Aspergillus SUMOylation mutants have normal dynein function but exhibit chromatin bridges

• Published in: bioRxiv
• Main Authors: Zhang, Jun, Qiu, Rongde, Bieger, Baronger D, Oakley, C Elizabeth, Oakley, Berl R, Egan, Martin J, Xiang, Xin
• Format: Journal Article
• Language: English
• Published: United States 17.04.2023
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2023.04.16.537086

Functions of protein SUMOylation remain incompletely understood in different cell types. The budding yeast SUMOylation machinery interacts with LIS1, a protein critical for dynein activation, but dynein-pathway components were not identified as SUMO-targets in the filamentous fungus . Via forward genetics, here we identified *, a loss-of-function mutation in a SUMO-activation enzyme UbaB. Colonies of the *, Δ and Δ mutants looked similar and less healthy than the wild-type colony. In these mutants, about 10% of nuclei are connected by abnormal chromatin bridges, indicating the importance of SUMOylation in the completion of chromosome segregation. Nuclei connected by chromatin bridges are mostly in interphase, suggesting that these bridges do not prevent cell-cycle progression. UbaB-GFP localizes to interphase nuclei just like the previously studied SumO-GFP, but the nuclear signals disappear during mitosis when the nuclear pores are partially open, and the signals reappear after mitosis. The nuclear localization is consistent with many SUMO-targets being nuclear proteins, for example, topoisomerase II whose SUMOylation defect gives rise to chromatin bridges in mammalian cells. Unlike in mammalian cells, however, loss of SUMOylation in does not apparently affect the metaphase-to-anaphase transition, further highlighting differences in the requirements of SUMOylation in different cell types. Finally, loss of UbaB or SumO does not affect dynein- and LIS1-mediated early-endosome transport, indicating that SUMOylation is unnecessary for dynein or LIS1 function in .