Bence György Gombás, Erika Gábor, Viktor Honti, Orsolya Németh-Szatmári, Ferenc Jankovics, Zoltán Villányi
Assemblysomes are ribosome-nascent chain condensates that regulate co-translational processes through liquid-liquid phase separation, yet the sequence determinants underlying their formation remain incompletely understood. Previous studies identified the DNA helicase Sgs1 as an assemblysome-associated protein; however, whether its N-terminal region possesses intrinsic phase separation propensity has not been experimentally examined. Here, we investigated the first 135 amino acids of Sgs1 using a light-inducible optoDroplet assay. A mCherry-Cry2-Sgs11-135 fusion construct was compared with the established positive control FUS-mCherry-Cry2 and the negative control mCherry-Cry2 in live HEK293T cells. Following blue-light activation, Sgs11-135 reproducibly formed reversible condensates, indicating intrinsic phase separation propensity. Quantitative image analysis revealed light-dependent increases in condensate number, average condensate area, and integrated condensate fluorescence intensity. Compared with FUS, Sgs11-135 formed slightly fewer and smaller condensates but displayed reproducible light-dependent condensate formation. These findings indicate that the Sgs1 N-terminal region exhibits intrinsic phase separation propensity in a validated optogenetic assay. Although this proof-of-principle study does not establish the molecular mechanism of assemblysome formation, the results are consistent with the hypothesis that the Sgs1 N-terminus may contribute to the multivalent interactions underlying assemblysome organization.