Ro ribonucleoprotein assembly in vitro: identification of RNA-protein and protein-protein interactions

RL Slobbe, W Pluk, WJ Van Venrooij… - Journal of molecular …, 1992 - Elsevier
RL Slobbe, W Pluk, WJ Van Venrooij, GJM Pruijn
Journal of molecular biology, 1992Elsevier
The human Y RNAs, small RNAs with an unknown function, are complexed with at least
three proteins: the 60,000 M r Ro protein (Ro60), the 52,000 M r Ro protein (Ro52) and the
La protein (La). In this study we examined the intermolecular interactions between the
components of these so-called Ro ribonucleoprotein (Ro RNP) complexes. Incubation of 32
P-labelled hY1 RNA in HeLa S100 extract allows the reconstitution of Ro RNP complexes,
which were analysed by immunoprecipitation with monospecific antisera. By …
Abstract
The human Y RNAs, small RNAs with an unknown function, are complexed with at least three proteins: the 60,000 Mr Ro protein (Ro60), the 52,000 Mr Ro protein (Ro52) and the La protein (La). In this study we examined the intermolecular interactions between the components of these so-called Ro ribonucleoprotein (Ro RNP) complexes.
Incubation of 32P-labelled hY1 RNA in HeLa S100 extract allows the reconstitution of Ro RNP complexes, which were analysed by immunoprecipitation with monospecific antisera. By immunodepletion of HeLa S100 extracts for either Ro60, Ro52 or La, followed by supplementation with recombinant Ro60 or La, it was demonstrated that both Ro60 and La bind to hY1 RNA directly without being influenced by one of the other proteins. However, binding of Ro52 to hY1 RNA required the presence of Ro60, which strongly suggests that the association of Ro52 with Ro RNPs is mediated by protein-protein interactions between Ro60 and Ro52.
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