TDP-43 in ALS: Stay on Target ... Almost There

被引:8
|
作者
Jovicic, Ana [1 ]
Gitler, Aaron D. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; RNA; GRANULES;
D O I
10.1016/j.neuron.2014.01.034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
ALS is associated with RNA processing impairments involving the RNA-binding protein TDP-43. Pioneering a novel RNA beacon to illuminate RNA trafficking in neurons, Alami et al. (2014) discover a cytoplasmic function for TDP-43, suggesting a new disease mechanism.
引用
收藏
页码:463 / 465
页数:3
相关论文
共 50 条
  • [21] ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS
    Ling, Shuo-Chien
    Albuquerque, Claudio P.
    Han, Joo Seok
    Lagier-Tourenne, Clotilde
    Tokunaga, Seiya
    Zhou, Huilin
    Cleveland, Don W.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (30) : 13318 - 13323
  • [22] Phosphorylated TDP-43 becomes resistant to cleavage by calpain: A regulatory role for phosphorylation in TDP-43 pathology of ALS/FTLD
    Yamashita, Takenari
    Teramoto, Sayaka
    Kwak, Shin
    NEUROSCIENCE RESEARCH, 2016, 107 : 63 - 69
  • [23] Spreading of TDP-43 pathology via pyramidal tract induces ALS-like phenotypes in TDP-43 transgenic mice
    Ding, Xuebing
    Xiang, Zhi
    Qin, Chi
    Chen, Yongkang
    Tian, Haiyan
    Meng, Lin
    Xia, Danhao
    Liu, Han
    Song, Jia
    Fu, Jun
    Ma, Mingming
    Wang, Xuejing
    ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2021, 9 (01)
  • [24] Small-Molecule Modulation of TDP-43 Recruitment to Stress Granules Prevents Persistent TDP-43 Accumulation in ALS/FTD
    Fang, Mark Y.
    Markmiller, Sebastian
    Vu, Anthony Q.
    Javaherian, Ashkan
    Dowdle, William E.
    Jolivet, Philippe
    Bushway, Paul J.
    Castello, Nicholas A.
    Baral, Ashmita
    Chan, Michelle Y.
    Linsley, Jeremy W.
    Linsley, Drew
    Mercola, Mark
    Finkbeiner, Steven
    Lecuyer, Eric
    Lewcock, Joseph W.
    Yeo, Gene W.
    NEURON, 2019, 103 (05) : 802 - +
  • [25] Spreading of TDP-43 pathology via pyramidal tract induces ALS-like phenotypes in TDP-43 transgenic mice
    Xuebing Ding
    Zhi Xiang
    Chi Qin
    Yongkang Chen
    Haiyan Tian
    Lin Meng
    Danhao Xia
    Han Liu
    Jia Song
    Jun Fu
    Mingming Ma
    Xuejing Wang
    Acta Neuropathologica Communications, 9
  • [26] TDP-43 Cytoplasmic Translocation in the Skin Fibroblasts of ALS Patients
    Rubio, Miguel A.
    Herrando-Grabulosa, Mireia
    Velasco, Roser
    Blasco, Israel
    Povedano, Monica
    Navarro, Xavier
    CELLS, 2022, 11 (02)
  • [27] Understanding the role of TDP-43 and FUS/TLS in ALS and beyond
    Da Cruz, Sandrine
    Cleveland, Don W.
    CURRENT OPINION IN NEUROBIOLOGY, 2011, 21 (06) : 904 - 919
  • [28] Structure of pathological TDP-43 filaments from ALS with FTLD
    Arseni, Diana
    Hasegawa, Masato
    Murzin, Alexey G.
    Kametani, Fuyuki
    Arai, Makoto
    Yoshida, Mari
    Ryskeldi-Falcon, Benjamin
    NATURE, 2022, 601 (7891) : 139 - +
  • [29] Developing RNA therapeutics for TDP-43 proteinopathy in ALS/FTD
    Copley, Katie
    Smirnov, Ashleigh
    Mayne, Leland
    Wang, Yuanhang
    Black, Ben E.
    Shorter, James
    BIOPHYSICAL JOURNAL, 2024, 123 (03) : 485A - 486A
  • [30] An ALS-mutant TDP-43 neurotoxic peptide adopts an anti-parallel β-structure and induces TDP-43 redistribution
    Zhu, Li
    Xu, Meng
    Yang, Mengxue
    Yang, Yanlian
    Li, Yang
    Deng, Jianwen
    Ruan, Linhao
    Liu, Jianghong
    Du, Sidan
    Liu, Xuehui
    Feng, Wei
    Fushimi, Kazuo
    Bigio, Eileen H.
    Mesulam, Marsel
    Wang, Chen
    Wu, Jane Y.
    HUMAN MOLECULAR GENETICS, 2014, 23 (25) : 6863 - 6877