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Gene Expression

The Survival of Motor Neurons Protein Determines the Capacity for snRNP Assembly: Biochemical Deficiency in Spinal Muscular Atrophy

, , , , , & show all
Pages 5543-5551 | Received 14 Feb 2005, Accepted 30 Mar 2005, Published online: 27 Mar 2023
 

Abstract

Reduction of the survival of motor neurons (SMN) protein levels causes the motor neuron degenerative disease spinal muscular atrophy, the severity of which correlates with the extent of reduction in SMN. SMN, together with Gemins 2 to 7, forms a complex that functions in the assembly of small nuclear ribonucleoprotein particles (snRNPs). Complete depletion of the SMN complex from cell extracts abolishes snRNP assembly, the formation of heptameric Sm cores on snRNAs. However, what effect, if any, reduction of SMN protein levels, as occurs in spinal muscular atrophy patients, has on the capacity of cells to produce snRNPs is not known. To address this, we developed a sensitive and quantitative assay for snRNP assembly, the formation of high-salt- and heparin-resistant stable Sm cores, that is strictly dependent on the SMN complex. We show that the extent of Sm core assembly is directly proportional to the amount of SMN protein in cell extracts. Consistent with this, pulse-labeling experiments demonstrate a significant reduction in the rate of snRNP biogenesis in low-SMN cells. Furthermore, extracts of cells from spinal muscular atrophy patients have a lower capacity for snRNP assembly that corresponds directly to the reduced amount of SMN. Thus, SMN determines the capacity for snRNP biogenesis, and our findings provide evidence for a measurable deficiency in a biochemical activity in cells from patients with spinal muscular atrophy.

ACKNOWLEDGMENTS

We are grateful to Joan A. Steitz for providing the Y12 monoclonal antibody. We thank Stephen A. Liebhaber, Tracey J. Golembe, and the members of our laboratory for stimulating discussions and helpful comments on the manuscript. We are also grateful to Gina Daly for secretarial assistance.

This work was supported by the Association Française Contre les Myopathies (AFM) and by a grant from the National Institutes of Health. G.D. is an Investigator of the Howard Hughes Medical Institute.

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