Stress granules as crucibles of ALS pathogenesis.
Stress granules as crucibles of ALS pathogenesis.
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DOI:
10.1083/jcb.201302044
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发表时间:
2013-04-29
期刊:
影响因子:
--
通讯作者:
Gitler AD
中科院分区:
文献类型:
--
作者:
Li YR;King OD;Shorter J;Gitler AD
Amyotrophic lateral sclerosis (ALS) is a fatal human neurodegenerative disease affecting primarily motor neurons. Two RNA-binding proteins, TDP-43 and FUS, aggregate in the degenerating motor neurons of ALS patients, and mutations in the genes encoding these proteins cause some forms of ALS. TDP-43 and FUS and several related RNA-binding proteins harbor aggregation-promoting prion-like domains that allow them to rapidly self-associate. This property is critical for the formation and dynamics of cellular ribonucleoprotein granules, the crucibles of RNA metabolism and homeostasis. Recent work connecting TDP-43 and FUS to stress granules has suggested how this cellular pathway, which involves protein aggregation as part of its normal function, might be coopted during disease pathogenesis.
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