Conserved metabolite regulation of stress granule assembly via AdoMet

被引:11
作者
Begovich, Kyle [1 ,2 ]
Vu, Anthony Q. [3 ,4 ,5 ]
Yeo, Gene [3 ,4 ,5 ]
Wilhelm, James E. [1 ,2 ]
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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页数:28
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