Literature DB >> 21084389

Developments in RNA splicing and disease.

Michael G Poulos1, Ranjan Batra, Konstantinos Charizanis, Maurice S Swanson.   

Abstract

Pre-mRNA processing, including 5'-end capping, splicing, editing, and polyadenylation, consists of a series of orchestrated and primarily cotranscriptional steps that ensure both the high fidelity and extreme diversity characteristic of eukaryotic gene expression. Alternative splicing and editing allow relatively small genomes to encode vast proteomic arrays while alternative 3'-end formation enables variations in mRNA localization, translation, and stability. Of course, this mechanistic complexity comes at a high price. Mutations in the myriad of RNA sequence elements that regulate mRNA biogenesis, as well as the trans-acting factors that act upon these sequences, underlie a number of human diseases. In this review, we focus on one of these key RNA processing steps, splicing, to highlight recent studies that describe both conventional and novel pathogenic mechanisms that underlie muscle and neurological diseases.

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Year:  2011        PMID: 21084389      PMCID: PMC3003463          DOI: 10.1101/cshperspect.a000778

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  90 in total

1.  Composition and three-dimensional EM structure of double affinity-purified, human prespliceosomal A complexes.

Authors:  Nastaran Behzadnia; Monika M Golas; Klaus Hartmuth; Bjoern Sander; Berthold Kastner; Jochen Deckert; Prakash Dube; Cindy L Will; Henning Urlaub; Holger Stark; Reinhard Lührmann
Journal:  EMBO J       Date:  2007-03-01       Impact factor: 11.598

2.  Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene.

Authors:  Paul J Hagerman; Randi J Hagerman
Journal:  Nat Clin Pract Neurol       Date:  2007-02

Review 3.  Splicing regulation in neurologic disease.

Authors:  Donny D Licatalosi; Robert B Darnell
Journal:  Neuron       Date:  2006-10-05       Impact factor: 17.173

Review 4.  Dystrophin, its interactions with other proteins, and implications for muscular dystrophy.

Authors:  James M Ervasti
Journal:  Biochim Biophys Acta       Date:  2006-06-07

Review 5.  Friedreich ataxia.

Authors:  Massimo Pandolfo
Journal:  Arch Neurol       Date:  2008-10

Review 6.  Facioscapulohumeral muscular dystrophy.

Authors:  Rabi Tawil
Journal:  Neurotherapeutics       Date:  2008-10       Impact factor: 7.620

7.  Antisense masking of an hnRNP A1/A2 intronic splicing silencer corrects SMN2 splicing in transgenic mice.

Authors:  Yimin Hua; Timothy A Vickers; Hazeem L Okunola; C Frank Bennett; Adrian R Krainer
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

8.  Motor coordination defects in mice deficient for the Sam68 RNA-binding protein.

Authors:  Kiven E Lukong; Stéphane Richard
Journal:  Behav Brain Res       Date:  2008-02-05       Impact factor: 3.332

Review 9.  The SMN complex, an assemblyosome of ribonucleoproteins.

Authors:  Sergey Paushkin; Amélie K Gubitz; Séverine Massenet; Gideon Dreyfuss
Journal:  Curr Opin Cell Biol       Date:  2002-06       Impact factor: 8.382

10.  DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy.

Authors:  Olga L Gurvich; Therese M Tuohy; Michael T Howard; Richard S Finkel; Livija Medne; Christine B Anderson; Robert B Weiss; Steve D Wilton; Kevin M Flanigan
Journal:  Ann Neurol       Date:  2008-01       Impact factor: 10.422

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  43 in total

Review 1.  Neurodegeneration the RNA way.

Authors:  Abigail J Renoux; Peter K Todd
Journal:  Prog Neurobiol       Date:  2011-11-03       Impact factor: 11.685

2.  A novel FADS1 isoform potentiates FADS2-mediated production of eicosanoid precursor fatty acids.

Authors:  Woo Jung Park; Kumar S D Kothapalli; Holly T Reardon; Peter Lawrence; Shu-Bing Qian; J Thomas Brenna
Journal:  J Lipid Res       Date:  2012-05-22       Impact factor: 5.922

Review 3.  RNA protein interaction in neurons.

Authors:  Robert B Darnell
Journal:  Annu Rev Neurosci       Date:  2013-05-20       Impact factor: 12.449

Review 4.  Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders.

Authors:  John Douglas Cleary; Laura P W Ranum
Journal:  Curr Opin Genet Dev       Date:  2014-05-22       Impact factor: 5.578

5.  The intracerebral hemorrhage blood transcriptome in humans differs from the ischemic stroke and vascular risk factor control blood transcriptomes.

Authors:  Boryana Stamova; Bradley P Ander; Glen Jickling; Farah Hamade; Marc Durocher; Xinhua Zhan; Da Zhi Liu; Xiyuan Cheng; Heather Hull; Alan Yee; Kwan Ng; Natasha Shroff; Frank R Sharp
Journal:  J Cereb Blood Flow Metab       Date:  2018-04-13       Impact factor: 6.200

6.  Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease.

Authors:  Ranjan Batra; Konstantinos Charizanis; Mini Manchanda; Apoorva Mohan; Moyi Li; Dustin J Finn; Marianne Goodwin; Chaolin Zhang; Krzysztof Sobczak; Charles A Thornton; Maurice S Swanson
Journal:  Mol Cell       Date:  2014-09-25       Impact factor: 17.970

7.  Global insights into alternative polyadenylation regulation.

Authors:  Ranjan Batra; Mini Manchanda; Maurice S Swanson
Journal:  RNA Biol       Date:  2015       Impact factor: 4.652

8.  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

9.  Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise.

Authors:  Christopher M Chamberlain; Laura P W Ranum
Journal:  Hum Mol Genet       Date:  2012-07-30       Impact factor: 6.150

10.  Functional understanding of the diverse exon-intron structures of human GPCR genes.

Authors:  Dorothy A Hammond; Victor Olman; Ying Xu
Journal:  J Bioinform Comput Biol       Date:  2013-12-11       Impact factor: 1.122

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