Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons

被引:0
|
作者
Wen-Yuan Wang
Ling Pan
Susan C Su
Emma J Quinn
Megumi Sasaki
Jessica C Jimenez
Ian R A Mackenzie
Eric J Huang
Li-Huei Tsai
机构
[1] Picower Institute for Learning and Memory,Department of Brain and Cognitive Sciences
[2] Massachusetts Institute of Technology,Department of Pathology
[3] Howard Hughes Medical Institute,Department of Pathology
[4] University of British Columbia,undefined
[5] University of California San Francisco,undefined
[6] Pathology Service,undefined
[7] VA Medical Center,undefined
来源
Nature Neuroscience | 2013年 / 16卷
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摘要
Fused-in-Sarcoma (FUS) gene encodes an RNA/DNA binding protein whose mutations are linked to amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). This study shows that FUS functions in the neuronal DNA damage response by its recruitment to the site of DNA double-stranded breaks and by its interaction with histone deacetylase 1. The study also shows ALS/FTLD-associated mutant FUS is defective in DNA repair mechanism and that ALS/FTLD patients with FUS mutations have greater DNA damage.
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页码:1383 / 1391
页数:8
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