survival motor neuron;
spinal muscular atrophy;
stress granule;
TIA-l/R;
D O I:
10.1016/j.febslet.2004.07.010
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We report here that SMN co-localizes with TIA-1/R and G3BP, protein assemblers of stress granules (SGs), and that SMN is co-immunoprecipitated with TIA-1/R, suggesting that SMN granules are SGs. Formation of SMN granules precedes accumulation of TIA-1/R, indicating that SMN serves as a facilitator of SG formation. However, the exon 7 skipping product, SMNDelta7, is largely retained in the nucleus and forms nuclear granules, indicating that exon 7 is critical for SG formation. Our findings reveal a novel SMN function and possible SG involvement in the pathogenesis of spinal muscular atrophy. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
机构:
Univ Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USAUniv Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USA
Hua, YM
;
Zhou, JH
论文数: 0引用数: 0
h-index: 0
机构:
Univ Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USAUniv Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USA
机构:
Univ Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USAUniv Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USA
Hua, YM
;
Zhou, JH
论文数: 0引用数: 0
h-index: 0
机构:
Univ Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USAUniv Massachusetts, Sch Med, Dept Med, Program Neurosci, Worcester, MA 01605 USA