Journal article

Prion-like domains in RNA binding proteins are essential for building subnuclear paraspeckles

S Hennig, G Kong, T Mannen, A Sadowska, S Kobelke, A Blythe, GJ Knott, SS Iyer, D Ho, EA Newcombe, K Hosoki, N Goshima, T Kawaguchi, D Hatters, L Trinkle-Mulcahy, T Hirose, CS Bond, AH Fox

Journal of Cell Biology | ROCKEFELLER UNIV PRESS | Published : 2015

Abstract

Prion-like domains (PLDs) are low complexity sequences found in RNA binding proteins associated with the neurodegenerative disorder amyotrophic lateral sclerosis. Recently, PLDs have been implicated in mediating gene regulation via liquid-phase transitions that drive ribonucleoprotein granule assembly. In this paper, we report many PLDs in proteins associated with paraspeckles, subnuclear bodies that form around long noncoding RNA. We mapped the interactome network of paraspeckle proteins, finding enrichment of PLDs. We show that one protein, RBM14, connects key paraspeckle subcomplexes via interactions mediated by its PLD. We further show that the RBM14 PLD, as well as the PLD of another es..

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University of Melbourne Researchers

Grants

Awarded by Japan Society for the Promotion of Science


Funding Acknowledgements

This research was supported by a Deutscher Akademischer Austauschdienst (DAAD) Fellowship to S. Hennig, Cancer Council of Western Australia Fellowship to A.H. Fox, Ministry of education, culture, sports, science and technology Grant (of Japan) 26113002 to T. Hirose, and National Health and Medical Research Council (of Australia) grants 1030695 and 1050585 to A.H. Fox and C.S. Bond.