Literature DB >> 25957814

mRNA metabolism and neuronal disease.

Bastian Linder1, Utz Fischer2, Niels H Gehring3.   

Abstract

To serve as templates for translation eukaryotic mRNAs undergo an elaborate processing and maturation pathway. In eukaryotes this process comprises the synthesis of mRNA precursors, their processing and transport to the site of translation and eventually their decay. During the entire life cycle, mRNAs interact with distinct sets of trans-acting factors that determine their fate at any given phase of gene expression. Recent studies have shown that mutations in components acting in trans on mRNAs are frequent causes of a large variety of different human disorders. The etiology of most of these diseases is, however, only poorly understood, mostly because the consequences for mRNA-metabolism are unclear. Here we discuss three prominent genetic diseases that fall into this category, namely spinal muscular atrophy (SMA), retinitis pigmentosa (RP) and X-linked syndromic mental retardation (XLMR). Whereas SMA and RP can be directly linked to mRNA processing, XLMR results from mutations in the mRNA surveillance system. We discuss how defects in mRNA maturation and turnover might lead to the tissue specific defects seen in these diseases.
Copyright © 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Genetic disease; Post-transcriptional regulation of gene expression; Splicing; mRNA; mRNA turnover

Mesh:

Substances:

Year:  2015        PMID: 25957814     DOI: 10.1016/j.febslet.2015.04.052

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  10 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.  Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in Females.

Authors:  Jennifer M Bain; Megan T Cho; Aida Telegrafi; Ashley Wilson; Susan Brooks; Christina Botti; Gordon Gowans; Leigh Anne Autullo; Vidya Krishnamurthy; Marcia C Willing; Tomi L Toler; Bruria Ben-Zev; Orly Elpeleg; Yufeng Shen; Kyle Retterer; Kristin G Monaghan; Wendy K Chung
Journal:  Am J Hum Genet       Date:  2016-08-18       Impact factor: 11.025

3.  Mapping transcriptome-wide protein-RNA interactions to elucidate RNA regulatory programs.

Authors:  Molly M Hannigan; Leah L Zagore; Donny D Licatalosi
Journal:  Quant Biol       Date:  2018-07-27

4.  Distinguishing Alzheimer's Disease Patients and Biochemical Phenotype Analysis Using a Novel Serum Profiling Platform: Potential Involvement of the VWF/ADAMTS13 Axis.

Authors:  Jay S Hanas; James R S Hocker; Christian A Vannarath; Megan R Lerner; Scott G Blair; Stan A Lightfoot; Rushie J Hanas; James R Couch; Linda A Hershey
Journal:  Brain Sci       Date:  2021-04-30

Review 5.  The RNA exosome and RNA exosome-linked disease.

Authors:  Derrick J Morton; Emily G Kuiper; Stephanie K Jones; Sara W Leung; Anita H Corbett; Milo B Fasken
Journal:  RNA       Date:  2017-11-01       Impact factor: 4.942

Review 6.  Mutations in spliceosomal proteins and retina degeneration.

Authors:  Šárka Růžičková; David Staněk
Journal:  RNA Biol       Date:  2016-06-14       Impact factor: 4.652

7.  Identification and characterization of functional modules reflecting transcriptome transition during human neuron maturation.

Authors:  Zhisong He; Qianhui Yu
Journal:  BMC Genomics       Date:  2018-04-17       Impact factor: 3.969

8.  Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder.

Authors:  Jennifer M Bain; Olivia Thornburg; Cheryl Pan; Donnielle Rome-Martin; Lia Boyle; Xiao Fan; Orrin Devinsky; Richard Frye; Silke Hamp; Cynthia G Keator; Nicole M LaMarca; Alexis B R Maddocks; Marcos Madruga-Garrido; Karen Y Niederhoffer; Francesca Novara; Angela Peron; Elizabeth Poole-Di Salvo; Rachel Salazar; Steven A Skinner; Gabriela Soares; Sylvie Goldman; Wendy K Chung
Journal:  Neurol Genet       Date:  2021-01-29

9.  Dual function of UPF3B in early and late translation termination.

Authors:  Gabriele Neu-Yilik; Etienne Raimondeau; Boris Eliseev; Lahari Yeramala; Beate Amthor; Aurélien Deniaud; Karine Huard; Kathrin Kerschgens; Matthias W Hentze; Christiane Schaffitzel; Andreas E Kulozik
Journal:  EMBO J       Date:  2017-09-12       Impact factor: 11.598

10.  Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease.

Authors:  Alexa Derksen; Hung-Yu Shih; Diane Forget; Lama Darbelli; Luan T Tran; Christian Poitras; Kether Guerrero; Sundaresan Tharun; Fowzan S Alkuraya; Wesam I Kurdi; Cam-Tu Emilie Nguyen; Anne-Marie Laberge; Yue Si; Marie-Soleil Gauthier; Joshua L Bonkowsky; Benoit Coulombe; Geneviève Bernard
Journal:  HGG Adv       Date:  2021-05-05
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.