Acetic acid induces proteasome storage granule formation and inhibits proteasomal proteolysis: Comparison with other induction conditions

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Authors: Mitsuki Imajo, Shoei Tanaka, Vo Thi Anh Nguyet, Mieko Hayashi, Akira Matsuura, Shingo Izawa
Cited by: 1
References: 97

Abstract

Proteasomes are primarily located within the nuclei of proliferating cells; however, their localization changes dynamically in response to environmental conditions. Saccharomyces cerevisiae forms proteasome storage granules (PSGs) in the cytoplasm upon glucose depletion, mitochondrial stress, or transition to quiescence. Although intracellular acidification drives PSG formation, the detailed mechanisms underlying this process are unclear. As the established PSG induction conditions are limited to the three conditions mentioned above, identifying other induction conditions will elucidate these mechanisms. The current study showed that acetic acid stress induced PSG formation more rapidly than other PSG induction conditions following the formation of nuclear proteasome condensates. Acetic acid inhibited proteasomal proteolysis, leading to the accumulation of ubiquitinated proteins. Of the non-essential proteasome subunits, Sem1/Dss1 was crucial, but Pre9 was less important for PSG formation under all conditions. The necessity of Rpn10 and Rpn13 for PSG formation differed depending on induction conditions. The proteasome shuttle factors, Dsk2 and Rad23, colocalized with all PSGs but were not essential for PSG formation caused by acetic acid or glucose depletion. The contributions of Hul5, an E3 ubiquitin ligase, and new protein synthesis to PSG formation also differed among the conditions, indicating that the key factors for PSG formation varied among the different induction conditions. These findings provide novel insights into the physiological effects of acetic acid on proteasomes and PSG-formation mechanisms.

Fields of Study & Subjects

Ubiquitin and proteasome pathways Microtubule and mitosis dynamics Endoplasmic Reticulum Stress and Disease

Publication details

Journal / source
Journal of Biological Chemistry
Publisher
Elsevier BV
Volume
302
Issue
4
Pages
111297–111297
Publication date
17 February 2026
Language
EN