4.6 Review

SMN control of RNP assembly: From post-transcriptional gene regulation to motor neuron disease

Journal

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Volume 32, Issue -, Pages 22-29

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2014.04.026

Keywords

Spinal muscular atrophy (SMA); Survival motor neuron (SMN); Small nuclear RNA (snRNA); Ribonucleoprotein complexes (RNPs); Sm and LSm proteins; RNA processing

Funding

  1. U.S. Department of Defense [W81XWH-10-1- 0126]
  2. NIH-NINDS [NS069601, NS067448, NS079002]

Ask authors/readers for more resources

At the post-transcriptional level, expression of protein-coding genes is controlled by a series of RNA regulatory events including nuclear processing of primary transcripts, transport of mature mRNAs to specific cellular compartments, translation and ultimately, turnover. These processes are orchestrated through the dynamic association of mRNAs with RNA binding proteins and ribonucleoprotein (RNP) complexes. Accurate formation of RNPs in vivo is fundamentally important to cellular development and function, and its impairment often leads to human disease. The survival motor neuron (SMN) protein is key to this biological paradigm: SMN is essential for the biogenesis of various RNPs that function in mRNA processing, and genetic mutations leading to SMN deficiency cause the neurodegenerative disease spinal muscular atrophy. Here we review the expanding role of SMN in the regulation of gene expression through its multiple functions in RNP assembly. We discuss advances in our understanding of SMN activity as a chaperone of RNPs and how disruption of SMN-dependent RNA pathways can cause motor neuron disease. (C) 2014 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available