Lsm7 phase-separated condensates trigger stress granule formation

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作者
Michelle Lindström
Lihua Chen
Shan Jiang
Dan Zhang
Yuan Gao
Ju Zheng
Xinxin Hao
Xiaoxue Yang
Arpitha Kabbinale
Johannes Thoma
Lisa C. Metzger
Deyuan Y. Zhang
Xuefeng Zhu
Huisheng Liu
Claes M. Gustafsson
Björn M. Burmann
Joris Winderickx
Per Sunnerhagen
Beidong Liu
机构
[1] University of Gothenburg,Department of Chemistry and Molecular Biology
[2] Guangzhou Laboratory,Wallenberg Centre for Molecular and Translational Medicine
[3] Functional Biology,College of Artificial Intelligence
[4] KU Leuven,Department of Medical Biochemistry and Cell Biology
[5] University of Gothenburg,undefined
[6] Shenyang Aerospace University,undefined
[7] Shenbei New District,undefined
[8] University of Gothenburg,undefined
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摘要
Stress granules (SGs) are non-membranous organelles facilitating stress responses and linking the pathology of age-related diseases. In a genome-wide imaging-based phenomic screen, we identify Pab1 co-localizing proteins under 2-deoxy-D-glucose (2-DG) induced stress in Saccharomyces cerevisiae. We find that deletion of one of the Pab1 co-localizing proteins, Lsm7, leads to a significant decrease in SG formation. Under 2-DG stress, Lsm7 rapidly forms foci that assist in SG formation. The Lsm7 foci form via liquid-liquid phase separation, and the intrinsically disordered region and the hydrophobic clusters within the Lsm7 sequence are the internal driving forces in promoting Lsm7 phase separation. The dynamic Lsm7 phase-separated condensates appear to work as seeding scaffolds, promoting Pab1 demixing and subsequent SG initiation, seemingly mediated by RNA interactions. The SG initiation mechanism, via Lsm7 phase separation, identified in this work provides valuable clues for understanding the mechanisms underlying SG formation and SG-associated human diseases.
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