Abstract
Coilin is the signature protein of the Cajal body (CB), a nuclear suborganelle involved in the biogenesis of small nuclear ribonucleoproteins (snRNPs). Newly imported Sm-class snRNPs are thought to traffic through CBs before proceeding to their final nuclear destinations. Loss of coilin function in mice leads to significant viability and fertility problems. Coilin interacts directly with the spinal muscular atrophy (SMA) protein via dimethylarginine residues in its C-terminal domain. Although coilin hypomethylation results in delocalization of survival of motor neurons (SMN) from CBs, high concentrations of snRNPs remain within these structures. Thus, CBs appear to be involved in snRNP maturation, but factors that tether snRNPs to CBs have not been described. In this report, we demonstrate that the coilin C-terminal domain binds directly to various Sm and Lsm proteins via their Sm motifs. We show that the region of coilin responsible for this binding activity is separable from that which binds to SMN. Interestingly, U2, U4, U5, and U6 snRNPs interact with the coilin C-terminal domain in a glutathione S-transferase (GST)-pulldown assay, whereas U1 and U7 snRNPs do not. Thus, the ability to interact with free Sm (and Lsm) proteins as well as with intact snRNPs, indicates that coilin and CBs may facilitate the modification of newly formed snRNPs, the regeneration of ‘mature’ snRNPs, or the reclamation of unassembled snRNP components.
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Acknowledgements
We thank R. Lührmann, C.L. Will, and H. Salz for providing us with reagents used in this work. Moreover, we acknowledge financial support by the Novartis Foundation, the State of Bern, the Swiss National Science Foundation, the Muscular Dystrophy Association of the USA, and the US National Institutes of Health (R01 grants GM53034 and NS41617).
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Xu, H., Pillai, R.S., Azzouz, T.N. et al. The C-terminal domain of coilin interacts with Sm proteins and U snRNPs. Chromosoma 114, 155–166 (2005). https://doi.org/10.1007/s00412-005-0003-y
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DOI: https://doi.org/10.1007/s00412-005-0003-y