Kinetic and subcellular analysis of PS-ASO/protein interactions with P54nrb and RNase H1.
Ontology highlight
ABSTRACT: The rapid RNase H1-dependent mislocalization of heterodimer proteins P54nrb and PSF to nucleoli is an early event in the pathway that explains the effects of most toxic phosphorothioate ASOs (PS-ASOs). Using a recently developed NanoLuciferace (NLuc)-based structural complementation reporter system which allows us to observe ASO/protein interactions in real time in live cells, we have determined that safe and toxic PS-ASOs associate with these proteins with kinetics and impact on subcellular localization that differ. Toxic PS-ASOs interact in a complex that includes RNase H1, P54nrb and PSF; but RNase H1/P54nrb complexes were observed in only the cells treated with toxic, but not safe PS-ASOs. In addition, experiments performed in vitro suggest that RNA is also a required component of the
SUBMITTER: Vickers TA
PROVIDER: S-EPMC6846478 | biostudies-literature | 2019 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA