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      The role of survival motor neuron protein (SMN) in protein homeostasis

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          Abstract

          Ever since loss of survival motor neuron (SMN) protein was identified as the direct cause of the childhood inherited neurodegenerative disorder spinal muscular atrophy, significant efforts have been made to reveal the molecular functions of this ubiquitously expressed protein. Resulting research demonstrated that SMN plays important roles in multiple fundamental cellular homeostatic pathways, including a well-characterised role in the assembly of the spliceosome and biogenesis of ribonucleoproteins. More recent studies have shown that SMN is also involved in other housekeeping processes, including mRNA trafficking and local translation, cytoskeletal dynamics, endocytosis and autophagy. Moreover, SMN has been shown to influence mitochondria and bioenergetic pathways as well as regulate function of the ubiquitin–proteasome system. In this review, we summarise these diverse functions of SMN, confirming its key role in maintenance of the homeostatic environment of the cell.

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          Most cited references164

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          Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail.

          The canonical histone proteins are encoded by replication-dependent genes and must rapidly reach high levels of expression during S phase. In metazoans the genes that encode these proteins produce mRNAs that, instead of being polyadenylated, contain a unique 3' end structure. By contrast, the synthesis of the variant, replication-independent histones, which are encoded by polyadenylated mRNAs, persists outside of S phase. Accurate positioning of both histone types in chromatin is essential for proper transcriptional regulation, the demarcation of heterochromatic boundaries and the epigenetic inheritance of gene expression patterns. Recent results suggest that the coordinated synthesis of replication-dependent and variant histone mRNAs is achieved by signals that affect formation of the 3' end of the replication-dependent histone mRNAs.
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            Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex

            Autophagy is a membrane trafficking to vacuole/lysosome induced by nutrient starvation. In Saccharomyces cerevisiae, Tor protein, a phosphatidylinositol kinase-related kinase, is involved in the repression of autophagy induction by a largely unknown mechanism. Here, we show that the protein kinase activity of Apg1 is enhanced by starvation or rapamycin treatment. In addition, we have also found that Apg13, which binds to and activates Apg1, is hyperphosphorylated in a Tor-dependent manner, reducing its affinity to Apg1. This Apg1–Apg13 association is required for autophagy, but not for the cytoplasm-to-vacuole targeting (Cvt) pathway, another vesicular transport mechanism in which factors essential for autophagy (Apg proteins) are also employed under vegetative growth conditions. Finally, other Apg1-associating proteins, such as Apg17 and Cvt9, are shown to function specifically in autophagy or the Cvt pathway, respectively, suggesting that the Apg1 complex plays an important role in switching between two distinct vesicular transport systems in a nutrient-dependent manner.
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              SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing.

              The survival of motor neurons (SMN) protein is essential for the biogenesis of small nuclear RNA (snRNA)-ribonucleoproteins (snRNPs), the major components of the pre-mRNA splicing machinery. Though it is ubiquitously expressed, SMN deficiency causes the motor neuron degenerative disease spinal muscular atrophy (SMA). We show here that SMN deficiency, similar to that which occurs in severe SMA, has unexpected cell type-specific effects on the repertoire of snRNAs and mRNAs. It alters the stoichiometry of snRNAs and causes widespread pre-mRNA splicing defects in numerous transcripts of diverse genes, preferentially those containing a large number of introns, in SMN-deficient mouse tissues. These findings reveal a key role for the SMN complex in RNA metabolism and in splicing regulation and indicate that SMA is a general splicing disease that is not restricted to motor neurons.
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                Author and article information

                Contributors
                +44 (0)131 6503724 , t.gillingwater@ed.ac.uk
                Journal
                Cell Mol Life Sci
                Cell. Mol. Life Sci
                Cellular and Molecular Life Sciences
                Springer International Publishing (Cham )
                1420-682X
                1420-9071
                5 June 2018
                5 June 2018
                2018
                : 75
                : 21
                : 3877-3894
                Affiliations
                [1 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, Euan MacDonald Centre for Motor Neurone Disease Research, , University of Edinburgh, ; Edinburgh, UK
                [2 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, Edinburgh Medical School: Biomedical Sciences, , University of Edinburgh, ; Edinburgh, UK
                [3 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, Royal (Dick) School of Veterinary Studies, , University of Edinburgh, ; Edinburgh, UK
                Author information
                http://orcid.org/0000-0002-0306-5577
                http://orcid.org/0000-0002-4525-7059
                Article
                2849
                10.1007/s00018-018-2849-1
                6182345
                29872871
                ea0d6074-f9ab-47ae-b445-901fc8faac5b
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 26 April 2018
                : 30 May 2018
                : 31 May 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100011776, MND Scotland;
                Award ID: Project Grant
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100011708, SMA Trust;
                Award ID: UK Research Consortium
                Award Recipient :
                Funded by: SMA Europe
                Award ID: Project Grant
                Award Recipient :
                Categories
                Review
                Custom metadata
                © Springer Nature Switzerland AG 2018

                Molecular biology
                spinal muscular atrophy,ribonucleoprotein,translation,cytoskeleton,ubiquitin,bioenergetic pathway

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