Literature DB >> 24769255

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

Darrick K Li1, Sarah Tisdale1, Francesco Lotti1, Livio Pellizzoni2.   

Abstract

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.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

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

Mesh:

Substances:

Year:  2014        PMID: 24769255      PMCID: PMC4110182          DOI: 10.1016/j.semcdb.2014.04.026

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  72 in total

1.  Evolution of an RNP assembly system: a minimal SMN complex facilitates formation of UsnRNPs in Drosophila melanogaster.

Authors:  Matthias Kroiss; Jörg Schultz; Julia Wiesner; Ashwin Chari; Albert Sickmann; Utz Fischer
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-10       Impact factor: 11.205

2.  An assembly chaperone collaborates with the SMN complex to generate spliceosomal SnRNPs.

Authors:  Ashwin Chari; Monika M Golas; Michael Klingenhäger; Nils Neuenkirchen; Bjoern Sander; Clemens Englbrecht; Albert Sickmann; Holger Stark; Utz Fischer
Journal:  Cell       Date:  2008-10-31       Impact factor: 41.582

3.  The eukaryotic genome as an RNA machine.

Authors:  Paulo P Amaral; Marcel E Dinger; Tim R Mercer; John S Mattick
Journal:  Science       Date:  2008-03-28       Impact factor: 47.728

4.  KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.

Authors:  Helina Tadesse; Julie Deschênes-Furry; Sophie Boisvenue; Jocelyn Côté
Journal:  Hum Mol Genet       Date:  2007-11-12       Impact factor: 6.150

Review 5.  Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail.

Authors:  William F Marzluff; Eric J Wagner; Robert J Duronio
Journal:  Nat Rev Genet       Date:  2008-11       Impact factor: 53.242

6.  SMN-independent subunits of the SMN complex. Identification of a small nuclear ribonucleoprotein assembly intermediate.

Authors:  Daniel J Battle; Mumtaz Kasim; Jin Wang; Gideon Dreyfuss
Journal:  J Biol Chem       Date:  2007-07-19       Impact factor: 5.157

Review 7.  Chaperoning ribonucleoprotein biogenesis in health and disease.

Authors:  Livio Pellizzoni
Journal:  EMBO Rep       Date:  2007-04       Impact factor: 8.807

8.  Gemin8 is required for the architecture and function of the survival motor neuron complex.

Authors:  Claudia Carissimi; Luciano Saieva; Francesca Gabanella; Livio Pellizzoni
Journal:  J Biol Chem       Date:  2006-10-05       Impact factor: 5.157

9.  Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs.

Authors:  Francesca Gabanella; Matthew E R Butchbach; Luciano Saieva; Claudia Carissimi; Arthur H M Burghes; Livio Pellizzoni
Journal:  PLoS One       Date:  2007-09-26       Impact factor: 3.240

10.  SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing.

Authors:  Zhenxi Zhang; Francesco Lotti; Kimberly Dittmar; Ihab Younis; Lili Wan; Mumtaz Kasim; Gideon Dreyfuss
Journal:  Cell       Date:  2008-05-16       Impact factor: 41.582

View more
  77 in total

Review 1.  The pathogenicity of splicing defects: mechanistic insights into pre-mRNA processing inform novel therapeutic approaches.

Authors:  Elisabeth Daguenet; Gwendal Dujardin; Juan Valcárcel
Journal:  EMBO Rep       Date:  2015-11-13       Impact factor: 8.807

2.  Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA.

Authors:  Chitra C Iyer; Vicki L McGovern; Jason D Murray; Sara E Gombash; Phillip G Zaworski; Kevin D Foust; Paul M L Janssen; Arthur H M Burghes
Journal:  Hum Mol Genet       Date:  2015-08-13       Impact factor: 6.150

3.  The Survival of Motor Neuron Protein Acts as a Molecular Chaperone for mRNP Assembly.

Authors:  Paul G Donlin-Asp; Claudia Fallini; Jazmin Campos; Ching-Chieh Chou; Megan E Merritt; Han C Phan; Gary J Bassell; Wilfried Rossoll
Journal:  Cell Rep       Date:  2017-02-14       Impact factor: 9.423

4.  Rectifying RNA splicing errors in hereditary neurodegenerative disease.

Authors:  Maurice S Swanson
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-17       Impact factor: 11.205

5.  A subset of SMN complex members have a specific role in tissue regeneration via ERBB pathway-mediated proliferation.

Authors:  Wuhong Pei; Lisha Xu; Zelin Chen; Claire C Slevin; Kade P Pettie; Stephen Wincovitch; Shawn M Burgess
Journal:  NPJ Regen Med       Date:  2020-03-25

Review 6.  Disease mechanisms and therapeutic approaches in spinal muscular atrophy.

Authors:  Sarah Tisdale; Livio Pellizzoni
Journal:  J Neurosci       Date:  2015-06-10       Impact factor: 6.167

7.  SMN deficiency negatively impacts red pulp macrophages and spleen development in mouse models of spinal muscular atrophy.

Authors:  Marie-Therese Khairallah; Jacob Astroski; Sarah K Custer; Elliot J Androphy; Craig L Franklin; Christian L Lorson
Journal:  Hum Mol Genet       Date:  2017-03-01       Impact factor: 6.150

8.  A new communication hub in the RNA world.

Authors:  Megan Mayerle; Christine Guthrie
Journal:  Nat Struct Mol Biol       Date:  2016-03       Impact factor: 15.369

Review 9.  Cajal bodies in neurons.

Authors:  Miguel Lafarga; Olga Tapia; Ana M Romero; Maria T Berciano
Journal:  RNA Biol       Date:  2016-09-14       Impact factor: 4.652

10.  Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals.

Authors:  Ludwig Heesen; Michael Peitz; Laura Torres-Benito; Irmgard Hölker; Kristina Hupperich; Kristina Dobrindt; Johannes Jungverdorben; Swetlana Ritzenhofen; Beatrice Weykopf; Daniela Eckert; Seyyed Mohsen Hosseini-Barkooie; Markus Storbeck; Noemi Fusaki; Renata Lonigro; Raoul Heller; Min Jeong Kye; Oliver Brüstle; Brunhilde Wirth
Journal:  Cell Mol Life Sci       Date:  2015-11-16       Impact factor: 9.261

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.