 10.1007/S00018-015-1943-X

关键词:

摘要: The loss of synapses is a central event in neurodegenerative diseases. Synaptic proteins are often associated with disease neuropathology, but their role synaptic not fully understood. Of the many processes involved sustaining integrity synapses, local protein translation can directly impact formation, communication, and maintenance. RNA-binding association RNA granules serve to regulate mRNA transportation at turn synapse. Genetic mutations FUS TDP-43 have been linked causing diseases: amyotrophic lateral sclerosis frontotemporal dementia. observation that coincide changes provides evidence dysfunction metabolism may underlie mechanism these However, we do know how would affect granule dynamics translation, or if alterations cause neurodegeneration. Further investigation into this area will lead important insights disruption

参考文章(176)
Lei Xing, Gary J. Bassell, mRNA Localization: An Orchestration of Assembly, Traffic and Synthesis Traffic. ,vol. 14, pp. 2- 14 ,(2013) , 10.1111/TRA.12004
Gül Dölen, Mark F. Bear, Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome. The Journal of Physiology. ,vol. 586, pp. 1503- 1508 ,(2008) , 10.1113/JPHYSIOL.2008.150722
L Nover, K D Scharf, D Neumann, Cytoplasmic heat shock granules are formed from precursor particles and are associated with a specific set of mRNAs. Molecular and Cellular Biology. ,vol. 9, pp. 1298- 1308 ,(1989) , 10.1128/MCB.9.3.1298
Hitomi Tsuiji, Yohei Iguchi, Asako Furuya, Ayane Kataoka, Hiroyuki Hatsuta, Naoki Atsuta, Fumiaki Tanaka, Yoshio Hashizume, Hiroyasu Akatsu, Shigeo Murayama, Gen Sobue, Koji Yamanaka, Spliceosome integrity is defective in the motor neuron diseases ALS and SMA Embo Molecular Medicine. ,vol. 5, pp. 221- 234 ,(2013) , 10.1002/EMMM.201202303
Mariangela Morlando, Stefano Dini Modigliani, Giulia Torrelli, Alessandro Rosa, Valerio Di Carlo, Elisa Caffarelli, Irene Bozzoni, FUS stimulates microRNA biogenesis by facilitating co-transcriptional Drosha recruitment. The EMBO Journal. ,vol. 31, pp. 4502- 4510 ,(2012) , 10.1038/EMBOJ.2012.319
Jacob C. Schwartz, Xueyin Wang, Elaine R. Podell, Thomas R. Cech, RNA Seeds Higher Order Assembly of FUS Protein Cell Reports. ,vol. 5, pp. 918- 925 ,(2013) , 10.1016/J.CELREP.2013.11.017
Muriel Brengues, Daniela Teixeira, Roy Parker, Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science. ,vol. 310, pp. 486- 489 ,(2005) , 10.1126/SCIENCE.1115791
Amandine Molliex, Anderson P. Kanagaraj, Robert Carter, Kevin B. Boylan, Aleksandra M. Wojtas, Rosa Rademakers, Jack L. Pinkus, Steven A. Greenberg, John Q. Trojanowski, Bryan J. Traynor, Bradley N. Smith, Simon Topp, Athina-Soragia Gkazi, Jack Miller, Christopher E. Shaw, Michael Kottlors, Janbernd Kirschner, Alan Pestronk, Yun R. Li, Alice Flynn Ford, Aaron D. Gitler, Michael Benatar, Oliver D. King, Virginia E. Kimonis, Eric D. Ross, Conrad C. Weihl, James Shorter, J. Paul Taylor, Hong Joo Kim, Nam Chul Kim, Yong-Dong Wang, Emily A. Scarborough, Jennifer Moore, Zamia Diaz, Kyle S. MacLea, Brian Freibaum, Songqing Li, Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS Nature. ,vol. 495, pp. 467- 473 ,(2013) , 10.1038/NATURE11922
Jeffrey N. Savas, Bin Ma, Katrin Deinhardt, Brady P. Culver, Sophie Restituito, Ligang Wu, Joel G. Belasco, Moses V. Chao, Naoko Tanese, A role for Huntington disease protein in dendritic RNA granules Journal of Biological Chemistry. ,vol. 285, pp. 13142- 13153 ,(2010) , 10.1074/JBC.M110.114561