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Conserved metabolite regulation of stress granule assembly via AdoMet
被引:11
作者:

Begovich, Kyle
论文数: 0 引用数: 0
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机构:
Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA
Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA

Vu, Anthony Q.
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h-index: 0
机构:
Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
Univ Calif San Diego, Stem Cell Program, La Jolla, CA 92093 USA
Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA

Yeo, Gene
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
Univ Calif San Diego, Stem Cell Program, La Jolla, CA 92093 USA
Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA

Wilhelm, James E.
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h-index: 0
机构:
Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA
Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA
机构:
[1] Marine Biol Lab, Summer Inst, Howard Hughes Med Inst, Woods Hole, MA 02543 USA
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Stem Cell Program, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
基金:
美国国家卫生研究院;
关键词:
S-ADENOSYLMETHIONINE SYNTHETASE;
AMYOTROPHIC-LATERAL-SCLEROSIS;
BIFUNCTIONAL ACTIVE-SITE;
DNA-BINDING PROTEIN;
PHASE-SEPARATION;
SACCHAROMYCES-CEREVISIAE;
LIQUID DROPLETS;
RNA;
FUS;
MUTATIONS;
D O I:
10.1083/jcb.201904141
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Stress granules (SGs) are evolutionarily conserved condensates of ribonucleoproteins that assemble in response to metabolic stresses. Because aberrant SG formation is associated with amyotrophic lateral sclerosis (ALS), understanding the connection between metabolic activity and SG composition can provide therapeutic insights into neurodegeneration. Here, we identify 17 metabolic enzymes recruited to yeast SGs in response to physiological growth stress. Furthermore, the product of one of these enzymes, AdoMet, is a regulator of SG assembly and composition. Decreases in AdoMet levels increase SG formation, while chronic elevation of AdoMet produces SG remnants lacking proteins associated with the 5' end of transcripts. Interestingly, acute elevation of AdoMet blocks SG formation in yeast and motor neurons. Treatment of ALS-derived motor neurons with AdoMet also suppresses the formation of TDP-43-positive SGs, a hallmark of ALS. Together, these results argue that AdoMet is an evolutionarily conserved regulator of SG composition and assembly with therapeutic potential in neurodegeneration.
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