Informace o publikaci

Multiprotein bridging factor 1 is required for robust activation of the integrated stress response on collided ribosomes

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KIM Kyusik Q. LI Jeffrey J. URS NANJARAJ Ankanahalli N. PACHECO Miguel E. LASEHINDE Victor DENK Timo TĚŠINA Petr TOMOMATSU Shota MATSUO Yoshitaka MCDONALD Elesa BECKMANN Roland INADA Toshifumi GREEN Rachel ZAHER Hani S.

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj MOLECULAR CELL
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://www.sciencedirect.com/science/article/pii/S1097276524008694?via%3Dihub
Doi http://dx.doi.org/10.1016/j.molcel.2024.10.029
Klíčová slova Gcn2; Gcn4; Mbf1; integrated stress response; ribosome; ribosome collisions; translation
Přiložené soubory
Popis In yeast, multiprotein bridging factor 1 (Mbf1) has been proposed to function in the integrated stress response (ISR) as a transcriptional coactivator by mediating a direct interaction between general transcription machinery and the process's key effector, Gcn4. However, mounting evidence has demonstrated that Mbf1 (and its human homolog EDF1) is recruited to collided ribosomes, a known activator of the ISR. In this study, we connect these otherwise seemingly disparate functions of Mbf1. Our biochemical and structural analyses reveal that Mbf1 functions as a core ISR factor by interacting with collided ribosomes to mediate Gcn2 activation. We further show that Mbf1 serves no role as a transcriptional coactivator of Gcn4. Instead, Mbf1 is required for optimal stress-induced eukaryotic initiation factor 2alpha (eIF2alpha) phosphorylation and downstream de-repression of GCN4 translation. Collectively, our data establish that Mbf1 functions in ISR signaling by acting as a direct sensor of stress-induced ribosome collisions.
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